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 |
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: 135,899,865 (GRCm39) |
R482Q |
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: 136,396,017 (GRCm39) |
N108D |
probably benign |
Het |
Kif14 |
T |
C |
1: 136,453,521 (GRCm39) |
V1433A |
probably benign |
Het |
Kif14 |
T |
C |
1: 136,443,699 (GRCm39) |
F1291L |
probably benign |
Het |
Kif14 |
C |
T |
1: 136,431,169 (GRCm39) |
L1189F |
probably benign |
Het |
Kif14 |
A |
G |
1: 136,418,070 (GRCm39) |
S868G |
probably benign |
Het |
Kif14 |
G |
A |
1: 136,406,103 (GRCm39) |
A556T |
probably benign |
Het |
Kif14 |
A |
G |
1: 136,396,713 (GRCm39) |
K340E |
probably damaging |
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: 135,755,119 (GRCm39) |
P132S |
possibly damaging |
Het |
Lad1 |
C |
T |
1: 135,755,761 (GRCm39) |
R346C |
probably damaging |
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 |
Lax1 |
T |
C |
1: 133,608,307 (GRCm39) |
N145D |
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 |
Lgr6 |
C |
T |
1: 134,914,826 (GRCm39) |
V641I |
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 |
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 |
Ryr2 |
C |
T |
13: 11,602,308 (GRCm39) |
V4525M |
possibly damaging |
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 |
T |
C |
1: 120,155,480 (GRCm39) |
N493S |
probably benign |
Het |
Steap3 |
G |
A |
1: 120,162,108 (GRCm39) |
A350V |
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 Mycbp2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00094:Mycbp2
|
APN |
14 |
103,460,486 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00518:Mycbp2
|
APN |
14 |
103,393,244 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00650:Mycbp2
|
APN |
14 |
103,380,664 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL00653:Mycbp2
|
APN |
14 |
103,380,664 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL00742:Mycbp2
|
APN |
14 |
103,438,788 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00755:Mycbp2
|
APN |
14 |
103,432,057 (GRCm39) |
missense |
possibly damaging |
0.72 |
IGL00793:Mycbp2
|
APN |
14 |
103,364,189 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL00916:Mycbp2
|
APN |
14 |
103,528,719 (GRCm39) |
splice site |
probably benign |
|
IGL00960:Mycbp2
|
APN |
14 |
103,466,820 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL00977:Mycbp2
|
APN |
14 |
103,410,078 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01349:Mycbp2
|
APN |
14 |
103,359,983 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01369:Mycbp2
|
APN |
14 |
103,392,946 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL01410:Mycbp2
|
APN |
14 |
103,466,928 (GRCm39) |
splice site |
probably null |
|
IGL01586:Mycbp2
|
APN |
14 |
103,378,305 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01593:Mycbp2
|
APN |
14 |
103,528,723 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01693:Mycbp2
|
APN |
14 |
103,365,415 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01730:Mycbp2
|
APN |
14 |
103,372,640 (GRCm39) |
nonsense |
probably null |
|
IGL01820:Mycbp2
|
APN |
14 |
