Other mutations in this stock |
Total: 223 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930447A16Rik |
G |
A |
15: 37,439,844 (GRCm39) |
|
probably benign |
Het |
Aadat |
A |
G |
8: 60,979,746 (GRCm39) |
T203A |
probably damaging |
Het |
Abca13 |
T |
A |
11: 9,199,680 (GRCm39) |
F104L |
probably benign |
Het |
Acox1 |
T |
A |
11: 116,089,109 (GRCm39) |
|
probably null |
Het |
Adam34l |
T |
C |
8: 44,078,620 (GRCm39) |
N535D |
probably damaging |
Het |
Adamts17 |
C |
T |
7: 66,799,704 (GRCm39) |
R1060* |
probably null |
Het |
Adgrg6 |
T |
C |
10: 14,315,526 (GRCm39) |
T593A |
probably damaging |
Het |
Ankrd12 |
G |
T |
17: 66,291,071 (GRCm39) |
P1454Q |
probably benign |
Het |
Ap2m1 |
T |
A |
16: 20,358,088 (GRCm39) |
N35K |
probably damaging |
Het |
Aspm |
A |
G |
1: 139,401,312 (GRCm39) |
I1111V |
probably benign |
Het |
Atr |
G |
A |
9: 95,779,634 (GRCm39) |
V1331I |
probably benign |
Het |
Bola1 |
C |
T |
3: 96,104,426 (GRCm39) |
G56D |
probably benign |
Het |
Brsk1 |
A |
G |
7: 4,707,218 (GRCm39) |
D257G |
probably damaging |
Het |
C4bp |
C |
G |
1: 130,570,725 (GRCm39) |
V284L |
probably benign |
Het |
Cacna1s |
T |
C |
1: 136,046,454 (GRCm39) |
F1761S |
probably benign |
Het |
Camsap2 |
C |
T |
1: 136,209,053 (GRCm39) |
R802Q |
probably benign |
Het |
Cbs |
G |
T |
17: 31,839,923 (GRCm39) |
A337E |
probably benign |
Het |
Ccdc186 |
A |
C |
19: 56,797,652 (GRCm39) |
H306Q |
probably benign |
Het |
Ccdc93 |
T |
C |
1: 121,389,668 (GRCm39) |
V237A |
probably benign |
Het |
Ccdc93 |
C |
T |
1: 121,383,855 (GRCm39) |
P192L |
probably benign |
Het |
Cd55 |
C |
T |
1: 130,377,160 (GRCm39) |
V333I |
probably benign |
Het |
Cd55 |
C |
A |
1: 130,387,370 (GRCm39) |
A143S |
probably benign |
Het |
Cdh19 |
C |
A |
1: 110,821,114 (GRCm39) |
E541D |
probably damaging |
Het |
Cdh20 |
C |
G |
1: 109,993,465 (GRCm39) |
L307V |
possibly damaging |
Het |
Cfh |
C |
T |
1: 140,075,435 (GRCm39) |
V268I |
possibly damaging |
Het |
Cfhr2 |
A |
G |
1: 139,741,180 (GRCm39) |
M265T |
probably benign |
Het |
Cfhr2 |
A |
C |
1: 139,741,197 (GRCm39) |
N259K |
probably benign |
Het |
Chi3l1 |
C |
T |
1: 134,116,267 (GRCm39) |
A250V |
probably damaging |
Het |
Chrnb1 |
C |
A |
11: 69,676,588 (GRCm39) |
D388Y |
probably damaging |
Het |
Clcn1 |
T |
A |
6: 42,276,448 (GRCm39) |
F360Y |
possibly damaging |
Het |
Clgn |
A |
G |
8: 84,149,659 (GRCm39) |
S387G |
probably damaging |
Het |
Cntnap5a |
C |
T |
1: 116,382,873 (GRCm39) |
T1047I |
probably benign |
Het |
Cntnap5a |
C |
A |
1: 116,382,734 (GRCm39) |
L1001I |
probably benign |
Het |
Cntnap5a |
T |
C |
1: 116,382,831 (GRCm39) |
L1033S |
probably benign |
Het |
Coil |
G |
A |
11: 88,864,802 (GRCm39) |
V10I |
probably damaging |
Het |
Col4a1 |
G |
A |
8: 11,262,712 (GRCm39) |
P1256S |
possibly damaging |
Het |
Copa |
T |
A |
1: 171,939,554 (GRCm39) |
F597Y |
probably benign |
Het |
Crb1 |
G |
A |
1: 139,168,876 (GRCm39) |
P881S |
probably damaging |
Het |
Crb1 |
C |
T |
1: 139,170,733 (GRCm39) |
G825R |
probably damaging |
Het |
Crb1 |
C |
T |
1: 139,171,155 (GRCm39) |
R684H |
probably benign |
Het |
Crb1 |
T |
C |
1: 139,162,517 (GRCm39) |
M1214V |
probably benign |
Het |
Crb1 |
A |
T |
1: 139,165,360 (GRCm39) |
H921Q |
probably benign |
Het |
Crybg1 |
T |
A |
10: 43,880,015 (GRCm39) |
Q391L |
probably damaging |
Het |
Cspg4 |
G |
T |
9: 56,805,821 (GRCm39) |
V2211L |
probably benign |
Het |
Cxcr4 |
C |
T |
1: 128,517,014 (GRCm39) |
V216I |
probably benign |
Het |
Cyb5r1 |
C |
T |
1: 134,335,405 (GRCm39) |
R147W |
probably damaging |
Het |
Ddx59 |
T |
C |
1: 136,344,791 (GRCm39) |
V154A |
probably benign |
Het |
Dhx30 |
T |
C |
9: 109,927,819 (GRCm39) |
H101R |
probably damaging |
Het |
Dnah11 |
T |
A |
12: 117,880,666 (GRCm39) |
D3818V |
probably damaging |
Het |
Dnah17 |
C |
T |
11: 117,960,345 (GRCm39) |
C2572Y |
possibly damaging |
Het |
Dsel |
T |
C |
1: 111,787,187 (GRCm39) |
N1116S |
probably benign |
Het |
Dsel |
G |
C |
1: 111,787,724 (GRCm39) |
T937S |
probably benign |
Het |
Dstyk |
C |
T |
1: 132,384,722 (GRCm39) |
L739F |
probably damaging |
Het |
Ehf |
T |
G |
2: 103,104,251 (GRCm39) |
T186P |
possibly damaging |
Het |
En1 |
A |
G |
1: 120,531,350 (GRCm39) |
S197G |
unknown |
Het |
Etnk2 |
C |
A |
1: 133,293,325 (GRCm39) |
D89E |
probably benign |
Het |
Etnk2 |
G |
T |
1: 133,293,503 (GRCm39) |
G149W |
probably damaging |
Het |
Etnk2 |
C |
T |
1: 133,293,554 (GRCm39) |
R166* |
probably null |
Het |
Etnk2 |
G |
A |
1: 133,293,555 (GRCm39) |
R166Q |
probably benign |
Het |
Etnk2 |
T |
A |
1: 133,304,653 (GRCm39) |
V292E |
probably benign |
Het |
Fam187b |
C |
T |
7: 30,688,445 (GRCm39) |
Q268* |
probably null |
Het |
Fam72a |
C |
T |
1: 131,466,633 (GRCm39) |
T139M |
probably benign |
Het |
Fam72a |
T |
C |
1: 131,458,406 (GRCm39) |
I56T |
probably benign |
Het |
Fat3 |
A |
C |
9: 15,907,611 (GRCm39) |
V2797G |
possibly damaging |
Het |
Fcamr |
A |
C |
1: 130,732,364 (GRCm39) |
N117T |
probably benign |
Het |
Fcamr |
A |
G |
1: 130,739,317 (GRCm39) |
I206V |
probably benign |
Het |
Fcamr |
G |
A |
1: 130,740,366 (GRCm39) |
G262S |
probably benign |
Het |
Fcamr |
A |
G |
1: 130,740,429 (GRCm39) |
I283V |
probably benign |
Het |
Fcamr |
T |
C |
1: 130,740,475 (GRCm39) |
V298A |
probably benign |
Het |
Fcamr |
A |
G |
1: 130,740,546 (GRCm39) |
M322V |
probably benign |
Het |
Fcamr |
C |
T |
1: 130,740,553 (GRCm39) |
P324L |
probably benign |
Het |
Fcamr |
A |
G |
1: 130,742,334 (GRCm39) |
N574D |
probably benign |
Het |
Fcamr |
A |
G |
1: 130,732,306 (GRCm39) |
R98G |
probably benign |
Het |
Fcmr |
T |
C |
1: 130,806,006 (GRCm39) |
S321P |
probably benign |
Het |
Fcmr |
A |
G |
1: 130,803,711 (GRCm39) |
T172A |
probably benign |
Het |
Fut10 |
T |
A |
8: 31,691,418 (GRCm39) |
S88T |
probably benign |
Het |
Gabarap |
C |
T |
11: 69,882,515 (GRCm39) |
|
probably benign |
Het |
Gli2 |
G |
T |
1: 118,929,774 (GRCm39) |
H44Q |
probably benign |
Het |
Gli2 |
C |
T |
1: 118,795,817 (GRCm39) |
A113T |
possibly damaging |
Het |
Glrx2 |
C |
T |
1: 143,615,478 (GRCm39) |
A27V |
possibly damaging |
Het |
Gm28040 |
AGTG |
AGTGGCACCTTTGGTG |
