Other mutations in this stock |
Total: 243 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc4 |
G |
A |
14: 118,790,761 (GRCm39) |
R749C |
probably damaging |
Het |
Acot11 |
T |
C |
4: 106,619,232 (GRCm39) |
E201G |
probably damaging |
Het |
Adgrf4 |
C |
T |
17: 42,977,789 (GRCm39) |
R518Q |
possibly damaging |
Het |
Akap13 |
G |
T |
7: 75,261,182 (GRCm39) |
A1269S |
probably benign |
Het |
Aldh4a1 |
T |
C |
4: 139,371,439 (GRCm39) |
V451A |
probably benign |
Het |
Aox3 |
A |
G |
1: 58,209,002 (GRCm39) |
H845R |
probably damaging |
Het |
Arhgap23 |
A |
G |
11: 97,342,387 (GRCm39) |
D223G |
possibly damaging |
Het |
Asb6 |
G |
A |
2: 30,717,088 (GRCm39) |
R46W |
probably damaging |
Het |
Aspm |
A |
G |
1: 139,401,312 (GRCm39) |
I1111V |
probably benign |
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 |
Cad |
T |
A |
5: 31,215,416 (GRCm39) |
F76I |
probably damaging |
Het |
Camsap2 |
C |
T |
1: 136,209,053 (GRCm39) |
R802Q |
probably benign |
Het |
Capn11 |
A |
G |
17: 45,949,623 (GRCm39) |
S448P |
probably benign |
Het |
Capn9 |
G |
A |
8: 125,332,450 (GRCm39) |
G430R |
possibly damaging |
Het |
Cbx5 |
G |
A |
15: 103,121,551 (GRCm39) |
R29C |
probably null |
Het |
Ccdc93 |
C |
T |
1: 121,383,855 (GRCm39) |
P192L |
probably benign |
Het |
Ccdc93 |
T |
C |
1: 121,389,668 (GRCm39) |
V237A |
probably benign |
Het |
Ccn4 |
G |
A |
15: 66,778,338 (GRCm39) |
C53Y |
probably damaging |
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 |
T |
C |
1: 140,064,526 (GRCm39) |
K374R |
probably benign |
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 |
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 |
Cntnap5c |
A |
G |
17: 58,469,286 (GRCm39) |
I623V |
probably benign |
Het |
Cntrl |
CAGAG |
CAG |
2: 35,012,818 (GRCm39) |
|
probably null |
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 |
Crocc |
T |
C |
4: 140,749,113 (GRCm39) |
D1564G |
probably damaging |
Het |
Csf1r |
A |
T |
18: 61,262,149 (GRCm39) |
M802L |
probably damaging |
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 |
Daxx |
T |
C |
17: 34,130,816 (GRCm39) |
I277T |
probably damaging |
Het |
Dctn4 |
T |
C |
18: 60,679,407 (GRCm39) |
|
probably null |
Het |
Ddx59 |
T |
C |
1: 136,344,791 (GRCm39) |
V154A |
probably benign |
Het |
Dnah5 |
A |
G |
15: 28,313,932 (GRCm39) |
Q1916R |
probably damaging |
Het |
Dnah8 |
T |
C |
17: 30,941,911 (GRCm39) |
V1719A |
probably 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 |
En1 |
A |
G |
1: 120,531,350 (GRCm39) |
S197G |
unknown |
Het |
Enah |
A |
T |
1: 181,783,994 (GRCm39) |
M105K |
unknown |
Het |
Epm2a |
A |
G |
10: 11,219,426 (GRCm39) |
E71G |
probably benign |
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 |
Etnk2 |
A |
G |
1: 133,291,661 (GRCm39) |
S54G |
probably benign |
Het |
Eya1 |
A |
G |
1: 14,241,198 (GRCm39) |
V573A |
probably benign |
Het |
Faim2 |
A |
G |
15: 99,410,423 (GRCm39) |
L235P |
probably damaging |
Het |
Fam221b |
T |
A |
4: 43,665,537 (GRCm39) |