103,425,937 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01974:Mycbp2
|
APN |
14 |
103,380,647 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02071:Mycbp2
|
APN |
14 |
103,392,343 (GRCm39) |
nonsense |
probably null |
|
IGL02178:Mycbp2
|
APN |
14 |
103,461,802 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02324:Mycbp2
|
APN |
14 |
103,479,643 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02442:Mycbp2
|
APN |
14 |
103,551,811 (GRCm39) |
missense |
probably benign |
|
IGL02607:Mycbp2
|
APN |
14 |
103,522,709 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02679:Mycbp2
|
APN |
14 |
103,442,621 (GRCm39) |
missense |
probably benign |
|
IGL02702:Mycbp2
|
APN |
14 |
103,457,560 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02709:Mycbp2
|
APN |
14 |
103,392,697 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02736:Mycbp2
|
APN |
14 |
103,351,678 (GRCm39) |
splice site |
probably benign |
|
IGL02866:Mycbp2
|
APN |
14 |
103,367,428 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02939:Mycbp2
|
APN |
14 |
103,414,715 (GRCm39) |
missense |
probably benign |
|
IGL03082:Mycbp2
|
APN |
14 |
103,441,805 (GRCm39) |
missense |
probably benign |
0.23 |
IGL03142:Mycbp2
|
APN |
14 |
103,536,212 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03155:Mycbp2
|
APN |
14 |
103,392,889 (GRCm39) |
missense |
probably benign |
0.06 |
IGL03236:Mycbp2
|
APN |
14 |
103,536,134 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03256:Mycbp2
|
APN |
14 |
103,426,025 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL03303:Mycbp2
|
APN |
14 |
103,485,194 (GRCm39) |
missense |
probably damaging |
1.00 |
compost
|
UTSW |
14 |
103,393,889 (GRCm39) |
missense |
probably damaging |
1.00 |
decompose
|
UTSW |
14 |
103,457,415 (GRCm39) |
missense |
probably benign |
0.12 |
moulder
|
UTSW |
14 |
103,426,028 (GRCm39) |
missense |
probably damaging |
1.00 |
N/A - 293:Mycbp2
|
UTSW |
14 |
103,461,898 (GRCm39) |
splice site |
probably benign |
|
R0040:Mycbp2
|
UTSW |
14 |
103,461,708 (GRCm39) |
missense |
probably benign |
0.11 |
R0040:Mycbp2
|
UTSW |
14 |
103,461,708 (GRCm39) |
missense |
probably benign |
0.11 |
R0057:Mycbp2
|
UTSW |
14 |
103,389,578 (GRCm39) |
missense |
probably damaging |
0.97 |
R0063:Mycbp2
|
UTSW |
14 |
103,394,070 (GRCm39) |
unclassified |
probably benign |
|
R0097:Mycbp2
|
UTSW |
14 |
103,393,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R0097:Mycbp2
|
UTSW |
14 |
103,393,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R0268:Mycbp2
|
UTSW |
14 |
103,551,761 (GRCm39) |
nonsense |
probably null |
|
R0388:Mycbp2
|
UTSW |
14 |
103,394,103 (GRCm39) |
missense |
probably benign |
0.01 |
R0410:Mycbp2
|
UTSW |
14 |
103,372,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R0530:Mycbp2
|
UTSW |
14 |
103,419,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R0591:Mycbp2
|
UTSW |
14 |
103,433,827 (GRCm39) |
unclassified |
probably benign |
|
R0671:Mycbp2
|
UTSW |
14 |
103,432,024 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0755:Mycbp2
|
UTSW |
14 |
103,412,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R0817:Mycbp2
|
UTSW |
14 |
103,466,854 (GRCm39) |
missense |