1: 133,255,059 (GRCm39) |
|
probably benign |
Het |
Gpr25 |
G |
A |
1: 136,188,448 (GRCm39) |
P55L |
probably benign |
Het |
Gse1 |
G |
A |
8: 121,294,992 (GRCm39) |
|
probably benign |
Het |
Heatr4 |
T |
C |
12: 84,014,346 (GRCm39) |
I630M |
probably benign |
Het |
Hectd4 |
A |
T |
5: 121,439,902 (GRCm39) |
Y1134F |
possibly damaging |
Het |
Igfn1 |
G |
A |
1: 135,887,666 (GRCm39) |
P2466L |
probably damaging |
Het |
Igfn1 |
C |
T |
1: 135,899,865 (GRCm39) |
R482Q |
probably benign |
Het |
Igfn1 |
T |
C |
1: 135,898,149 (GRCm39) |
S806G |
probably benign |
Het |
Igfn1 |
G |
A |
1: 135,895,937 (GRCm39) |
A1543V |
probably benign |
Het |
Igfn1 |
C |
T |
1: 135,907,653 (GRCm39) |
A231T |
probably benign |
Het |
Igfn1 |
G |
A |
1: 135,910,213 (GRCm39) |
R124W |
probably benign |
Het |
Igfn1 |
T |
C |
1: 135,926,363 (GRCm39) |
E29G |
probably benign |
Het |
Igfn1 |
T |
C |
1: 135,926,421 (GRCm39) |
I10V |
unknown |
Het |
Ikbke |
T |
C |
1: 131,197,560 (GRCm39) |
S447G |
probably benign |
Het |
Ikbke |
C |
A |
1: 131,193,674 (GRCm39) |
A459S |
probably benign |
Het |
Ildr1 |
A |
T |
16: 36,528,698 (GRCm39) |
T48S |
possibly damaging |
Het |
Ipo9 |
ATCCTCCTCCTCCTCCTC |
ATCCTCCTCCTCCTCCTCCTC |
1: 135,314,006 (GRCm39) |
|
probably benign |
Het |
Ipo9 |
A |
G |
1: 135,329,988 (GRCm39) |
V484A |
probably benign |
Het |
Ipo9 |
CTC |
CTCTTC |
1: 135,314,009 (GRCm39) |
|
probably benign |
Het |
Itprid1 |
T |
C |
6: 55,945,526 (GRCm39) |
F749S |
probably benign |
Het |
Jarid2 |
T |
A |
13: 45,059,752 (GRCm39) |
N661K |
probably damaging |
Het |
Kcnh5 |
T |
C |
12: 75,184,465 (GRCm39) |
D86G |
probably benign |
Het |
Kcnt2 |
G |
A |
1: 140,282,285 (GRCm39) |
S90N |
probably benign |
Het |
Kif14 |
A |
G |
1: 136,396,713 (GRCm39) |
K340E |
probably damaging |
Het |
Kif14 |
G |
A |
1: 136,406,103 (GRCm39) |
A556T |
probably benign |
Het |
Kif14 |
A |
G |
1: 136,418,070 (GRCm39) |
S868G |
probably benign |
Het |
Kif14 |
C |
T |
1: 136,431,169 (GRCm39) |
L1189F |
probably benign |
Het |
Kif14 |
T |
C |
1: 136,443,699 (GRCm39) |
F1291L |
probably benign |
Het |
Kif14 |
T |
C |
1: 136,453,521 (GRCm39) |
V1433A |
probably benign |
Het |
Kif14 |
A |
G |
1: 136,396,017 (GRCm39) |
N108D |
probably benign |
Het |
Kif1b |
T |
C |
4: 149,272,179 (GRCm39) |
T1541A |
probably damaging |
Het |
Kif21b |
A |
G |
1: 136,087,859 (GRCm39) |
I983V |
possibly damaging |
Het |
Kif26a |
T |
C |
12: 112,143,219 (GRCm39) |
S1158P |
possibly damaging |
Het |
Kmt2d |
A |
G |
15: 98,763,013 (GRCm39) |
C279R |
probably damaging |
Het |
Kpna3 |
T |
A |
14: 61,605,150 (GRCm39) |
E499V |
probably benign |
Het |
Krt16 |
T |
C |
11: 100,138,533 (GRCm39) |
E205G |
probably damaging |
Het |
Lad1 |
C |
T |
1: 135,755,761 (GRCm39) |
R346C |
probably damaging |
Het |
Lad1 |
C |
T |
1: 135,755,119 (GRCm39) |
P132S |
possibly damaging |
Het |
Lax1 |
T |
C |
1: 133,608,307 (GRCm39) |
N145D |
probably benign |
Het |
Lax1 |
G |
A |
1: 133,611,372 (GRCm39) |
P67S |
probably damaging |
Het |
Lax1 |
T |
C |
1: 133,607,716 (GRCm39) |
R342G |
probably benign |
Het |
Lgr6 |
C |
T |
1: 134,914,826 (GRCm39) |
V641I |
probably benign |
Het |
Lgr6 |
G |
T |
1: 134,918,373 (GRCm39) |
H263N |
probably benign |
Het |
Lgr6 |
C |
T |
1: 134,931,214 (GRCm39) |
S3N |
probably benign |
Het |
Lmod1 |
C |
T |
1: 135,291,811 (GRCm39) |
T222I |
probably benign |
Het |
Mb21d2 |
A |
G |
16: 28,647,173 (GRCm39) |
V267A |
probably benign |
Het |
Mfrp |
A |
G |
9: 44,015,884 (GRCm39) |
T334A |
possibly damaging |
Het |
Morc1 |
T |
A |
16: 48,432,660 (GRCm39) |
D709E |
probably benign |
Het |
Mrgpra2b |
A |
G |
7: 47,114,627 (GRCm39) |
I35T |
probably benign |
Het |
Mroh3 |
G |
C |
1: 136,119,882 (GRCm39) |
Q440E |
possibly damaging |
Het |
Mybph |
C |
T |
1: 134,125,218 (GRCm39) |
R249C |
probably benign |
Het |
Mycbp2 |
A |
T |
14: 103,392,614 (GRCm39) |
C3206S |
probably damaging |
Het |
Nav1 |
A |
T |
1: 135,512,465 (GRCm39) |
D198E |
possibly damaging |
Het |
Ndufaf7 |
A |
T |
17: 79,245,058 (GRCm39) |
K59M |
probably damaging |
Het |
Necab3 |
T |
C |
2: 154,388,795 (GRCm39) |
S208G |
probably benign |
Het |
Nr5a2 |
C |
A |
1: 136,879,863 (GRCm39) |
R35L |
probably benign |
Het |
Obsl1 |
G |
A |
1: 75,486,756 (GRCm38) |
T1764M |
probably benign |
Het |
Optc |
A |
T |
1: 133,831,534 (GRCm39) |
|
probably null |
Het |
Optc |
C |
G |
1: 133,832,908 (GRCm39) |
S64T |
probably benign |
Het |
Or2f1 |
C |
A |
6: 42,721,069 (GRCm39) |
L33M |
possibly damaging |
Het |
Or3a1c |
A |
G |
11: 74,046,802 (GRCm39) |
D274G |
probably damaging |
Het |
Or4a68 |
C |
T |
2: 89,269,927 (GRCm39) |
R232H |
probably benign |
Het |
Or5m13b |
T |
A |
2: 85,754,466 (GRCm39) |
L285I |
possibly damaging |
Het |
Or8b12i |
A |
T |
9: 20,082,209 (GRCm39) |
Y219* |
probably null |
Het |
Otoa |
T |
C |
7: 120,724,662 (GRCm39) |
V447A |
probably benign |
Het |
Papss1 |
A |
G |
3: 131,311,728 (GRCm39) |
N319D |
probably benign |
Het |
Patj |
G |
A |
4: 98,320,017 (GRCm39) |
G428D |
possibly damaging |
Het |
Pcdhb3 |
G |
A |
18: 37,434,931 (GRCm39) |
G299D |
probably damaging |
Het |
Pcsk4 |
T |
C |
10: 80,159,404 (GRCm39) |
D432G |
probably damaging |
Het |
Pde5a |
G |
T |
3: 122,541,889 (GRCm39) |
L126F |
probably damaging |
Het |
Pigr |
C |
T |
1: 130,772,259 (GRCm39) |
A159V |
possibly damaging |
Het |
Pik3c2b |
C |
T |
1: 132,994,365 (GRCm39) |
P110S |
probably benign |
Het |
Pinx1 |
A |
G |
14: 64,115,559 (GRCm39) |
|
probably null |
Het |
Plec |
C |
A |
15: 76,061,892 (GRCm39) |
E2547* |
probably null |
Het |
Plekha6 |
C |
G |
1: 133,215,584 (GRCm39) |
T792S |
probably benign |
Het |
Ppfia4 |
G |
A |
1: 134,227,059 (GRCm39) |
P1159S |
probably benign |
Het |
Prelp |
C |
T |
1: 133,842,869 (GRCm39) |
R92K |
probably benign |
Het |
Prrx1 |
T |
A |
1: 163,089,536 (GRCm39) |
N97I |
probably damaging |
Het |
Ptpn7 |
A |
G |
1: 135,062,213 (GRCm39) |
Q53R |
probably benign |
Het |
Ptprc |
A |
G |
1: 138,035,575 (GRCm39) |
V400A |
probably benign |
Het |
Ptprc |
C |
A |
1: 138,035,562 (GRCm39) |
E402D |
probably benign |
Het |
Ptprc |
A |
G |
1: 138,035,561 (GRCm39) |
S405P |
probably benign |
