Other mutations in this stock |
Total: 226 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921539E11Rik |
T |
A |
4: 103,088,286 (GRCm39) |
T307S |
probably damaging |
Het |
4930590J08Rik |
T |
C |
6: 91,896,259 (GRCm39) |
I369T |
possibly damaging |
Het |
Abhd17a |
T |
A |
10: 80,419,860 (GRCm39) |
I115F |
probably benign |
Het |
Acacb |
TGGGG |
TGGG |
5: 114,347,828 (GRCm39) |
|
probably null |
Het |
Adgrb2 |
C |
T |
4: 129,903,098 (GRCm39) |
T566I |
possibly damaging |
Het |
Adgrf4 |
C |
T |
17: 42,977,789 (GRCm39) |
R518Q |
possibly damaging |
Het |
Aspm |
A |
G |
1: 139,401,312 (GRCm39) |
I1111V |
probably benign |
Het |
Bbs9 |
T |
C |
9: 22,570,415 (GRCm39) |
V587A |
possibly 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 |
Capn8 |
T |
C |
1: 182,426,387 (GRCm39) |
S241P |
probably damaging |
Het |
Capn9 |
G |
A |
8: 125,332,450 (GRCm39) |
G430R |
possibly damaging |
Het |
Cars1 |
C |
A |
7: 143,146,211 (GRCm39) |
R71M |
probably damaging |
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 |
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 |
Cep350 |
A |
C |
1: 155,804,611 (GRCm39) |
L824R |
probably 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 |
Chit1 |
A |
G |
1: 134,077,132 (GRCm39) |
R312G |
possibly damaging |
Het |
Chit1 |
G |
T |
1: 134,077,133 (GRCm39) |
R312I |
probably benign |
Het |
Cntnap5a |
C |
T |
1: 116,382,873 (GRCm39) |
T1047I |
probably benign |
Het |
Cntnap5a |
T |
C |
1: 116,382,831 (GRCm39) |
L1033S |
probably benign |
Het |
Cntnap5a |
C |
A |
1: 116,382,734 (GRCm39) |
L1001I |
probably benign |
Het |
Crb1 |
T |
C |
1: 139,162,517 (GRCm39) |
M1214V |
probably benign |
Het |
Crb1 |
C |
T |
1: 139,171,155 (GRCm39) |
R684H |
probably benign |
Het |
Crb1 |
C |
T |
1: 139,170,733 (GRCm39) |
G825R |
probably damaging |
Het |
Crb1 |
G |
A |
1: 139,168,876 (GRCm39) |
P881S |
probably damaging |
Het |
Crb1 |
A |
T |
1: 139,165,360 (GRCm39) |
H921Q |
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 |
Dsel |
G |
C |
1: 111,787,724 (GRCm39) |
T937S |
probably benign |
Het |
Dsel |
T |
C |
1: 111,787,187 (GRCm39) |
N1116S |
probably benign |
Het |
Dsg2 |
G |
A |
18: 20,724,937 (GRCm39) |
V448I |
probably benign |
Het |
Dstyk |
C |
T |
1: 132,384,722 (GRCm39) |
L739F |
probably damaging |
Het |
Efnb2 |
G |
T |
8: 8,673,237 (GRCm39) |
T140K |
probably damaging |
Het |
En1 |
A |
G |
1: 120,531,350 (GRCm39) |
S197G |
unknown |
Het |
Eogt |
T |
C |
6: 97,090,825 (GRCm39) |
D438G |
probably damaging |
Het |
Etnk2 |
A |
G |
1: 133,291,661 (GRCm39) |
S54G |
probably benign |
Het |
Etnk2 |
G |
T |
1: 133,304,784 (GRCm39) |
A336S |
probably benign |
Het |
Etnk2 |
T |
A |
1: 133,304,653 (GRCm39) |
V292E |
probably benign |
Het |
Etnk2 |
G |
A |
1: 133,293,555 (GRCm39) |
R166Q |
probably benign |
Het |
Etnk2 |
C |
T |