H307L |
probably damaging |
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 |
Fbxw10 |
T |
A |
11: 62,750,683 (GRCm39) |
I422N |
probably 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 |
Foxn4 |
C |
T |
5: 114,401,193 (GRCm39) |
D37N |
probably damaging |
Het |
Gabarap |
C |
T |
11: 69,882,515 (GRCm39) |
|
probably benign |
Het |
Gemin4 |
G |
C |
11: 76,101,876 (GRCm39) |
P962A |
probably damaging |
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 |
Gm10563 |
C |
T |
4: 155,720,337 (GRCm39) |
|
probably benign |
Het |
Gm28040 |
AGTG |
AGTGGCACCTTTGGTG |
1: 133,255,059 (GRCm39) |
|
probably benign |
Het |
Gm8374 |
T |
C |
14: 18,537,078 (GRCm39) |
T49A |
probably damaging |
Het |
Golim4 |
A |
T |
3: 75,815,456 (GRCm39) |
V116D |
probably damaging |
Het |
Gper1 |
C |
T |
5: 139,412,477 (GRCm39) |
P274L |
probably damaging |
Het |
Gpr132 |
A |
G |
12: 112,816,023 (GRCm39) |
S268P |
probably damaging |
Het |
Gpr25 |
G |
A |
1: 136,188,448 (GRCm39) |
P55L |
probably benign |
Het |
Grm7 |
G |
C |
6: 111,335,256 (GRCm39) |
D556H |
probably damaging |
Het |
H2-K2 |
C |
A |
17: 34,216,322 (GRCm39) |
E275* |
probably null |
Het |
Ift20 |
G |
A |
11: 78,430,860 (GRCm39) |
E68K |
probably damaging |
Het |
Igfn1 |
T |
C |
1: 135,926,421 (GRCm39) |
I10V |
unknown |
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 |
G |
A |
1: 135,887,666 (GRCm39) |
P2466L |
probably damaging |
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 |
Ikbke |
C |
A |
1: 131,193,674 (GRCm39) |
A459S |
probably benign |
Het |
Ikbke |
T |
C |
1: 131,197,560 (GRCm39) |
S447G |
probably benign |
Het |
Insrr |
G |
A |
3: 87,717,879 (GRCm39) |
|
probably null |
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 |
TCC |
TCCGCC |
1: 135,314,019 (GRCm39) |
|
probably benign |
Het |
Jarid2 |
T |
A |
13: 45,059,752 (GRCm39) |
N661K |
probably damaging |
Het |
Kcnt2 |
G |
A |
1: 140,282,285 (GRCm39) |
S90N |
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 |
Kif14 |
A |
G |
1: 136,396,017 (GRCm39) |
N108D |
probably benign |
Het |
Kmt2a |
G |
A |
9: 44,730,972 (GRCm39) |
|
probably benign |
Het |
Krtap16-1 |
A |
T |
11: 99,876,602 (GRCm39) |
C267* |
probably null |
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 |
A |
T |
1: 134,915,747 (GRCm39) |
S334T |
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 |
Lhx6 |
G |
T |
2: 35,977,470 (GRCm39) |
C327* |
probably null |
Het |
Lifr |
A |
G |
15: 7,211,337 (GRCm39) |
D625G |
possibly damaging |
Het |
Lman1 |
A |
T |
18: 66,124,653 (GRCm39) |
M362K |
probably damaging |
Het |
Lmod1 |
C |
T |
1: 135,291,811 (GRCm39) |
T222I |
probably benign |
Het |
Lmtk2 |
C |
T |
5: 144,111,806 (GRCm39) |
T842I |
possibly damaging |
Het |
Lpin3 |
T |
A |
2: 160,738,729 (GRCm39) |
L227* |
probably null |
Het |
Magel2 |
A |
T |
7: 62,027,486 (GRCm39) |
H130L |
unknown |
Het |
Mki67 |
T |
A |
7: 135,305,970 (GRCm39) |
|
probably null |
Het |
Mnx1 |
T |
A |
5: 29,679,187 (GRCm39) |