Het |
Ptprc |
T |
G |
1: 138,027,414 (GRCm39) |
N478T |
probably benign |
Het |
Ptprc |
T |
C |
1: 138,039,992 (GRCm39) |
K212E |
possibly damaging |
Het |
Rab29 |
A |
G |
1: 131,799,848 (GRCm39) |
Q141R |
probably benign |
Het |
Rbsn |
A |
T |
6: 92,167,000 (GRCm39) |
L548Q |
possibly damaging |
Het |
Ren1 |
C |
T |
1: 133,281,975 (GRCm39) |
T32I |
probably benign |
Het |
Ren1 |
T |
A |
1: 133,281,944 (GRCm39) |
W22R |
probably damaging |
Het |
Ren1 |
C |
G |
1: 133,287,745 (GRCm39) |
L360V |
probably benign |
Het |
Ren1 |
A |
T |
1: 133,287,721 (GRCm39) |
N352Y |
probably benign |
Het |
Ren1 |
A |
T |
1: 133,286,817 (GRCm39) |
E315D |
probably benign |
Het |
Ren1 |
C |
A |
1: 133,286,720 (GRCm39) |
|
probably null |
Het |
Ren1 |
A |
C |
1: 133,284,195 (GRCm39) |
K187Q |
probably benign |
Het |
Rnpep |
C |
T |
1: 135,190,834 (GRCm39) |
A571T |
possibly damaging |
Het |
Rnpep |
G |
C |
1: 135,211,715 (GRCm39) |
A11G |
probably benign |
Het |
Ro60 |
T |
C |
1: 143,635,772 (GRCm39) |
D458G |
probably benign |
Het |
Ro60 |
C |
T |
1: 143,635,752 (GRCm39) |
V465I |
probably benign |
Het |
Sctr |
G |
A |
1: 119,990,987 (GRCm39) |
S440N |
possibly damaging |
Het |
Sctr |
T |
C |
1: 119,959,386 (GRCm39) |
F110L |
probably benign |
Het |
Serpinb10 |
C |
T |
1: 107,466,203 (GRCm39) |
S63F |
probably damaging |
Het |
Serpinb2 |
G |
A |
1: 107,443,365 (GRCm39) |
A55T |
probably damaging |
Het |
Serpinb2 |
A |
C |
1: 107,452,273 (GRCm39) |
S284R |
probably benign |
Het |
Serpinb2 |
C |
T |
1: 107,451,624 (GRCm39) |
T259I |
probably benign |
Het |
Serpinb2 |
C |
T |
1: 107,451,620 (GRCm39) |
H258Y |
probably benign |
Het |
Serpinb2 |
C |
A |
1: 107,451,564 (GRCm39) |
A239E |
probably benign |
Het |
Serpinb8 |
A |
G |
1: 107,525,257 (GRCm39) |
S20G |
probably benign |
Het |
Serpinb8 |
A |
C |
1: 107,534,734 (GRCm39) |
L268F |
probably benign |
Het |
Serpinb8 |
G |
A |
1: 107,526,684 (GRCm39) |
A75T |
probably benign |
Het |
Sis |
A |
T |
3: 72,872,978 (GRCm39) |
C53* |
probably null |
Het |
Slc13a5 |
C |
T |
11: 72,157,285 (GRCm39) |
|
probably null |
Het |
Slc26a9 |
C |
T |
1: 131,691,608 (GRCm39) |
A617V |
probably benign |
Het |
Slc26a9 |
C |
A |
1: 131,693,750 (GRCm39) |
R747S |
probably benign |
Het |
Slc9a8 |
T |
C |
2: 167,266,065 (GRCm39) |
F14S |
probably benign |
Het |
Spock3 |
T |
C |
8: 63,802,011 (GRCm39) |
L330P |
probably damaging |
Het |
Stab2 |
T |
G |
10: 86,773,903 (GRCm39) |
R809S |
probably benign |
Het |
Steap3 |
G |
A |
1: 120,162,108 (GRCm39) |
A350V |
probably benign |
Het |
Steap3 |
T |
C |
1: 120,155,480 (GRCm39) |
N493S |
probably benign |
Het |
Tecta |
G |
A |
9: 42,303,218 (GRCm39) |
T138I |
probably benign |
Het |
Thsd7b |
G |
C |
1: 129,605,920 (GRCm39) |
A554P |
probably benign |
Het |
Thsd7b |
A |
C |
1: 130,044,368 (GRCm39) |
Q1116P |
probably benign |
Het |
Thsd7b |
C |
T |
1: 129,556,628 (GRCm39) |
T328I |
probably damaging |
Het |
Thsd7b |
T |
A |
1: 129,595,674 (GRCm39) |
F498Y |
probably benign |
Het |
Tnnt2 |
C |
T |
1: 135,773,244 (GRCm39) |
|
probably benign |
Het |
Traf7 |
A |
G |
17: 24,731,353 (GRCm39) |
F228L |
probably damaging |
Het |
Trhr |
A |
G |
15: 44,060,549 (GRCm39) |
E23G |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,643,683 (GRCm39) |
G11436R |
probably damaging |
Het |
Tubgcp2 |
T |
C |
7: 139,577,968 (GRCm39) |
T779A |
probably benign |
Het |
Tusc2 |
A |
T |
9: 107,441,830 (GRCm39) |
I68F |
probably damaging |
Het |
Ube2t |
C |
T |
1: 134,899,905 (GRCm39) |
A149V |
probably benign |
Het |
Upf2 |
A |
T |
2: 6,032,261 (GRCm39) |
S191C |
probably damaging |
Het |
Usp24 |
A |
G |
4: 106,217,618 (GRCm39) |
N447S |
possibly damaging |
Het |
Usp42 |
T |
C |
5: 143,700,381 (GRCm39) |
D1214G |
probably damaging |
Het |
Vcam1 |
T |
A |
3: 115,908,164 (GRCm39) |
I633L |
probably benign |
Het |
Vmn2r73 |
T |
C |
7: 85,507,086 (GRCm39) |
Y742C |
probably damaging |
Het |
Vmn2r81 |
C |
A |
10: 79,106,489 (GRCm39) |
T489K |
probably benign |
Het |
Ypel1 |
C |
G |
16: 16,907,283 (GRCm39) |
|
probably benign |
Het |
Zan |
C |
A |
5: 137,413,280 (GRCm39) |
|
probably benign |
Het |
Zc3h11a |
C |
T |
1: 133,552,359 (GRCm39) |
V583I |
probably benign |
Het |
Zc3h11a |
G |
A |
1: 133,549,892 (GRCm39) |
P695S |
probably benign |
Het |
Zfp616 |
A |
C |
11: 73,976,597 (GRCm39) |
K955N |
probably damaging |
Het |
Zfyve9 |
A |
C |
4: 108,575,698 (GRCm39) |
V461G |
possibly damaging |
Het |
Zp3r |
A |
G |
1: 130,524,551 (GRCm39) |
L164P |
probably benign |
Het |
Zp3r |
C |
A |
1: 130,547,151 (GRCm39) |
E8D |
possibly damaging |
Het |
|
Other mutations in Ryr2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00518:Ryr2
|
APN |
13 |
11,848,978 (GRCm39) |
splice site |
probably benign |
|
IGL00757:Ryr2
|
APN |
13 |
11,633,490 (GRCm39) |
splice site |
probably null |
|
IGL00838:Ryr2
|
APN |
13 |
11,583,389 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00849:Ryr2
|
APN |
13 |
11,600,364 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL00987:Ryr2
|
APN |
13 |
11,750,388 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01096:Ryr2
|
APN |
13 |
11,718,430 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01313:Ryr2
|
APN |
13 |
11,653,371 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL01349:Ryr2
|
APN |
13 |
11,602,125 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01391:Ryr2
|
APN |
13 |
11,571,571 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL01401:Ryr2
|
APN |
13 |
11,606,238 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL01412:Ryr2
|
APN |
13 |
11,756,922 (GRCm39) |
missense |
probably benign |
0.10 |
IGL01419:Ryr2
|
APN |
13 |
11,814,723 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL01432:Ryr2
|
APN |
13 |
11,866,090 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL01533:Ryr2
|
APN |
13 |
11,736,676 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01571:Ryr2
|
APN |
13 |
11,736,647 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01584:Ryr2
|
APN |
13 |
11,616,644 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01611:Ryr2
|
APN |
13 |