1: 133,293,554 (GRCm39) |
R166* |
probably null |
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 |
Etnppl |
A |
G |
3: 130,414,398 (GRCm39) |
T98A |
probably damaging |
Het |
Fam131b |
T |
G |
6: 42,295,514 (GRCm39) |
Q221P |
possibly 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 |
Fam90a1a |
A |
G |
8: 22,453,479 (GRCm39) |
N278S |
probably benign |
Het |
Fbxo40 |
T |
A |
16: 36,786,584 (GRCm39) |
M662L |
probably damaging |
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 |
C |
1: 130,732,364 (GRCm39) |
N117T |
probably benign |
Het |
Fcamr |
A |
G |
1: 130,739,317 (GRCm39) |
I206V |
probably benign |
Het |
Fcmr |
A |
G |
1: 130,803,711 (GRCm39) |
T172A |
probably benign |
Het |
Fcmr |
T |
C |
1: 130,806,006 (GRCm39) |
S321P |
probably benign |
Het |
Fmo9 |
A |
T |
1: 166,501,217 (GRCm39) |
F192L |
probably benign |
Het |
Gabarap |
C |
T |
11: 69,882,515 (GRCm39) |
|
probably benign |
Het |
Gatad2a |
G |
T |
8: 70,362,586 (GRCm39) |
H600N |
probably damaging |
Het |
Gemin4 |
G |
C |
11: 76,101,876 (GRCm39) |
P962A |
probably damaging |
Het |
Git2 |
T |
C |
5: 114,877,185 (GRCm39) |
E99G |
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 |
Gm10961 |
T |
C |
3: 107,540,310 (GRCm39) |
|
probably benign |
Het |
Gpr25 |
G |
A |
1: 136,188,448 (GRCm39) |
P55L |
probably benign |
Het |
Gpsm3 |
G |
A |
17: 34,809,728 (GRCm39) |
R52H |
possibly damaging |
Het |
Grm7 |
G |
C |
6: 111,335,256 (GRCm39) |
D556H |
probably damaging |
Het |
Hdac5 |
A |
G |
11: 102,091,342 (GRCm39) |
F683L |
probably benign |
Het |
Ift20 |
G |
A |
11: 78,430,860 (GRCm39) |
E68K |
probably 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 |
C |
A |
1: 131,193,674 (GRCm39) |
A459S |
probably benign |
Het |
Ikbke |
T |
C |
1: 131,197,560 (GRCm39) |
S447G |
probably benign |
Het |
Ipo9 |
ATCCTCCTCCTCCTCCTC |
ATCCTCCTCCTCCTCCTCCTC |
1: 135,314,006 (GRCm39) |
|
probably benign |
Het |
Ipo9 |
A |
G |
1: 135,329,988 (GRCm39) |
V484A |
probably benign |
Het |
Irx5 |
A |
C |
8: 93,086,316 (GRCm39) |
E133A |
probably damaging |
Het |
Itgb5 |
C |
T |
16: 33,760,932 (GRCm39) |
T589I |
probably benign |
Het |
Jarid2 |
T |
A |
13: 45,059,752 (GRCm39) |
N661K |
probably damaging |
Het |
Kcna5 |
A |
T |
6: 126,510,823 (GRCm39) |
I435N |
probably damaging |
Het |
Kcnj5 |
T |
C |
9: 32,233,488 (GRCm39) |
I276V |
probably damaging |
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 |
Krt1c |
T |
C |
15: 101,722,408 (GRCm39) |
R426G |
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 |
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 |
Lgr6 |
A |
T |
1: 134,915,747 (GRCm39) |
S334T |
probably benign |
Het |
Lin7b |
A |
T |
7: 45,019,351 (GRCm39) |
H72Q |
probably benign |
Het |
Lmod1 |
C |
T |
1: 135,291,811 (GRCm39) |
T222I |
probably benign |
Het |
Map3k9 |
A |