S299C |
unknown |
Het |
Mov10 |
A |
T |
3: 104,725,432 (GRCm39) |
I59N |
possibly damaging |
Het |
Mpo |
A |
G |
11: 87,688,187 (GRCm39) |
D282G |
possibly damaging |
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 |
Myo7b |
T |
C |
18: 32,127,950 (GRCm39) |
I581V |
probably benign |
Het |
Nav1 |
A |
T |
1: 135,512,465 (GRCm39) |
D198E |
possibly damaging |
Het |
Ncdn |
T |
A |
4: 126,639,066 (GRCm39) |
|
probably null |
Het |
Ndufa4 |
A |
T |
6: 11,900,574 (GRCm39) |
V37E |
probably benign |
Het |
Nop9 |
T |
C |
14: 55,988,599 (GRCm39) |
L347P |
probably damaging |
Het |
Nr5a2 |
C |
A |
1: 136,879,863 (GRCm39) |
R35L |
probably benign |
Het |
Nrp1 |
A |
T |
8: 129,224,997 (GRCm39) |
E782D |
probably damaging |
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 |
Or11m3 |
A |
T |
15: 98,395,716 (GRCm39) |
D121V |
probably damaging |
Het |
Or1j13 |
A |
G |
2: 36,370,059 (GRCm39) |
S28P |
possibly damaging |
Het |
Or2z8 |
A |
G |
8: 72,812,280 (GRCm39) |
Y252C |
probably damaging |
Het |
Or4a68 |
C |
T |
2: 89,269,927 (GRCm39) |
R232H |
probably benign |
Het |
Or5k3 |
A |
G |
16: 58,969,660 (GRCm39) |
Y149C |
probably damaging |
Het |
Pard6g |
T |
C |
18: 80,160,523 (GRCm39) |
V212A |
probably damaging |
Het |
Pbx1 |
T |
G |
1: 168,258,947 (GRCm39) |
I43L |
probably benign |
Het |
Phf2 |
T |
C |
13: 48,971,043 (GRCm39) |
D543G |
unknown |
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 |
Pkd1 |
T |
C |
17: 24,810,073 (GRCm39) |
V3558A |
probably benign |
Het |
Pla2g6 |
T |
C |
15: 79,190,545 (GRCm39) |
Y339C |
probably benign |
Het |
Plcb1 |
T |
A |
2: 135,167,587 (GRCm39) |
Y460* |
probably null |
Het |
Plekha6 |
C |
G |
1: 133,215,584 (GRCm39) |
T792S |
probably benign |
Het |
Ppard |
T |
G |
17: 28,517,455 (GRCm39) |
|
probably null |
Het |
Ppfia4 |
G |
A |
1: 134,227,059 (GRCm39) |
P1159S |
probably benign |
Het |
Ppm1f |
A |
G |
16: 16,728,834 (GRCm39) |
T79A |
probably benign |
Het |
Prelp |
C |
T |
1: 133,842,869 (GRCm39) |
R92K |
probably benign |
Het |
Ptgdr |
A |
T |
14: 45,096,036 (GRCm39) |
Y225* |
probably null |
Het |
Ptpn22 |
A |
G |
3: 103,781,368 (GRCm39) |
I90V |
probably damaging |
Het |
Ptpn7 |
A |
G |
1: 135,062,213 (GRCm39) |
Q53R |
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 |
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 |
Pus7l |
T |
C |
15: 94,438,518 (GRCm39) |
N109S |
probably benign |
Het |
Rab29 |
A |
G |
1: 131,799,848 (GRCm39) |
Q141R |
probably benign |
Het |
Ren1 |
T |
A |
1: 133,281,944 (GRCm39) |
W22R |
probably damaging |
Het |
Ren1 |
C |
G |
1: 133,278,516 (GRCm39) |
|
probably null |
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 |
T |
1: 133,281,975 (GRCm39) |
T32I |
probably benign |
Het |
Rfwd3 |
A |
T |
8: 112,024,034 (GRCm39) |
V96E |
probably benign |
Het |
Ripk4 |
A |
C |
16: 97,551,331 (GRCm39) |
V149G |
probably damaging |
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 |
Rora |
G |
A |
9: 69,284,119 (GRCm39) |