11,606,202 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL01632:Ryr2
|
APN |
13 |
11,609,854 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01643:Ryr2
|
APN |
13 |
11,707,563 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01647:Ryr2
|
APN |
13 |
11,600,366 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01730:Ryr2
|
APN |
13 |
11,616,728 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL01834:Ryr2
|
APN |
13 |
11,610,311 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL01921:Ryr2
|
APN |
13 |
11,569,436 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL01937:Ryr2
|
APN |
13 |
11,805,249 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01945:Ryr2
|
APN |
13 |
11,805,249 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02027:Ryr2
|
APN |
13 |
11,611,998 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02060:Ryr2
|
APN |
13 |
11,762,450 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02065:Ryr2
|
APN |
13 |
11,587,143 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02084:Ryr2
|
APN |
13 |
11,807,648 (GRCm39) |
nonsense |
probably null |
|
IGL02086:Ryr2
|
APN |
13 |
11,750,442 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02095:Ryr2
|
APN |
13 |
11,774,645 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02100:Ryr2
|
APN |
13 |
11,752,759 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02122:Ryr2
|
APN |
13 |
11,756,755 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02202:Ryr2
|
APN |
13 |
11,745,274 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02202:Ryr2
|
APN |
13 |
11,762,544 (GRCm39) |
splice site |
probably benign |
|
IGL02369:Ryr2
|
APN |
13 |
11,634,382 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL02383:Ryr2
|
APN |
13 |
11,737,607 (GRCm39) |
splice site |
probably benign |
|
IGL02400:Ryr2
|
APN |
13 |
11,620,130 (GRCm39) |
splice site |
probably benign |
|
IGL02423:Ryr2
|
APN |
13 |
11,760,084 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02425:Ryr2
|
APN |
13 |
11,760,560 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02458:Ryr2
|
APN |
13 |
11,720,585 (GRCm39) |
missense |
probably benign |
0.15 |
IGL02602:Ryr2
|
APN |
13 |
11,569,397 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02694:Ryr2
|
APN |
13 |
11,620,075 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02726:Ryr2
|
APN |
13 |
11,753,206 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02747:Ryr2
|
APN |
13 |
11,670,563 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02795:Ryr2
|
APN |
13 |
11,610,076 (GRCm39) |
missense |
probably benign |
0.21 |
IGL02876:Ryr2
|
APN |
13 |
11,722,679 (GRCm39) |
missense |
probably benign |
0.39 |
IGL02878:Ryr2
|
APN |
13 |
11,933,205 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02887:Ryr2
|
APN |
13 |
11,606,155 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02926:Ryr2
|
APN |
13 |
11,774,721 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03030:Ryr2
|
APN |
13 |
11,699,365 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03064:Ryr2
|
APN |
13 |
11,658,788 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL03102:Ryr2
|
APN |
13 |
11,650,468 (GRCm39) |
splice site |
probably benign |
|
IGL03152:Ryr2
|
APN |
13 |
11,868,036 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03176:Ryr2
|
APN |
13 |
11,756,909 (GRCm39) |
nonsense |
probably null |
|
IGL03180:Ryr2
|
APN |
13 |
11,583,449 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03213:Ryr2
|
APN |
13 |
11,739,273 (GRCm39) |
splice site |
probably benign |
|
IGL03390:Ryr2
|
APN |
13 |
11,787,302 (GRCm39) |
missense |
probably benign |
|
IGL03410:Ryr2
|
APN |
13 |
11,603,033 (GRCm39) |
missense |
probably damaging |
0.99 |
Arruda
|
UTSW |
13 |
11,658,781 (GRCm39) |
missense |
probably damaging |
1.00 |
Arruda2
|
UTSW |
13 |
11,894,382 (GRCm39) |
missense |
probably damaging |
1.00 |
Arruda3
|
UTSW |
13 |
11,570,334 (GRCm39) |
missense |
possibly damaging |
0.91 |
barricuda
|
UTSW |
13 |
11,609,900 (GRCm39) |
missense |
probably benign |
0.06 |
BB006:Ryr2
|
UTSW |
13 |
11,705,181 (GRCm39) |
nonsense |
probably null |
|
BB006:Ryr2
|
UTSW |
13 |
11,609,680 (GRCm39) |
missense |
probably damaging |
1.00 |
BB016:Ryr2
|
UTSW |
13 |
11,705,181 (GRCm39) |
nonsense |
probably null |
|
BB016:Ryr2
|
UTSW |
13 |
11,609,680 (GRCm39) |
missense |
probably damaging |
1.00 |
H8562:Ryr2
|
UTSW |
13 |
11,732,027 (GRCm39) |
splice site |
probably benign |
|
IGL02799:Ryr2
|
UTSW |
13 |
11,680,848 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02991:Ryr2
|
UTSW |
13 |
11,776,192 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4142001:Ryr2
|
UTSW |
13 |
11,722,682 (GRCm39) |
missense |
probably damaging |
0.97 |
PIT4260001:Ryr2
|
UTSW |
13 |
11,609,641 (GRCm39) |
missense |
possibly damaging |
0.93 |
PIT4458001:Ryr2
|
UTSW |
13 |
11,570,334 (GRCm39) |
missense |
probably benign |
0.29 |
R0003:Ryr2
|
UTSW |
13 |
11,839,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R0004:Ryr2
|
UTSW |
13 |
11,680,805 (GRCm39) |
missense |
probably benign |
|
R0018:Ryr2
|
UTSW |
13 |
11,610,109 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0048:Ryr2
|
UTSW |
13 |
11,610,670 (GRCm39) |
missense |
probably damaging |
1.00 |
R0048:Ryr2
|
UTSW |
13 |
11,610,670 (GRCm39) |
missense |
probably damaging |
1.00 |
R0056:Ryr2
|
UTSW |
13 |
11,683,924 (GRCm39) |
missense |
probably damaging |
0.97 |
R0062:Ryr2
|
UTSW |
13 |
11,884,002 (GRCm39) |
critical splice donor site |
probably null |
|
R0062:Ryr2
|
UTSW |
13 |
11,884,002 (GRCm39) |
critical splice donor site |
probably null |
|
R0080:Ryr2
|
UTSW |
13 |
11,583,361 (GRCm39) |
missense |
probably damaging |
0.98 |
R0116:Ryr2
|
UTSW |
13 |
11,724,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R0148:Ryr2
|
UTSW |
13 |
11,729,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R0206:Ryr2
|
UTSW |
13 |
11,691,137 (GRCm39) |
splice site |
probably benign |
|
R0226:Ryr2
|
UTSW |
13 |
11,787,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R0285:Ryr2
|
UTSW |
13 |
11,731,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R0365:Ryr2
|
UTSW |
13 |