T |
12: 81,769,000 (GRCm39) |
V1016E |
probably damaging |
Het |
Mcam |
T |
C |
9: 44,046,003 (GRCm39) |
L6P |
probably damaging |
Het |
Mgam |
A |
G |
6: 40,641,794 (GRCm39) |
H549R |
possibly damaging |
Het |
Miip |
G |
A |
4: 147,950,231 (GRCm39) |
P122S |
probably damaging |
Het |
Mkrn1 |
T |
A |
6: 39,377,390 (GRCm39) |
N282Y |
probably null |
Het |
Mrc1 |
T |
C |
2: 14,332,655 (GRCm39) |
V1285A |
probably benign |
Het |
Mroh3 |
G |
C |
1: 136,119,882 (GRCm39) |
Q440E |
possibly damaging |
Het |
Mybpc1 |
T |
C |
10: 88,406,430 (GRCm39) |
D152G |
probably damaging |
Het |
Mybph |
C |
T |
1: 134,125,218 (GRCm39) |
R249C |
probably benign |
Het |
Myh7b |
A |
G |
2: 155,467,592 (GRCm39) |
D739G |
possibly damaging |
Het |
Nav1 |
A |
T |
1: 135,512,465 (GRCm39) |
D198E |
possibly damaging |
Het |
Nfkbib |
A |
T |
7: 28,461,480 (GRCm39) |
Y86N |
probably damaging |
Het |
Nr5a2 |
C |
A |
1: 136,879,863 (GRCm39) |
R35L |
probably benign |
Het |
Nrip1 |
G |
T |
16: 76,089,778 (GRCm39) |
T593K |
probably benign |
Het |
Obscn |
A |
G |
11: 58,964,459 (GRCm39) |
Y726H |
probably damaging |
Het |
Obsl1 |
G |
A |
1: 75,486,756 (GRCm38) |
T1764M |
probably benign |
Het |
Optc |
C |
G |
1: 133,832,908 (GRCm39) |
S64T |
probably benign |
Het |
Optc |
A |
T |
1: 133,831,534 (GRCm39) |
|
probably null |
Het |
Or4a68 |
C |
T |
2: 89,269,927 (GRCm39) |
R232H |
probably benign |
Het |
Or4f14b |
T |
C |
2: 111,775,633 (GRCm39) |
H56R |
probably benign |
Het |
Or8d2 |
T |
A |
9: 38,760,268 (GRCm39) |
I286K |
probably damaging |
Het |
Or8g32 |
T |
C |
9: 39,305,518 (GRCm39) |
Y144H |
probably benign |
Het |
Pard6g |
T |
A |
18: 80,123,040 (GRCm39) |
F25I |
probably damaging |
Het |
Parp6 |
C |
A |
9: 59,540,821 (GRCm39) |
C291* |
probably null |
Het |
Perm1 |
C |
T |
4: 156,302,988 (GRCm39) |
R511* |
probably null |
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 |
Plekha6 |
C |
G |
1: 133,215,584 (GRCm39) |
T792S |
probably benign |
Het |
Pole |
T |
A |
5: 110,445,296 (GRCm39) |
L481Q |
probably damaging |
Het |
Polr2i |
T |
C |
7: 29,932,493 (GRCm39) |
C67R |
probably damaging |
Het |
Ppfia4 |
G |
A |
1: 134,227,059 (GRCm39) |
P1159S |
probably benign |
Het |
Pramel31 |
G |
T |
4: 144,088,295 (GRCm39) |
E30D |
probably benign |
Het |
Prelp |
C |
T |
1: 133,842,869 (GRCm39) |
R92K |
probably benign |
Het |
Ptgfrn |
T |
C |
3: 100,963,758 (GRCm39) |
N618S |
possibly 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 |
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 |
Rims1 |
C |
T |
1: 22,416,753 (GRCm39) |
|
probably null |
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 |
Rps19bp1 |
CCTTCTTCTTCTTCTTCTTCTT |
CCTTCTTCTTCTTCTTCTT |
15: 80,145,250 (GRCm39) |
|
probably benign |
Het |
Rsph4a |
T |
C |
10: 33,787,632 (GRCm39) |
I596T |
probably damaging |