probably damaging |
0.99 |
R0818:Mycbp2
|
UTSW |
14 |
103,466,854 (GRCm39) |
missense |
probably damaging |
0.99 |
R0819:Mycbp2
|
UTSW |
14 |
103,466,854 (GRCm39) |
missense |
probably damaging |
0.99 |
R0881:Mycbp2
|
UTSW |
14 |
103,457,449 (GRCm39) |
missense |
probably benign |
|
R0903:Mycbp2
|
UTSW |
14 |
103,513,293 (GRCm39) |
missense |
probably damaging |
0.99 |
R0940:Mycbp2
|
UTSW |
14 |
103,500,129 (GRCm39) |
unclassified |
probably benign |
|
R0961:Mycbp2
|
UTSW |
14 |
103,422,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R1004:Mycbp2
|
UTSW |
14 |
103,378,353 (GRCm39) |
missense |
probably benign |
0.00 |
R1138:Mycbp2
|
UTSW |
14 |
103,412,262 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1170:Mycbp2
|
UTSW |
14 |
103,437,588 (GRCm39) |
nonsense |
probably null |
|
R1211:Mycbp2
|
UTSW |
14 |
103,357,999 (GRCm39) |
missense |
probably benign |
0.31 |
R1268:Mycbp2
|
UTSW |
14 |
103,446,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R1298:Mycbp2
|
UTSW |
14 |
103,393,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R1341:Mycbp2
|
UTSW |
14 |
103,536,303 (GRCm39) |
splice site |
probably benign |
|
R1469:Mycbp2
|
UTSW |
14 |
103,425,956 (GRCm39) |
missense |
probably damaging |
0.99 |
R1469:Mycbp2
|
UTSW |
14 |
103,425,956 (GRCm39) |
missense |
probably damaging |
0.99 |
R1513:Mycbp2
|
UTSW |
14 |
103,441,825 (GRCm39) |
missense |
probably damaging |
1.00 |
R1528:Mycbp2
|
UTSW |
14 |
103,470,033 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1564:Mycbp2
|
UTSW |
14 |
103,407,287 (GRCm39) |
splice site |
probably null |
|
R1565:Mycbp2
|
UTSW |
14 |
103,489,945 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1656:Mycbp2
|
UTSW |
14 |
103,485,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R1694:Mycbp2
|
UTSW |
14 |
103,464,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R1709:Mycbp2
|
UTSW |
14 |
103,461,852 (GRCm39) |
missense |
probably damaging |
1.00 |
R1751:Mycbp2
|
UTSW |
14 |
103,485,841 (GRCm39) |
missense |
probably damaging |
0.98 |
R1767:Mycbp2
|
UTSW |
14 |
103,485,841 (GRCm39) |
missense |
probably damaging |
0.98 |
R1772:Mycbp2
|
UTSW |
14 |
103,419,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R1784:Mycbp2
|
UTSW |
14 |
103,392,614 (GRCm39) |
missense |
probably damaging |
0.98 |
R1823:Mycbp2
|
UTSW |
14 |
103,489,945 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1824:Mycbp2
|
UTSW |
14 |
103,489,945 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1844:Mycbp2
|
UTSW |
14 |
103,393,150 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1916:Mycbp2
|
UTSW |
14 |
103,422,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R1944:Mycbp2
|
UTSW |
14 |
103,466,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R1983:Mycbp2
|
UTSW |
14 |
103,383,407 (GRCm39) |
missense |
probably damaging |
0.97 |
R2002:Mycbp2
|
UTSW |
14 |
103,485,839 (GRCm39) |
missense |
probably damaging |
0.98 |
R2031:Mycbp2
|
UTSW |
14 |
103,426,028 (GRCm39) |
missense |
probably damaging |
1.00 |
R2035:Mycbp2
|
UTSW |
14 |
103,497,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R2048:Mycbp2
|
UTSW |
14 |
103,469,960 (GRCm39) |