11,683,725 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0401:Ryr2
|
UTSW |
13 |
11,720,570 (GRCm39) |
missense |
probably benign |
0.45 |
R0415:Ryr2
|
UTSW |
13 |
11,884,042 (GRCm39) |
missense |
probably damaging |
0.97 |
R0418:Ryr2
|
UTSW |
13 |
11,848,981 (GRCm39) |
splice site |
probably benign |
|
R0558:Ryr2
|
UTSW |
13 |
11,814,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R0558:Ryr2
|
UTSW |
13 |
11,653,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R0574:Ryr2
|
UTSW |
13 |
11,746,555 (GRCm39) |
missense |
probably benign |
0.02 |
R0586:Ryr2
|
UTSW |
13 |
11,650,445 (GRCm39) |
missense |
probably null |
|
R0601:Ryr2
|
UTSW |
13 |
11,720,519 (GRCm39) |
critical splice donor site |
probably null |
|
R0610:Ryr2
|
UTSW |
13 |
11,637,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R0648:Ryr2
|
UTSW |
13 |
11,739,219 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0727:Ryr2
|
UTSW |
13 |
11,581,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R0743:Ryr2
|
UTSW |
13 |
11,569,415 (GRCm39) |
missense |
probably damaging |
0.99 |
R0821:Ryr2
|
UTSW |
13 |
11,753,012 (GRCm39) |
missense |
probably benign |
0.35 |
R0884:Ryr2
|
UTSW |
13 |
11,569,415 (GRCm39) |
missense |
probably damaging |
0.99 |
R1104:Ryr2
|
UTSW |
13 |
11,684,855 (GRCm39) |
missense |
probably damaging |
0.99 |
R1114:Ryr2
|
UTSW |
13 |
11,960,867 (GRCm39) |
missense |
probably damaging |
0.98 |
R1167:Ryr2
|
UTSW |
13 |
11,674,999 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1238:Ryr2
|
UTSW |
13 |
11,774,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R1239:Ryr2
|
UTSW |
13 |
11,897,929 (GRCm39) |
critical splice donor site |
probably null |
|
R1296:Ryr2
|
UTSW |
13 |
11,702,765 (GRCm39) |
splice site |
probably benign |
|
R1400:Ryr2
|
UTSW |
13 |
11,609,962 (GRCm39) |
missense |
probably benign |
0.08 |
R1439:Ryr2
|
UTSW |
13 |
11,729,389 (GRCm39) |
splice site |
probably benign |
|
R1443:Ryr2
|
UTSW |
13 |
11,794,152 (GRCm39) |
missense |
probably benign |
0.19 |
R1446:Ryr2
|
UTSW |
13 |
11,753,035 (GRCm39) |
missense |
probably benign |
0.09 |
R1458:Ryr2
|
UTSW |
13 |
11,741,908 (GRCm39) |
missense |
probably damaging |
0.97 |
R1497:Ryr2
|
UTSW |
13 |
11,616,727 (GRCm39) |
missense |
probably damaging |
0.99 |
R1505:Ryr2
|
UTSW |
13 |
11,569,478 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1548:Ryr2
|
UTSW |
13 |
11,569,435 (GRCm39) |
nonsense |
probably null |
|
R1551:Ryr2
|
UTSW |
13 |
11,800,029 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1567:Ryr2
|
UTSW |
13 |
11,774,563 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1581:Ryr2
|
UTSW |
13 |
11,809,449 (GRCm39) |
missense |
probably benign |
0.01 |
R1645:Ryr2
|
UTSW |
13 |
11,733,368 (GRCm39) |
nonsense |
probably null |
|
R1686:Ryr2
|
UTSW |
13 |
11,618,665 (GRCm39) |
splice site |
probably benign |
|
R1696:Ryr2
|
UTSW |
13 |
11,746,543 (GRCm39) |
missense |
probably benign |
0.02 |
R1708:Ryr2
|
UTSW |
13 |
11,602,328 (GRCm39) |
splice site |
probably null |
|
R1745:Ryr2
|
UTSW |
13 |
11,805,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R1771:Ryr2
|
UTSW |
13 |
11,760,062 (GRCm39) |
critical splice donor site |
probably null |
|
R1776:Ryr2
|
UTSW |
13 |
11,760,062 (GRCm39) |
critical splice donor site |
probably null |
|
R1783:Ryr2
|
UTSW |
13 |
11,715,257 (GRCm39) |
nonsense |
probably null |
|
R1801:Ryr2
|
UTSW |
13 |
11,610,167 (GRCm39) |
missense |
probably benign |
0.01 |
R1812:Ryr2
|
UTSW |
13 |
11,575,472 (GRCm39) |
missense |
probably damaging |
0.97 |
R1820:Ryr2
|
UTSW |
13 |
11,602,202 (GRCm39) |
missense |
probably damaging |
0.99 |
R1835:Ryr2
|
UTSW |
13 |
11,784,764 (GRCm39) |
missense |
probably benign |
0.06 |
R1868:Ryr2
|
UTSW |
13 |
11,746,586 (GRCm39) |
missense |
probably benign |
0.02 |
R1869:Ryr2
|
UTSW |
13 |
11,676,961 (GRCm39) |
missense |
probably damaging |
0.98 |
R1884:Ryr2
|
UTSW |
13 |
11,753,242 (GRCm39) |
missense |
probably damaging |
0.97 |
R1892:Ryr2
|
UTSW |
13 |
11,673,844 (GRCm39) |
nonsense |
probably null |
|
R1897:Ryr2
|
UTSW |
13 |
11,765,818 (GRCm39) |
missense |
probably benign |
0.09 |
R1899:Ryr2
|
UTSW |
13 |
11,606,222 (GRCm39) |
missense |
probably benign |
|
R1909:Ryr2
|
UTSW |
13 |
11,715,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R1918:Ryr2
|
UTSW |
13 |
11,571,584 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1937:Ryr2
|
UTSW |
13 |
11,683,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R1943:Ryr2
|
UTSW |
13 |
11,746,609 (GRCm39) |
missense |
probably benign |
0.10 |
R1956:Ryr2
|
UTSW |
13 |
11,695,966 (GRCm39) |
missense |
probably damaging |
1.00 |
R1983:Ryr2
|
UTSW |
13 |
11,600,288 (GRCm39) |
splice site |
probably null |
|
R2018:Ryr2
|
UTSW |
13 |
11,866,074 (GRCm39) |
missense |
possibly damaging |
0.59 |
R2019:Ryr2
|
UTSW |
13 |
11,866,074 (GRCm39) |
missense |
possibly damaging |
0.59 |
R2060:Ryr2
|
UTSW |
13 |
11,610,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R2061:Ryr2
|
UTSW |
13 |
11,680,764 (GRCm39) |
splice site |
probably null |
|
R2088:Ryr2
|
UTSW |
13 |
11,677,115 (GRCm39) |
missense |
probably benign |
0.04 |
R2089:Ryr2
|
UTSW |
13 |
11,960,863 (GRCm39) |
missense |
probably benign |
0.23 |
R2091:Ryr2
|
UTSW |
13 |
11,960,863 (GRCm39) |
missense |
probably benign |
0.23 |
R2091:Ryr2
|
UTSW |
13 |
11,960,863 (GRCm39) |
missense |
probably benign |
0.23 |
R2127:Ryr2
|
UTSW |
13 |
11,727,081 (GRCm39) |
missense |
probably damaging |
1.00 |
R2140:Ryr2
|
UTSW |
13 |
11,575,493 (GRCm39) |
missense |
probably damaging |
1.00 |
R2153:Ryr2
|
UTSW |
13 |
11,592,759 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2179:Ryr2
|
UTSW |
13 |
11,720,679 (GRCm39) |
nonsense |
probably null |
|
R2207:Ryr2
|
UTSW |
13 |
11,825,823 (GRCm39) |
missense |
probably damaging |
1.00 |
R2237:Ryr2
|
UTSW |
13 |
11,677,146 (GRCm39) |
missense |
probably benign |
0.18 |
R2258:Ryr2
|
UTSW |
13 |
11,753,102 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2312:Ryr2
|
UTSW |
13 |
11,753,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R2421:Ryr2
|
UTSW |
13 |
11,606,123 (GRCm39) |
missense |