A396T |
probably benign |
Het |
Scap |
C |
T |
9: 110,203,123 (GRCm39) |
L266F |
probably damaging |
Het |
Scn5a |
A |
T |
9: 119,350,195 (GRCm39) |
I893N |
probably damaging |
Het |
Sctr |
T |
C |
1: 119,959,386 (GRCm39) |
F110L |
probably benign |
Het |
Sctr |
G |
A |
1: 119,990,987 (GRCm39) |
S440N |
possibly damaging |
Het |
Sctr |
G |
T |
1: 119,990,976 (GRCm39) |
E453D |
probably benign |
Het |
Septin4 |
A |
T |
11: 87,474,262 (GRCm39) |
Q60L |
probably benign |
Het |
Serpinb10 |
C |
T |
1: 107,466,203 (GRCm39) |
S63F |
probably damaging |
Het |
Serpinb2 |
C |
T |
1: 107,451,620 (GRCm39) |
H258Y |
probably benign |
Het |
Serpinb2 |
C |
T |
1: 107,451,624 (GRCm39) |
T259I |
probably benign |
Het |
Serpinb2 |
A |
C |
1: 107,452,273 (GRCm39) |
S284R |
probably benign |
Het |
Serpinb2 |
G |
A |
1: 107,443,365 (GRCm39) |
A55T |
probably damaging |
Het |
Serpinb2 |
C |
A |
1: 107,451,564 (GRCm39) |
A239E |
probably benign |
Het |
Serpinb8 |
A |
C |
1: 107,534,734 (GRCm39) |
L268F |
probably benign |
Het |
Serpinb8 |
A |
G |
1: 107,525,257 (GRCm39) |
S20G |
probably benign |
Het |
Serpinb8 |
G |
A |
1: 107,526,684 (GRCm39) |
A75T |
probably benign |
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 |
Slc9a4 |
T |
G |
1: 40,646,901 (GRCm39) |
|
probably null |
Het |
Slc9a9 |
A |
T |
9: 94,901,246 (GRCm39) |
N393I |
possibly damaging |
Het |
Stard13 |
T |
C |
5: 150,968,633 (GRCm39) |
Y879C |
probably damaging |
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 |
Synj1 |
G |
T |
16: 90,761,405 (GRCm39) |
A687D |
probably damaging |
Het |
Tacc1 |
A |
T |
8: 25,654,509 (GRCm39) |
N271K |
probably damaging |
Het |
Tbx1 |
A |
C |
16: 18,403,879 (GRCm39) |
F138V |
probably damaging |
Het |
Tecpr1 |
T |
A |
5: 144,145,463 (GRCm39) |
T595S |
probably benign |
Het |
Thsd7b |
T |
A |
1: 129,595,674 (GRCm39) |
F498Y |
probably benign |
Het |
Thsd7b |
C |
T |
1: 129,556,628 (GRCm39) |
T328I |
probably damaging |
Het |
Thsd7b |
A |
C |
1: 130,044,368 (GRCm39) |
Q1116P |
probably benign |
Het |
Thsd7b |
G |
C |
1: 129,605,920 (GRCm39) |
A554P |
probably benign |
Het |
Tnnt2 |
C |
T |
1: 135,773,244 (GRCm39) |
|
probably benign |
Het |
Trappc8 |
A |
G |
18: 20,967,997 (GRCm39) |
|
probably null |
Het |
Trim33 |
AGACTG |
A |
3: 103,236,536 (GRCm39) |
|
probably null |
Het |
Trim41 |
C |
A |
11: 48,698,419 (GRCm39) |
G516W |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,643,683 (GRCm39) |
G11436R |
probably damaging |
Het |
Ttn |
A |
C |
2: 76,716,270 (GRCm39) |
|
probably null |
Het |
Txk |
T |
A |
5: 72,853,922 (GRCm39) |
T472S |
probably damaging |
Het |
Ube2t |
C |
T |
1: 134,899,905 (GRCm39) |
A149V |
probably benign |
Het |
Ubr4 |
T |
A |
4: 139,151,256 (GRCm39) |
M1897K |
probably damaging |
Het |
Uggt2 |
A |
G |
14: 119,298,788 (GRCm39) |
L391P |
probably damaging |
Het |
Vmn2r55 |
A |
T |
7: 12,402,111 (GRCm39) |
D392E |
probably damaging |
Het |
Vps13b |
A |
G |
15: 35,879,937 (GRCm39) |