critical splice donor site |
probably null |
|
R2061:Mycbp2
|
UTSW |
14 |
103,524,696 (GRCm39) |
missense |
probably damaging |
0.99 |
R2113:Mycbp2
|
UTSW |
14 |
103,457,512 (GRCm39) |
missense |
probably damaging |
0.99 |
R2128:Mycbp2
|
UTSW |
14 |
103,438,666 (GRCm39) |
missense |
probably benign |
0.01 |
R2134:Mycbp2
|
UTSW |
14 |
103,446,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R2135:Mycbp2
|
UTSW |
14 |
103,446,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R2135:Mycbp2
|
UTSW |
14 |
103,383,378 (GRCm39) |
missense |
probably benign |
|
R2146:Mycbp2
|
UTSW |
14 |
103,393,358 (GRCm39) |
missense |
probably damaging |
0.97 |
R2147:Mycbp2
|
UTSW |
14 |
103,393,358 (GRCm39) |
missense |
probably damaging |
0.97 |
R2148:Mycbp2
|
UTSW |
14 |
103,393,358 (GRCm39) |
missense |
probably damaging |
0.97 |
R2150:Mycbp2
|
UTSW |
14 |
103,393,358 (GRCm39) |
missense |
probably damaging |
0.97 |
R2163:Mycbp2
|
UTSW |
14 |
103,407,291 (GRCm39) |
critical splice donor site |
probably null |
|
R2248:Mycbp2
|
UTSW |
14 |
103,407,295 (GRCm39) |
missense |
possibly damaging |
0.50 |
R2265:Mycbp2
|
UTSW |
14 |
103,500,185 (GRCm39) |
missense |
probably benign |
0.39 |
R2272:Mycbp2
|
UTSW |
14 |
103,381,774 (GRCm39) |
missense |
probably null |
0.66 |
R2379:Mycbp2
|
UTSW |
14 |
103,412,386 (GRCm39) |
missense |
probably benign |
|
R2495:Mycbp2
|
UTSW |
14 |
103,437,554 (GRCm39) |
missense |
probably damaging |
0.99 |
R2508:Mycbp2
|
UTSW |
14 |
103,368,681 (GRCm39) |
missense |
probably damaging |
0.99 |
R2510:Mycbp2
|
UTSW |
14 |
103,392,691 (GRCm39) |
missense |
probably damaging |
0.96 |
R2851:Mycbp2
|
UTSW |
14 |
103,381,769 (GRCm39) |
missense |
probably damaging |
0.99 |
R2852:Mycbp2
|
UTSW |
14 |
103,381,769 (GRCm39) |
missense |
probably damaging |
0.99 |
R2965:Mycbp2
|
UTSW |
14 |
103,534,794 (GRCm39) |
missense |
probably benign |
0.00 |
R3156:Mycbp2
|
UTSW |
14 |
103,446,179 (GRCm39) |
splice site |
probably benign |
|
R3404:Mycbp2
|
UTSW |
14 |
103,437,550 (GRCm39) |
missense |
probably damaging |
0.99 |
R3410:Mycbp2
|
UTSW |
14 |
103,372,553 (GRCm39) |
missense |
probably damaging |
1.00 |
R3429:Mycbp2
|
UTSW |
14 |
103,466,866 (GRCm39) |
missense |
probably damaging |
1.00 |
R3706:Mycbp2
|
UTSW |
14 |
103,393,850 (GRCm39) |
missense |
probably benign |
0.31 |
R3772:Mycbp2
|
UTSW |
14 |
103,371,224 (GRCm39) |
missense |
possibly damaging |
0.82 |
R3778:Mycbp2
|
UTSW |
14 |
103,434,721 (GRCm39) |
missense |
probably damaging |
0.99 |
R3883:Mycbp2
|
UTSW |
14 |
103,532,686 (GRCm39) |
missense |
probably damaging |
0.97 |
R3884:Mycbp2
|
UTSW |
14 |
103,532,686 (GRCm39) |
missense |
probably damaging |
0.97 |
R3887:Mycbp2
|
UTSW |
14 |
103,412,233 (GRCm39) |
missense |
probably damaging |
0.98 |
R3923:Mycbp2
|
UTSW |
14 |
103,364,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R3926:Mycbp2
|
UTSW |
14 |
103,441,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R3959:Mycbp2
|
UTSW |
14 |
103,532,688 (GRCm39) |
missense |
probably benign |
0.00 |
R3966:Mycbp2
|
UTSW |
14 |
103,376,161 (GRCm39) |
splice site |
probably benign |
|
R4021:Mycbp2
|
UTSW |
14 |