probably damaging |
0.98 |
R2438:Ryr2
|
UTSW |
13 |
11,816,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R2483:Ryr2
|
UTSW |
13 |
11,774,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R2860:Ryr2
|
UTSW |
13 |
11,607,979 (GRCm39) |
missense |
probably damaging |
0.98 |
R2861:Ryr2
|
UTSW |
13 |
11,607,979 (GRCm39) |
missense |
probably damaging |
0.98 |
R2867:Ryr2
|
UTSW |
13 |
11,776,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R2867:Ryr2
|
UTSW |
13 |
11,776,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R3618:Ryr2
|
UTSW |
13 |
11,787,466 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3876:Ryr2
|
UTSW |
13 |
11,603,045 (GRCm39) |
missense |
probably damaging |
0.99 |
R3906:Ryr2
|
UTSW |
13 |
11,753,095 (GRCm39) |
missense |
possibly damaging |
0.87 |
R3912:Ryr2
|
UTSW |
13 |
11,787,313 (GRCm39) |
missense |
probably damaging |
0.99 |
R4018:Ryr2
|
UTSW |
13 |
11,933,300 (GRCm39) |
missense |
probably damaging |
1.00 |
R4114:Ryr2
|
UTSW |
13 |
11,707,568 (GRCm39) |
missense |
probably damaging |
1.00 |
R4119:Ryr2
|
UTSW |
13 |
11,794,153 (GRCm39) |
missense |
probably benign |
0.22 |
R4127:Ryr2
|
UTSW |
13 |
11,602,323 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4222:Ryr2
|
UTSW |
13 |
11,752,759 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4233:Ryr2
|
UTSW |
13 |
11,765,611 (GRCm39) |
missense |
probably benign |
0.20 |
R4355:Ryr2
|
UTSW |
13 |
11,664,698 (GRCm39) |
missense |
probably benign |
0.05 |
R4384:Ryr2
|
UTSW |
13 |
11,620,119 (GRCm39) |
missense |
probably damaging |
0.99 |
R4422:Ryr2
|
UTSW |
13 |
11,731,952 (GRCm39) |
nonsense |
probably null |
|
R4430:Ryr2
|
UTSW |
13 |
11,750,413 (GRCm39) |
missense |
probably damaging |
0.98 |
R4624:Ryr2
|
UTSW |
13 |
12,121,301 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4663:Ryr2
|
UTSW |
13 |
11,764,395 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4665:Ryr2
|
UTSW |
13 |
11,765,571 (GRCm39) |
splice site |
probably null |
|
R4668:Ryr2
|
UTSW |
13 |
11,608,003 (GRCm39) |
missense |
probably benign |
|
R4677:Ryr2
|
UTSW |
13 |
11,721,553 (GRCm39) |
missense |
probably damaging |
0.98 |
R4679:Ryr2
|
UTSW |
13 |
11,839,255 (GRCm39) |
missense |
probably benign |
0.34 |
R4680:Ryr2
|
UTSW |
13 |
11,610,119 (GRCm39) |
missense |
probably benign |
0.04 |
R4685:Ryr2
|
UTSW |
13 |
11,707,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R4709:Ryr2
|
UTSW |
13 |
11,731,884 (GRCm39) |
missense |
probably damaging |
1.00 |
R4731:Ryr2
|
UTSW |
13 |
11,592,795 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4732:Ryr2
|
UTSW |
13 |
11,592,795 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4733:Ryr2
|
UTSW |
13 |
11,592,795 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4734:Ryr2
|
UTSW |
13 |
11,752,639 (GRCm39) |
missense |
probably damaging |
0.99 |
R4740:Ryr2
|
UTSW |
13 |
11,671,933 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4801:Ryr2
|
UTSW |
13 |
11,702,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R4801:Ryr2
|
UTSW |
13 |
11,723,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R4802:Ryr2
|
UTSW |
13 |
11,702,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R4802:Ryr2
|
UTSW |
13 |
11,723,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R4804:Ryr2
|
UTSW |
13 |
11,731,983 (GRCm39) |
missense |
probably damaging |
1.00 |
R4811:Ryr2
|
UTSW |
13 |
11,670,584 (GRCm39) |
missense |
probably damaging |
0.97 |
R4850:Ryr2
|
UTSW |
13 |
11,760,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R4850:Ryr2
|
UTSW |
13 |
11,683,706 (GRCm39) |
missense |
probably damaging |
0.99 |
R4880:Ryr2
|
UTSW |
13 |
11,767,104 (GRCm39) |
missense |
probably damaging |
1.00 |
R4917:Ryr2
|
UTSW |
13 |
11,609,872 (GRCm39) |
missense |
probably damaging |
0.96 |
R4918:Ryr2
|
UTSW |
13 |
11,609,872 (GRCm39) |
missense |
probably damaging |
0.96 |
R4922:Ryr2
|
UTSW |
13 |
11,724,849 (GRCm39) |
missense |
probably damaging |
0.99 |
R4933:Ryr2
|
UTSW |
13 |
11,960,831 (GRCm39) |
missense |
probably damaging |
0.96 |
R4950:Ryr2
|
UTSW |
13 |
11,756,897 (GRCm39) |
missense |
probably damaging |
1.00 |
R4957:Ryr2
|
UTSW |
13 |
11,799,966 (GRCm39) |
missense |
probably damaging |
0.97 |
R4964:Ryr2
|
UTSW |
13 |
11,848,878 (GRCm39) |
missense |
probably benign |
0.00 |
R4964:Ryr2
|
UTSW |
13 |
11,729,497 (GRCm39) |
missense |
possibly damaging |
0.49 |
R4966:Ryr2
|
UTSW |
13 |
11,729,497 (GRCm39) |
missense |
possibly damaging |
0.49 |
R4966:Ryr2
|
UTSW |
13 |
11,848,878 (GRCm39) |
missense |
probably benign |
0.00 |
R4997:Ryr2
|
UTSW |
13 |
11,610,192 (GRCm39) |
missense |
probably benign |
0.09 |
R4998:Ryr2
|
UTSW |
13 |
11,658,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R5033:Ryr2
|
UTSW |
13 |
11,602,140 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5061:Ryr2
|
UTSW |
13 |
11,650,422 (GRCm39) |
missense |
possibly damaging |
0.74 |
R5062:Ryr2
|
UTSW |
13 |
11,715,240 (GRCm39) |
missense |
probably damaging |
0.97 |
R5088:Ryr2
|
UTSW |
13 |
11,727,129 (GRCm39) |
nonsense |
probably null |
|
R5135:Ryr2
|
UTSW |
13 |
11,677,016 (GRCm39) |
missense |
probably benign |
0.05 |
R5138:Ryr2
|
UTSW |
13 |
11,675,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R5168:Ryr2
|
UTSW |
13 |
11,767,207 (GRCm39) |
missense |
probably benign |
|
R5187:Ryr2
|
UTSW |
13 |
11,787,338 (GRCm39) |
missense |
probably damaging |
0.99 |
R5197:Ryr2
|
UTSW |
13 |
11,653,316 (GRCm39) |
critical splice donor site |
probably null |
|
R5262:Ryr2
|
UTSW |
13 |
11,787,323 (GRCm39) |
missense |
probably damaging |
0.99 |
R5325:Ryr2
|
UTSW |
13 |
11,705,249 (GRCm39) |
missense |
probably damaging |
0.97 |
R5381:Ryr2
|
UTSW |
13 |
11,571,544 (GRCm39) |
missense |
probably damaging |
1.00 |
R5437:Ryr2
|
UTSW |
13 |
11,670,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R5477:Ryr2
|
UTSW |
13 |
11,720,542 (GRCm39) |
missense |
probably damaging |
1.00 |
R5497:Ryr2
|
UTSW |
13 |
11,720,587 (GRCm39) |
missense |
probably null |
0.15 |
R5509:Ryr2
|
UTSW |
13 |
11,760,487 (GRCm39) |
missense |
probably damaging |
0.98 |
R5518:Ryr2
|
UTSW |
13 |
11,702,795 (GRCm39) |