Y3004C |
probably damaging |
Het |
Vps26a |
A |
T |
10: 62,304,176 (GRCm39) |
D180E |
probably benign |
Het |
Vps35l |
T |
C |
7: 118,393,798 (GRCm39) |
Y516H |
probably damaging |
Het |
Xirp1 |
T |
G |
9: 120,016,907 (GRCm38) |
Q970P |
probably benign |
Het |
Zbtb46 |
C |
T |
2: 181,033,224 (GRCm39) |
C479Y |
probably damaging |
Het |
Zc3h11a |
G |
A |
1: 133,549,892 (GRCm39) |
P695S |
probably benign |
Het |
Zc3h11a |
C |
T |
1: 133,552,359 (GRCm39) |
V583I |
probably benign |
Het |
Zdhhc13 |
T |
A |
7: 48,474,392 (GRCm39) |
L548Q |
possibly damaging |
Het |
Zfp236 |
T |
C |
18: 82,639,429 (GRCm39) |
M1225V |
probably benign |
Het |
Zfp281 |
GCGGCAGCTCCGGCAGC |
GCGGCAGCTCCGGCAGCTCCGGCAGC |
1: 136,553,091 (GRCm39) |
|
probably benign |
Het |
Zp3r |
C |
A |
1: 130,547,151 (GRCm39) |
E8D |
possibly damaging |
Het |
Zp3r |
A |
G |
1: 130,524,551 (GRCm39) |
L164P |
probably benign |
Het |
|
Other mutations in Zfyve26 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00090:Zfyve26
|
APN |
12 |
79,296,234 (GRCm39) |
unclassified |
probably benign |
|
IGL00940:Zfyve26
|
APN |
12 |
79,327,674 (GRCm39) |
missense |
probably benign |
|
IGL01148:Zfyve26
|
APN |
12 |
79,307,644 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01347:Zfyve26
|
APN |
12 |
79,298,957 (GRCm39) |
splice site |
probably null |
|
IGL01472:Zfyve26
|
APN |
12 |
79,323,117 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01490:Zfyve26
|
APN |
12 |
79,291,147 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01516:Zfyve26
|
APN |
12 |
79,334,625 (GRCm39) |
missense |
probably benign |
0.37 |
IGL01642:Zfyve26
|
APN |
12 |
79,308,348 (GRCm39) |
splice site |
probably null |
|
IGL01689:Zfyve26
|
APN |
12 |
79,330,827 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL01877:Zfyve26
|
APN |
12 |
79,334,218 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01997:Zfyve26
|
APN |
12 |
79,291,174 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02077:Zfyve26
|
APN |
12 |
79,323,169 (GRCm39) |
missense |
possibly damaging |
0.54 |
IGL02437:Zfyve26
|
APN |
12 |
79,315,621 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02933:Zfyve26
|
APN |
12 |
79,326,854 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02937:Zfyve26
|
APN |
12 |
79,285,794 (GRCm39) |
missense |
probably benign |
0.08 |
IGL02982:Zfyve26
|
APN |
12 |
79,310,644 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03064:Zfyve26
|
APN |
12 |
79,308,565 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03086:Zfyve26
|
APN |
12 |
79,342,338 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03146:Zfyve26
|
APN |
12 |
79,330,846 (GRCm39) |
nonsense |
probably null |
|
challenge
|
UTSW |
12 |
79,317,610 (GRCm39) |
critical splice donor site |
probably null |
|
fourteener
|
UTSW |
12 |
79,302,037 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02799:Zfyve26
|
UTSW |
12 |
79,320,084 (GRCm39) |
missense |
probably benign |
0.28 |
R0318:Zfyve26
|
UTSW |