103,389,593 (GRCm39) |
missense |
probably damaging |
0.97 |
R4363:Mycbp2
|
UTSW |
14 |
103,485,893 (GRCm39) |
missense |
probably damaging |
1.00 |
R4405:Mycbp2
|
UTSW |
14 |
103,360,881 (GRCm39) |
missense |
probably damaging |
1.00 |
R4407:Mycbp2
|
UTSW |
14 |
103,524,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R4410:Mycbp2
|
UTSW |
14 |
103,372,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R4434:Mycbp2
|
UTSW |
14 |
103,371,225 (GRCm39) |
missense |
probably damaging |
0.99 |
R4448:Mycbp2
|
UTSW |
14 |
103,425,938 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4452:Mycbp2
|
UTSW |
14 |
103,393,094 (GRCm39) |
missense |
probably damaging |
0.99 |
R4573:Mycbp2
|
UTSW |
14 |
103,583,733 (GRCm39) |
missense |
probably benign |
0.05 |
R4589:Mycbp2
|
UTSW |
14 |
103,414,749 (GRCm39) |
missense |
probably benign |
0.04 |
R4621:Mycbp2
|
UTSW |
14 |
103,457,415 (GRCm39) |
missense |
probably benign |
0.12 |
R4622:Mycbp2
|
UTSW |
14 |
103,457,415 (GRCm39) |
missense |
probably benign |
0.12 |
R4729:Mycbp2
|
UTSW |
14 |
103,426,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R4770:Mycbp2
|
UTSW |
14 |
103,457,380 (GRCm39) |
missense |
probably benign |
0.41 |
R4790:Mycbp2
|
UTSW |
14 |
103,466,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R4884:Mycbp2
|
UTSW |
14 |
103,448,731 (GRCm39) |
missense |
probably damaging |
1.00 |
R4885:Mycbp2
|
UTSW |
14 |
103,383,382 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4956:Mycbp2
|
UTSW |
14 |
103,524,675 (GRCm39) |
missense |
probably damaging |
0.99 |
R4980:Mycbp2
|
UTSW |
14 |
103,497,821 (GRCm39) |
splice site |
probably null |
|
R4994:Mycbp2
|
UTSW |
14 |
103,407,430 (GRCm39) |
missense |
probably benign |
|
R5029:Mycbp2
|
UTSW |
14 |
103,393,946 (GRCm39) |
missense |
probably benign |
0.21 |
R5038:Mycbp2
|
UTSW |
14 |
103,534,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R5044:Mycbp2
|
UTSW |
14 |
103,376,671 (GRCm39) |
critical splice donor site |
probably null |
|
R5231:Mycbp2
|
UTSW |
14 |
103,583,650 (GRCm39) |
critical splice donor site |
probably null |
|
R5305:Mycbp2
|
UTSW |
14 |
103,583,757 (GRCm39) |
missense |
probably benign |
0.00 |
R5322:Mycbp2
|
UTSW |
14 |
103,423,119 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5376:Mycbp2
|
UTSW |
14 |
103,479,868 (GRCm39) |
nonsense |
probably null |
|
R5414:Mycbp2
|
UTSW |
14 |
103,543,697 (GRCm39) |
missense |
probably damaging |
1.00 |
R5453:Mycbp2
|
UTSW |
14 |
103,438,837 (GRCm39) |
missense |
probably damaging |
0.99 |
R5462:Mycbp2
|
UTSW |
14 |
103,437,562 (GRCm39) |
missense |
probably damaging |
1.00 |
R5499:Mycbp2
|
UTSW |
14 |
103,479,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R5502:Mycbp2
|
UTSW |
14 |
103,411,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R5524:Mycbp2
|
UTSW |
14 |
103,532,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R5533:Mycbp2
|
UTSW |
14 |
103,520,081 (GRCm39) |
nonsense |
probably null |
|
R5569:Mycbp2
|
UTSW |
14 |
103,372,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R5574:Mycbp2
|
UTSW |
14 |
103,380,203 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5579:Mycbp2
|
UTSW |
14 |