missense |
probably benign |
0.01 |
R5571:Ryr2
|
UTSW |
13 |
11,570,334 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5591:Ryr2
|
UTSW |
13 |
11,609,900 (GRCm39) |
missense |
probably benign |
0.06 |
R5619:Ryr2
|
UTSW |
13 |
11,723,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R5630:Ryr2
|
UTSW |
13 |
11,616,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R5644:Ryr2
|
UTSW |
13 |
11,610,468 (GRCm39) |
missense |
probably damaging |
0.99 |
R5667:Ryr2
|
UTSW |
13 |
11,774,722 (GRCm39) |
missense |
probably damaging |
1.00 |
R5775:Ryr2
|
UTSW |
13 |
11,784,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R5836:Ryr2
|
UTSW |
13 |
11,618,618 (GRCm39) |
missense |
probably damaging |
1.00 |
R5858:Ryr2
|
UTSW |
13 |
11,575,460 (GRCm39) |
missense |
probably damaging |
0.99 |
R5934:Ryr2
|
UTSW |
13 |
11,599,040 (GRCm39) |
missense |
probably damaging |
0.96 |
R5939:Ryr2
|
UTSW |
13 |
11,805,218 (GRCm39) |
missense |
probably damaging |
0.99 |
R5941:Ryr2
|
UTSW |
13 |
11,702,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R5945:Ryr2
|
UTSW |
13 |
11,675,008 (GRCm39) |
missense |
probably damaging |
1.00 |
R5946:Ryr2
|
UTSW |
13 |
11,741,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R5966:Ryr2
|
UTSW |
13 |
11,677,124 (GRCm39) |
nonsense |
probably null |
|
R5974:Ryr2
|
UTSW |
13 |
11,729,397 (GRCm39) |
splice site |
probably null |
|
R6104:Ryr2
|
UTSW |
13 |
11,814,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R6118:Ryr2
|
UTSW |
13 |
11,807,575 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6149:Ryr2
|
UTSW |
13 |
11,683,903 (GRCm39) |
missense |
probably benign |
|
R6208:Ryr2
|
UTSW |
13 |
11,910,106 (GRCm39) |
missense |
probably benign |
0.04 |
R6217:Ryr2
|
UTSW |
13 |
11,848,964 (GRCm39) |
missense |
probably damaging |
1.00 |
R6230:Ryr2
|
UTSW |
13 |
11,674,993 (GRCm39) |
missense |
probably damaging |
0.99 |
R6279:Ryr2
|
UTSW |
13 |
11,695,885 (GRCm39) |
missense |
probably damaging |
0.97 |
R6294:Ryr2
|
UTSW |
13 |
11,894,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R6300:Ryr2
|
UTSW |
13 |
11,695,885 (GRCm39) |
missense |
probably damaging |
0.97 |
R6350:Ryr2
|
UTSW |
13 |
11,776,282 (GRCm39) |
missense |
probably damaging |
0.98 |
R6484:Ryr2
|
UTSW |
13 |
11,677,269 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6489:Ryr2
|
UTSW |
13 |
11,848,893 (GRCm39) |
missense |
probably benign |
0.29 |
R6548:Ryr2
|
UTSW |
13 |
11,683,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R6591:Ryr2
|
UTSW |
13 |
11,609,609 (GRCm39) |
missense |
probably benign |
0.01 |
R6623:Ryr2
|
UTSW |
13 |
11,724,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R6649:Ryr2
|
UTSW |
13 |
11,610,529 (GRCm39) |
missense |
probably damaging |
0.99 |
R6691:Ryr2
|
UTSW |
13 |
11,609,609 (GRCm39) |
missense |
probably benign |
0.01 |
R6770:Ryr2
|
UTSW |
13 |
11,753,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R6802:Ryr2
|
UTSW |
13 |
11,701,852 (GRCm39) |
missense |
probably damaging |
1.00 |
R6809:Ryr2
|
UTSW |
13 |
11,741,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R6893:Ryr2
|
UTSW |
13 |
11,844,540 (GRCm39) |
missense |
possibly damaging |
0.75 |
R6911:Ryr2
|
UTSW |
13 |
11,842,445 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6915:Ryr2
|
UTSW |
13 |
11,760,487 (GRCm39) |
missense |
probably damaging |
1.00 |
R6943:Ryr2
|
UTSW |
13 |
11,581,834 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6960:Ryr2
|
UTSW |
13 |
11,816,129 (GRCm39) |
missense |
probably benign |
0.28 |
R6997:Ryr2
|
UTSW |
13 |
11,669,266 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6998:Ryr2
|
UTSW |
13 |
11,727,052 (GRCm39) |
missense |
probably damaging |
0.99 |
R7001:Ryr2
|
UTSW |
13 |
11,809,491 (GRCm39) |
missense |
probably damaging |
0.98 |
R7047:Ryr2
|
UTSW |
13 |
11,839,286 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7089:Ryr2
|
UTSW |
13 |
11,664,662 (GRCm39) |
missense |
probably benign |
0.10 |
R7125:Ryr2
|
UTSW |
13 |
11,684,873 (GRCm39) |
missense |
probably damaging |
0.99 |
R7127:Ryr2
|
UTSW |
13 |
11,670,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R7131:Ryr2
|
UTSW |
13 |
11,683,697 (GRCm39) |
critical splice donor site |
probably null |
|
R7131:Ryr2
|
UTSW |
13 |
11,655,213 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7159:Ryr2
|
UTSW |
13 |
11,825,794 (GRCm39) |
missense |
probably damaging |
0.99 |
R7174:Ryr2
|
UTSW |
13 |
11,816,063 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7180:Ryr2
|
UTSW |
13 |
11,701,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R7182:Ryr2
|
UTSW |
13 |
11,774,643 (GRCm39) |
missense |
probably benign |
|
R7189:Ryr2
|
UTSW |
13 |
11,898,009 (GRCm39) |
missense |
probably damaging |
1.00 |
R7241:Ryr2
|
UTSW |
13 |
11,680,799 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7244:Ryr2
|
UTSW |
13 |
11,612,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R7326:Ryr2
|
UTSW |
13 |
11,753,080 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7331:Ryr2
|
UTSW |
13 |
11,760,517 (GRCm39) |
missense |
probably benign |
|
R7365:Ryr2
|
UTSW |
13 |
11,655,161 (GRCm39) |
missense |
probably damaging |
0.99 |
R7372:Ryr2
|
UTSW |
13 |
11,695,885 (GRCm39) |
missense |
probably damaging |
0.97 |
R7395:Ryr2
|
UTSW |
13 |
11,799,997 (GRCm39) |
missense |
probably damaging |
0.98 |
R7404:Ryr2
|
UTSW |
13 |
11,750,506 (GRCm39) |
missense |
probably damaging |
0.97 |
R7417:Ryr2
|
UTSW |
13 |
11,571,634 (GRCm39) |
splice site |
probably null |
|
R7425:Ryr2
|
UTSW |
13 |
11,720,530 (GRCm39) |
missense |
probably benign |
0.20 |
R7444:Ryr2
|
UTSW |
13 |
11,570,349 (GRCm39) |
missense |
probably benign |
0.25 |
R7456:Ryr2
|
UTSW |
13 |
11,767,168 (GRCm39) |
missense |
probably benign |
|
R7460:Ryr2
|
UTSW |
13 |
11,720,596 (GRCm39) |
missense |
probably benign |
0.10 |
R7474:Ryr2
|
UTSW |
13 |
11,609,762 (GRCm39) |
missense |
probably benign |
0.04 |
R7543:Ryr2
|
UTSW |
13 |
11,653,317 (GRCm39) |
critical splice donor site |
probably null |
|
R7549:Ryr2
|
UTSW |
13 |
11,752,871 (GRCm39) |
missense |
probably benign |
0.15 |
R7558:Ryr2
|
UTSW |
13 |