12 |
79,323,055 (GRCm39) |
missense |
probably damaging |
1.00 |
R0513:Zfyve26
|
UTSW |
12 |
79,291,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R0582:Zfyve26
|
UTSW |
12 |
79,292,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R0586:Zfyve26
|
UTSW |
12 |
79,315,502 (GRCm39) |
missense |
possibly damaging |
0.96 |
R0718:Zfyve26
|
UTSW |
12 |
79,312,576 (GRCm39) |
splice site |
probably benign |
|
R0738:Zfyve26
|
UTSW |
12 |
79,342,308 (GRCm39) |
missense |
probably damaging |
1.00 |
R0781:Zfyve26
|
UTSW |
12 |
79,326,841 (GRCm39) |
missense |
probably damaging |
0.99 |
R0894:Zfyve26
|
UTSW |
12 |
79,320,372 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1109:Zfyve26
|
UTSW |
12 |
79,318,901 (GRCm39) |
missense |
probably damaging |
1.00 |
R1110:Zfyve26
|
UTSW |
12 |
79,326,841 (GRCm39) |
missense |
probably damaging |
0.99 |
R1186:Zfyve26
|
UTSW |
12 |
79,310,723 (GRCm39) |
missense |
probably damaging |
1.00 |
R1295:Zfyve26
|
UTSW |
12 |
79,321,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R1430:Zfyve26
|
UTSW |
12 |
79,329,591 (GRCm39) |
missense |
probably benign |
0.07 |
R1439:Zfyve26
|
UTSW |
12 |
79,298,937 (GRCm39) |
missense |
probably benign |
0.03 |
R1517:Zfyve26
|
UTSW |
12 |
79,298,925 (GRCm39) |
missense |
probably damaging |
0.98 |
R1553:Zfyve26
|
UTSW |
12 |
79,334,535 (GRCm39) |
missense |
probably benign |
0.00 |
R1721:Zfyve26
|
UTSW |
12 |
79,308,573 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1758:Zfyve26
|
UTSW |
12 |
79,285,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R1779:Zfyve26
|
UTSW |
12 |
79,325,237 (GRCm39) |
missense |
probably damaging |
1.00 |
R1786:Zfyve26
|
UTSW |
12 |
79,315,208 (GRCm39) |
missense |
possibly damaging |
0.48 |
R1826:Zfyve26
|
UTSW |
12 |
79,315,823 (GRCm39) |
missense |
probably damaging |
1.00 |
R1833:Zfyve26
|
UTSW |
12 |
79,333,032 (GRCm39) |
missense |
probably benign |
0.36 |
R1868:Zfyve26
|
UTSW |
12 |
79,308,573 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1900:Zfyve26
|
UTSW |
12 |
79,311,125 (GRCm39) |
missense |
probably damaging |
1.00 |
R1928:Zfyve26
|
UTSW |
12 |
79,286,744 (GRCm39) |
nonsense |
probably null |
|
R1982:Zfyve26
|
UTSW |
12 |
79,302,017 (GRCm39) |
missense |
possibly damaging |
0.55 |
R2062:Zfyve26
|
UTSW |
12 |
79,330,806 (GRCm39) |
splice site |
probably null |
|
R2071:Zfyve26
|
UTSW |
12 |
79,334,220 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2130:Zfyve26
|
UTSW |
12 |
79,315,208 (GRCm39) |
missense |
possibly damaging |
0.48 |
R2132:Zfyve26
|
UTSW |
12 |
79,315,208 (GRCm39) |
missense |
possibly damaging |
0.48 |
R2133:Zfyve26
|
UTSW |
12 |
79,315,208 (GRCm39) |
missense |
possibly damaging |
0.48 |
R2135:Zfyve26
|
UTSW |
12 |
79,292,826 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2207:Zfyve26
|
UTSW |
12 |
79,292,861 (GRCm39) |
missense |
probably damaging |
0.99 |
R2280:Zfyve26
|
UTSW |
12 |
79,321,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R2352:Zfyve26