103,528,769 (GRCm39) |
missense |
probably damaging |
0.98 |
R5590:Mycbp2
|
UTSW |
14 |
103,360,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R5592:Mycbp2
|
UTSW |
14 |
103,432,113 (GRCm39) |
missense |
probably benign |
0.02 |
R5643:Mycbp2
|
UTSW |
14 |
103,524,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R5644:Mycbp2
|
UTSW |
14 |
103,524,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R5645:Mycbp2
|
UTSW |
14 |
103,426,051 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5645:Mycbp2
|
UTSW |
14 |
103,426,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R5646:Mycbp2
|
UTSW |
14 |
103,407,346 (GRCm39) |
missense |
probably benign |
0.09 |
R5648:Mycbp2
|
UTSW |
14 |
103,528,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R5651:Mycbp2
|
UTSW |
14 |
103,520,101 (GRCm39) |
missense |
probably null |
0.99 |
R5668:Mycbp2
|
UTSW |
14 |
103,357,955 (GRCm39) |
missense |
possibly damaging |
0.62 |
R5745:Mycbp2
|
UTSW |
14 |
103,393,889 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5751:Mycbp2
|
UTSW |
14 |
103,385,986 (GRCm39) |
missense |
probably damaging |
0.99 |
R5756:Mycbp2
|
UTSW |
14 |
103,371,410 (GRCm39) |
missense |
probably damaging |
0.99 |
R5837:Mycbp2
|
UTSW |
14 |
103,361,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R5984:Mycbp2
|
UTSW |
14 |
103,364,120 (GRCm39) |
missense |
probably damaging |
0.98 |
R6005:Mycbp2
|
UTSW |
14 |
103,394,159 (GRCm39) |
missense |
probably benign |
|
R6063:Mycbp2
|
UTSW |
14 |
103,372,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R6091:Mycbp2
|
UTSW |
14 |
103,460,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R6120:Mycbp2
|
UTSW |
14 |
103,513,323 (GRCm39) |
missense |
probably benign |
0.01 |
R6129:Mycbp2
|
UTSW |
14 |
103,522,836 (GRCm39) |
missense |
probably benign |
0.21 |
R6147:Mycbp2
|
UTSW |
14 |
103,392,945 (GRCm39) |
nonsense |
probably null |
|
R6161:Mycbp2
|
UTSW |
14 |
103,536,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R6187:Mycbp2
|
UTSW |
14 |
103,384,453 (GRCm39) |
missense |
probably damaging |
1.00 |
R6208:Mycbp2
|
UTSW |
14 |
103,532,664 (GRCm39) |
missense |
probably benign |
0.11 |
R6228:Mycbp2
|
UTSW |
14 |
103,497,665 (GRCm39) |
missense |
probably benign |
0.24 |
R6301:Mycbp2
|
UTSW |
14 |
103,392,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R6311:Mycbp2
|
UTSW |
14 |
103,500,176 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6329:Mycbp2
|
UTSW |
14 |
103,393,288 (GRCm39) |
missense |
probably benign |
0.00 |
R6439:Mycbp2
|
UTSW |
14 |
103,392,911 (GRCm39) |
missense |
probably benign |
0.00 |
R6462:Mycbp2
|
UTSW |
14 |
103,373,993 (GRCm39) |
critical splice donor site |
probably null |
|
R6528:Mycbp2
|
UTSW |
14 |
103,380,317 (GRCm39) |
missense |
probably damaging |
0.99 |
R6736:Mycbp2
|
UTSW |
14 |
103,429,003 (GRCm39) |
missense |
probably null |
1.00 |
R6821:Mycbp2
|
UTSW |
14 |
103,376,845 (GRCm39) |
missense |
probably damaging |
1.00 |
R6851:Mycbp2
|
UTSW |
14 |
103,497,630 (GRCm39) |
critical splice donor site |
probably null |
|
R6948:Mycbp2
|
UTSW |
14 |
103,522,703 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6977:Mycbp2