11,814,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R7565:Ryr2
|
UTSW |
13 |
11,575,539 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7627:Ryr2
|
UTSW |
13 |
11,776,213 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7698:Ryr2
|
UTSW |
13 |
11,776,201 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7702:Ryr2
|
UTSW |
13 |
11,705,219 (GRCm39) |
missense |
probably damaging |
0.99 |
R7719:Ryr2
|
UTSW |
13 |
11,745,229 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7772:Ryr2
|
UTSW |
13 |
11,765,897 (GRCm39) |
missense |
probably benign |
|
R7797:Ryr2
|
UTSW |
13 |
11,816,066 (GRCm39) |
missense |
probably damaging |
0.99 |
R7829:Ryr2
|
UTSW |
13 |
11,842,493 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7855:Ryr2
|
UTSW |
13 |
11,721,509 (GRCm39) |
nonsense |
probably null |
|
R7872:Ryr2
|
UTSW |
13 |
11,610,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R7908:Ryr2
|
UTSW |
13 |
11,807,634 (GRCm39) |
missense |
probably benign |
0.01 |
R7929:Ryr2
|
UTSW |
13 |
11,609,680 (GRCm39) |
missense |
probably damaging |
1.00 |
R7929:Ryr2
|
UTSW |
13 |
11,705,181 (GRCm39) |
nonsense |
probably null |
|
R7952:Ryr2
|
UTSW |
13 |
11,661,313 (GRCm39) |
splice site |
probably null |
|
R8008:Ryr2
|
UTSW |
13 |
11,671,980 (GRCm39) |
missense |
probably benign |
0.30 |
R8011:Ryr2
|
UTSW |
13 |
11,603,026 (GRCm39) |
critical splice donor site |
probably null |
|
R8097:Ryr2
|
UTSW |
13 |
11,960,881 (GRCm39) |
missense |
probably damaging |
0.98 |
R8133:Ryr2
|
UTSW |
13 |
11,618,584 (GRCm39) |
missense |
probably damaging |
1.00 |
R8253:Ryr2
|
UTSW |
13 |
11,842,439 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8278:Ryr2
|
UTSW |
13 |
11,610,392 (GRCm39) |
nonsense |
probably null |
|
R8351:Ryr2
|
UTSW |
13 |
11,814,718 (GRCm39) |
missense |
probably damaging |
0.98 |
R8401:Ryr2
|
UTSW |
13 |
11,683,821 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8403:Ryr2
|
UTSW |
13 |
11,699,364 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8431:Ryr2
|
UTSW |
13 |
11,673,894 (GRCm39) |
missense |
probably benign |
0.00 |
R8509:Ryr2
|
UTSW |
13 |
11,592,664 (GRCm39) |
critical splice donor site |
probably null |
|
R8551:Ryr2
|
UTSW |
13 |
11,575,479 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8684:Ryr2
|
UTSW |
13 |
11,702,875 (GRCm39) |
missense |
probably damaging |
0.99 |
R8735:Ryr2
|
UTSW |
13 |
11,701,833 (GRCm39) |
missense |
probably damaging |
0.97 |
R8766:Ryr2
|
UTSW |
13 |
11,683,855 (GRCm39) |
missense |
probably damaging |
0.97 |
R8817:Ryr2
|
UTSW |
13 |
11,750,509 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8827:Ryr2
|
UTSW |
13 |
11,572,934 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8884:Ryr2
|
UTSW |
13 |
11,794,152 (GRCm39) |
missense |
probably benign |
0.19 |
R8889:Ryr2
|
UTSW |
13 |
11,799,990 (GRCm39) |
missense |
probably damaging |
0.99 |
R8891:Ryr2
|
UTSW |
13 |
11,814,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R8979:Ryr2
|
UTSW |
13 |
11,609,924 (GRCm39) |
missense |
probably benign |
0.00 |
R9013:Ryr2
|
UTSW |
13 |
11,618,618 (GRCm39) |
missense |
probably damaging |
0.98 |
R9040:Ryr2
|
UTSW |
13 |
11,609,672 (GRCm39) |
missense |
probably damaging |
0.97 |
R9044:Ryr2
|
UTSW |
13 |
11,752,989 (GRCm39) |
nonsense |
probably null |
|
R9056:Ryr2
|
UTSW |
13 |
11,610,817 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9084:Ryr2
|
UTSW |
13 |
11,616,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R9113:Ryr2
|
UTSW |
13 |
11,618,741 (GRCm39) |
intron |
probably benign |
|
R9116:Ryr2
|
UTSW |
13 |
11,587,185 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9125:Ryr2
|
UTSW |
13 |
11,669,292 (GRCm39) |
missense |
probably benign |
0.28 |
R9148:Ryr2
|
UTSW |
13 |
11,900,424 (GRCm39) |
missense |
probably benign |
0.02 |
R9210:Ryr2
|
UTSW |
13 |
11,844,560 (GRCm39) |
missense |
probably damaging |
0.99 |
R9212:Ryr2
|
UTSW |
13 |
11,844,560 (GRCm39) |
missense |
probably damaging |
0.99 |
R9233:Ryr2
|
UTSW |
13 |
11,610,772 (GRCm39) |
missense |
possibly damaging |
0.77 |
R9254:Ryr2
|
UTSW |
13 |
11,898,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R9262:Ryr2
|
UTSW |
13 |
11,765,854 (GRCm39) |
missense |
probably damaging |
0.97 |
R9275:Ryr2
|
UTSW |
13 |
11,897,976 (GRCm39) |
missense |
probably benign |
0.10 |
R9278:Ryr2
|
UTSW |
13 |
11,897,976 (GRCm39) |
missense |
probably benign |
0.10 |
R9309:Ryr2
|
UTSW |
13 |
11,721,578 (GRCm39) |
missense |
probably damaging |
0.99 |
R9379:Ryr2
|
UTSW |
13 |
11,898,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R9409:Ryr2
|
UTSW |
13 |
11,695,973 (GRCm39) |
missense |
probably damaging |
0.99 |
R9429:Ryr2
|
UTSW |
13 |
11,809,459 (GRCm39) |
missense |
probably damaging |
0.97 |
R9445:Ryr2
|
UTSW |
13 |
11,787,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R9464:Ryr2
|
UTSW |
13 |
11,752,680 (GRCm39) |
missense |
probably benign |
0.00 |
R9467:Ryr2
|
UTSW |
13 |
11,571,490 (GRCm39) |
missense |
possibly damaging |
0.70 |
R9546:Ryr2
|
UTSW |
13 |
11,602,101 (GRCm39) |
critical splice donor site |
probably null |
|
R9562:Ryr2
|
UTSW |
13 |
11,760,104 (GRCm39) |
missense |
probably damaging |
1.00 |
R9609:Ryr2
|
UTSW |
13 |
11,683,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R9704:Ryr2
|
UTSW |
13 |
11,737,646 (GRCm39) |
missense |
probably damaging |
1.00 |
R9764:Ryr2
|
UTSW |
13 |
11,701,935 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9772:Ryr2
|
UTSW |
13 |
11,609,785 (GRCm39) |
missense |
probably benign |
0.13 |
R9776:Ryr2
|
UTSW |
13 |
11,707,599 (GRCm39) |
missense |
probably damaging |
0.98 |
S24628:Ryr2
|
UTSW |
13 |
11,884,042 (GRCm39) |
missense |
probably damaging |
0.97 |
X0019:Ryr2
|
UTSW |
13 |
11,718,387 (GRCm39) |
missense |
probably benign |
0.04 |
Z1176:Ryr2
|
UTSW |
13 |
11,658,689 (GRCm39) |
critical splice donor site |
probably null |
|
Z1176:Ryr2
|
UTSW |
13 |
11,613,497 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1176:Ryr2
|
UTSW |
13 |
11,809,435 (GRCm39) |
nonsense |
probably null |
|
Z1177:Ryr2
|
UTSW |
13 |
11,765,759 (GRCm39) |
missense |
possibly damaging |
0.87 |
|