|
UTSW |
12 |
79,330,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R2398:Zfyve26
|
UTSW |
12 |
79,329,573 (GRCm39) |
splice site |
probably null |
|
R3084:Zfyve26
|
UTSW |
12 |
79,312,457 (GRCm39) |
splice site |
probably benign |
|
R3086:Zfyve26
|
UTSW |
12 |
79,312,457 (GRCm39) |
splice site |
probably benign |
|
R4626:Zfyve26
|
UTSW |
12 |
79,315,844 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4727:Zfyve26
|
UTSW |
12 |
79,291,170 (GRCm39) |
missense |
probably benign |
0.16 |
R4908:Zfyve26
|
UTSW |
12 |
79,296,469 (GRCm39) |
splice site |
probably null |
|
R4926:Zfyve26
|
UTSW |
12 |
79,321,785 (GRCm39) |
missense |
probably benign |
|
R4990:Zfyve26
|
UTSW |
12 |
79,334,607 (GRCm39) |
missense |
probably damaging |
1.00 |
R4999:Zfyve26
|
UTSW |
12 |
79,327,159 (GRCm39) |
nonsense |
probably null |
|
R5029:Zfyve26
|
UTSW |
12 |
79,333,097 (GRCm39) |
missense |
probably damaging |
0.99 |
R5070:Zfyve26
|
UTSW |
12 |
79,302,135 (GRCm39) |
missense |
probably damaging |
1.00 |
R5100:Zfyve26
|
UTSW |
12 |
79,326,832 (GRCm39) |
nonsense |
probably null |
|
R5252:Zfyve26
|
UTSW |
12 |
79,315,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R5318:Zfyve26
|
UTSW |
12 |
79,317,624 (GRCm39) |
missense |
probably benign |
0.35 |
R5509:Zfyve26
|
UTSW |
12 |
79,293,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R5574:Zfyve26
|
UTSW |
12 |
79,286,698 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5735:Zfyve26
|
UTSW |
12 |
79,320,147 (GRCm39) |
missense |
probably damaging |
0.96 |
R5756:Zfyve26
|
UTSW |
12 |
79,311,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R5773:Zfyve26
|
UTSW |
12 |
79,334,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R5834:Zfyve26
|
UTSW |
12 |
79,313,311 (GRCm39) |
missense |
probably benign |
0.30 |
R6075:Zfyve26
|
UTSW |
12 |
79,340,628 (GRCm39) |
missense |
possibly damaging |
0.74 |
R6184:Zfyve26
|
UTSW |
12 |
79,315,501 (GRCm39) |
missense |
probably damaging |
0.98 |
R6235:Zfyve26
|
UTSW |
12 |
79,296,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R6247:Zfyve26
|
UTSW |
12 |
79,329,758 (GRCm39) |
missense |
probably benign |
0.04 |
R6320:Zfyve26
|
UTSW |
12 |
79,286,776 (GRCm39) |
missense |
probably damaging |
0.97 |
R6548:Zfyve26
|
UTSW |
12 |
79,285,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R6887:Zfyve26
|
UTSW |
12 |
79,313,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R7133:Zfyve26
|
UTSW |
12 |
79,330,926 (GRCm39) |
missense |
probably benign |
0.06 |
R7152:Zfyve26
|
UTSW |
12 |
79,325,888 (GRCm39) |
missense |
probably benign |
0.42 |
R7165:Zfyve26
|
UTSW |
12 |
79,327,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R7181:Zfyve26
|
UTSW |
12 |
79,315,182 (GRCm39) |
missense |
probably benign |
0.00 |
R7223:Zfyve26
|
UTSW |
12 |
79,292,945 (GRCm39) |
missense |
probably damaging |
0.99 |
R7296:Zfyve26
|
UTSW |
12 |
79,325,146 (GRCm39) |
splice site |
probably null |
|
R7299:Zfyve26
|
UTSW |