|
UTSW |
14 |
103,392,342 (GRCm39) |
missense |
probably damaging |
0.99 |
R6985:Mycbp2
|
UTSW |
14 |
103,444,117 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7035:Mycbp2
|
UTSW |
14 |
103,412,417 (GRCm39) |
missense |
probably benign |
|
R7054:Mycbp2
|
UTSW |
14 |
103,393,534 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7108:Mycbp2
|
UTSW |
14 |
103,360,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R7117:Mycbp2
|
UTSW |
14 |
103,391,513 (GRCm39) |
missense |
probably benign |
0.21 |
R7137:Mycbp2
|
UTSW |
14 |
103,520,115 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7169:Mycbp2
|
UTSW |
14 |
103,497,636 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7218:Mycbp2
|
UTSW |
14 |
103,371,282 (GRCm39) |
missense |
probably benign |
|
R7234:Mycbp2
|
UTSW |
14 |
103,452,773 (GRCm39) |
missense |
probably damaging |
0.98 |
R7238:Mycbp2
|
UTSW |
14 |
103,393,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R7244:Mycbp2
|
UTSW |
14 |
103,446,345 (GRCm39) |
missense |
probably damaging |
0.98 |
R7265:Mycbp2
|
UTSW |
14 |
103,434,679 (GRCm39) |
critical splice donor site |
probably null |
|
R7286:Mycbp2
|
UTSW |
14 |
103,358,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R7332:Mycbp2
|
UTSW |
14 |
103,434,793 (GRCm39) |
missense |
probably damaging |
0.97 |
R7332:Mycbp2
|
UTSW |
14 |
103,393,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R7384:Mycbp2
|
UTSW |
14 |
103,513,829 (GRCm39) |
missense |
probably damaging |
0.99 |
R7392:Mycbp2
|
UTSW |
14 |
103,480,564 (GRCm39) |
missense |
probably damaging |
0.99 |
R7392:Mycbp2
|
UTSW |
14 |
103,389,627 (GRCm39) |
missense |
probably damaging |
1.00 |
R7409:Mycbp2
|
UTSW |
14 |
103,526,180 (GRCm39) |
missense |
probably damaging |
1.00 |
R7486:Mycbp2
|
UTSW |
14 |
103,434,690 (GRCm39) |
missense |
probably damaging |
0.97 |
R7643:Mycbp2
|
UTSW |
14 |
103,583,701 (GRCm39) |
missense |
probably benign |
|
R7661:Mycbp2
|
UTSW |
14 |
103,450,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R7663:Mycbp2
|
UTSW |
14 |
103,429,045 (GRCm39) |
missense |
probably damaging |
0.99 |
R7730:Mycbp2
|
UTSW |
14 |
103,360,791 (GRCm39) |
missense |
probably damaging |
0.99 |
R7757:Mycbp2
|
UTSW |
14 |
103,429,055 (GRCm39) |
missense |
probably damaging |
1.00 |
R7773:Mycbp2
|
UTSW |
14 |
103,485,840 (GRCm39) |
missense |
probably damaging |
0.97 |
R7787:Mycbp2
|
UTSW |
14 |
103,364,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R7822:Mycbp2
|
UTSW |
14 |
103,376,851 (GRCm39) |
missense |
probably benign |
0.00 |
R7838:Mycbp2
|
UTSW |
14 |
103,414,729 (GRCm39) |
missense |
probably benign |
0.10 |
R7841:Mycbp2
|
UTSW |
14 |
103,384,267 (GRCm39) |
critical splice donor site |
probably null |
|
R7858:Mycbp2
|
UTSW |
14 |
103,393,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R7873:Mycbp2
|
UTSW |
14 |
103,393,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R7911:Mycbp2
|
UTSW |
14 |
103,437,621 (GRCm39) |
missense |
probably damaging |
0.99 |
R7942:Mycbp2
|
UTSW |
14 |
103,392,674 (GRCm39) |
missense |
probably damaging |
0.99 |
R7951:Mycbp2
|
UTSW |
14 |
103,452,898 (GRCm39) |
missense |