12 |
79,329,758 (GRCm39) |
missense |
probably benign |
0.01 |
R7301:Zfyve26
|
UTSW |
12 |
79,329,758 (GRCm39) |
missense |
probably benign |
0.01 |
R7302:Zfyve26
|
UTSW |
12 |
79,297,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R7355:Zfyve26
|
UTSW |
12 |
79,286,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R7466:Zfyve26
|
UTSW |
12 |
79,334,581 (GRCm39) |
missense |
probably benign |
0.00 |
R7540:Zfyve26
|
UTSW |
12 |
79,315,450 (GRCm39) |
missense |
probably damaging |
0.99 |
R7552:Zfyve26
|
UTSW |
12 |
79,337,731 (GRCm39) |
missense |
probably damaging |
0.97 |
R7762:Zfyve26
|
UTSW |
12 |
79,315,409 (GRCm39) |
missense |
probably benign |
0.02 |
R7806:Zfyve26
|
UTSW |
12 |
79,327,129 (GRCm39) |
critical splice donor site |
probably null |
|
R7821:Zfyve26
|
UTSW |
12 |
79,302,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R8141:Zfyve26
|
UTSW |
12 |
79,315,331 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8190:Zfyve26
|
UTSW |
12 |
79,327,610 (GRCm39) |
missense |
probably benign |
0.00 |
R8207:Zfyve26
|
UTSW |
12 |
79,307,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R8210:Zfyve26
|
UTSW |
12 |
79,302,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R8500:Zfyve26
|
UTSW |
12 |
79,334,454 (GRCm39) |
missense |
probably damaging |
0.99 |
R8686:Zfyve26
|
UTSW |
12 |
79,334,227 (GRCm39) |
missense |
probably benign |
|
R8758:Zfyve26
|
UTSW |
12 |
79,311,083 (GRCm39) |
critical splice donor site |
probably benign |
|
R8826:Zfyve26
|
UTSW |
12 |
79,285,742 (GRCm39) |
missense |
probably benign |
0.05 |
R8877:Zfyve26
|
UTSW |
12 |
79,334,152 (GRCm39) |
missense |
probably benign |
0.05 |
R9067:Zfyve26
|
UTSW |
12 |
79,318,915 (GRCm39) |
missense |
probably damaging |
0.99 |
R9195:Zfyve26
|
UTSW |
12 |
79,311,168 (GRCm39) |
missense |
probably benign |
0.12 |
R9269:Zfyve26
|
UTSW |
12 |
79,323,076 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9273:Zfyve26
|
UTSW |
12 |
79,317,610 (GRCm39) |
critical splice donor site |
probably null |
|
R9340:Zfyve26
|
UTSW |
12 |
79,321,680 (GRCm39) |
nonsense |
probably null |
|
R9348:Zfyve26
|
UTSW |
12 |
79,315,231 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9482:Zfyve26
|
UTSW |
12 |
79,291,239 (GRCm39) |
missense |
probably damaging |
1.00 |
R9536:Zfyve26
|
UTSW |
12 |
79,298,046 (GRCm39) |
missense |
probably benign |
0.32 |
R9653:Zfyve26
|
UTSW |
12 |
79,334,418 (GRCm39) |
missense |
probably benign |
|
R9676:Zfyve26
|
UTSW |
12 |
79,330,959 (GRCm39) |
missense |
probably benign |
0.01 |
R9797:Zfyve26
|
UTSW |
12 |
79,293,006 (GRCm39) |
missense |
probably damaging |
0.98 |
RF010:Zfyve26
|
UTSW |
12 |
79,302,112 (GRCm39) |
missense |
probably damaging |
1.00 |
X0020:Zfyve26
|
UTSW |
12 |
79,285,779 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Zfyve26
|
UTSW |
12 |
79,315,307 (GRCm39) |
missense |
probably benign |
0.07 |
Z1177:Zfyve26
|
UTSW |
12 |
79,334,149 (GRCm39) |
missense |
probably null |
1.00 |
|