probably damaging |
0.99 |
R7958:Mycbp2
|
UTSW |
14 |
103,367,400 (GRCm39) |
missense |
probably benign |
0.00 |
R8235:Mycbp2
|
UTSW |
14 |
103,436,110 (GRCm39) |
missense |
probably damaging |
0.99 |
R8246:Mycbp2
|
UTSW |
14 |
103,392,640 (GRCm39) |
missense |
probably damaging |
0.99 |
R8338:Mycbp2
|
UTSW |
14 |
103,372,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R8343:Mycbp2
|
UTSW |
14 |
103,398,111 (GRCm39) |
splice site |
probably null |
|
R8361:Mycbp2
|
UTSW |
14 |
103,376,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R8490:Mycbp2
|
UTSW |
14 |
103,446,267 (GRCm39) |
missense |
probably benign |
0.00 |
R8524:Mycbp2
|
UTSW |
14 |
103,392,895 (GRCm39) |
missense |
probably benign |
0.23 |
R8525:Mycbp2
|
UTSW |
14 |
103,450,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R8711:Mycbp2
|
UTSW |
14 |
103,407,430 (GRCm39) |
missense |
probably benign |
0.08 |
R8735:Mycbp2
|
UTSW |
14 |
103,460,586 (GRCm39) |
missense |
probably damaging |
0.99 |
R8825:Mycbp2
|
UTSW |
14 |
103,466,871 (GRCm39) |
missense |
probably damaging |
1.00 |
R8928:Mycbp2
|
UTSW |
14 |
103,393,781 (GRCm39) |
missense |
probably benign |
|
R8974:Mycbp2
|
UTSW |
14 |
103,361,857 (GRCm39) |
missense |
probably damaging |
1.00 |
R8987:Mycbp2
|
UTSW |
14 |
103,446,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R9021:Mycbp2
|
UTSW |
14 |
103,551,752 (GRCm39) |
missense |
probably benign |
0.08 |
R9062:Mycbp2
|
UTSW |
14 |
103,479,796 (GRCm39) |
missense |
probably benign |
0.00 |
R9077:Mycbp2
|
UTSW |
14 |
103,469,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R9208:Mycbp2
|
UTSW |
14 |
103,532,664 (GRCm39) |
missense |
probably benign |
0.01 |
R9285:Mycbp2
|
UTSW |
14 |
103,434,753 (GRCm39) |
missense |
probably damaging |
0.97 |
R9290:Mycbp2
|
UTSW |
14 |
103,425,960 (GRCm39) |
missense |
probably damaging |
0.99 |
R9362:Mycbp2
|
UTSW |
14 |
103,497,642 (GRCm39) |
missense |
probably damaging |
0.97 |
R9520:Mycbp2
|
UTSW |
14 |
103,497,705 (GRCm39) |
missense |
probably benign |
0.02 |
R9557:Mycbp2
|
UTSW |
14 |
103,372,697 (GRCm39) |
missense |
probably benign |
0.03 |
R9639:Mycbp2
|
UTSW |
14 |
103,433,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R9666:Mycbp2
|
UTSW |
14 |
103,371,474 (GRCm39) |
missense |
probably damaging |
0.98 |
R9732:Mycbp2
|
UTSW |
14 |
103,448,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R9736:Mycbp2
|
UTSW |
14 |
103,434,852 (GRCm39) |
missense |
probably damaging |
0.96 |
R9739:Mycbp2
|
UTSW |
14 |
103,520,229 (GRCm39) |
missense |
probably benign |
0.11 |
R9755:Mycbp2
|
UTSW |
14 |
103,551,806 (GRCm39) |
missense |
probably benign |
|
X0024:Mycbp2
|
UTSW |
14 |
103,384,378 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Mycbp2
|
UTSW |
14 |
103,583,685 (GRCm39) |
missense |
probably benign |
|
Z1176:Mycbp2
|
UTSW |
14 |
103,394,073 (GRCm39) |
missense |
probably benign |
0.06 |
Z1177:Mycbp2
|
UTSW |
14 |
103,407,309 (GRCm39) |
missense |
possibly damaging |
0.83 |
Z1177:Mycbp2
|
UTSW |
14 |
103,372,559 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Mycbp2
|
UTSW |
14 |
103,364,499 (GRCm39) |
critical splice donor site |
probably null |
|
|