Het |
Ryr2 |
A |
T |
13: 11,715,257 (GRCm39) |
Y2770* |
probably null |
Het |
Sctr |
T |
C |
1: 119,959,386 (GRCm39) |
F110L |
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 |
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 |
Sertad4 |
T |
C |
1: 192,529,340 (GRCm39) |
T159A |
probably benign |
Het |
Setd1a |
T |
A |
7: 127,384,296 (GRCm39) |
Y382* |
probably null |
Het |
Sfswap |
T |
A |
5: 129,590,304 (GRCm39) |
V267E |
possibly damaging |
Het |
Shank1 |
T |
A |
7: 44,002,161 (GRCm39) |
D1293E |
possibly damaging |
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 |
Slc36a1 |
A |
G |
11: 55,114,498 (GRCm39) |
D192G |
probably damaging |
Het |
Slc4a4 |
T |
A |
5: 89,280,273 (GRCm39) |
L366Q |
probably damaging |
Het |
Sorcs1 |
T |
C |
19: 50,216,747 (GRCm39) |
|
probably null |
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 |
Svep1 |
T |
A |
4: 58,073,333 (GRCm39) |
Y1992F |
probably benign |
Het |
Syce1l |
A |
G |
8: 114,381,466 (GRCm39) |
R152G |
possibly damaging |
Het |
Tbc1d17 |
A |
C |
7: 44,494,555 (GRCm39) |
S227A |
probably damaging |
Het |
Telo2 |
A |
T |
17: 25,321,712 (GRCm39) |
|
probably null |
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 |
Tmem143 |
G |
A |
7: 45,556,426 (GRCm39) |
D144N |
possibly damaging |
Het |
Tmprss11a |
T |
A |
5: 86,567,891 (GRCm39) |
I279F |
probably damaging |
Het |
Tnc |
A |
G |
4: 63,936,333 (GRCm39) |
L201P |
probably damaging |
Het |
Tnnt2 |
C |
T |
1: 135,773,244 (GRCm39) |
|
probably benign |
Het |
Ttn |
A |
G |
2: 76,619,245 (GRCm39) |
|
probably null |
Het |
Ttn |
C |
T |
2: 76,643,683 (GRCm39) |
G11436R |
probably damaging |
Het |
Ube2t |
C |
T |
1: 134,899,905 (GRCm39) |
A149V |
probably benign |
Het |
Unc80 |
G |
A |
1: 66,722,432 (GRCm39) |
M3015I |
probably benign |
Het |
Usp9y |
A |
T |
Y: 1,367,093 (GRCm39) |
V998D |
probably benign |
Het |
Utrn |
A |
G |
10: 12,339,083 (GRCm39) |
F2858S |
probably damaging |
Het |
Vmn1r224 |
T |
C |
17: 20,639,447 (GRCm39) |
I8T |
probably benign |
Het |
Vmn2r107 |
T |
C |
17: 20,576,775 (GRCm39) |
S258P |
possibly damaging |
Het |
Wars1 |
A |
C |
12: 108,841,667 (GRCm39) |
F160C |
probably damaging |
Het |
Xirp1 |
T |
G |
9: 120,016,907 (GRCm38) |
Q970P |
probably benign |
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 |
Zfp28 |
A |
T |
7: 6,397,791 (GRCm39) |
Y742F |
probably damaging |
Het |
Zfp541 |
A |
G |
7: 15,811,898 (GRCm39) |
T184A |
probably damaging |
Het |
Zfp623 |
T |
C |
15: 75,819,760 (GRCm39) |
S239P |
probably damaging |
Het |
Zfp804b |
T |
C |
5: 6,821,938 (GRCm39) |
D375G |
probably 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 Dock10 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00569:Dock10
|
APN |
1 |
80,562,729 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00783:Dock10
|
APN |
1 |
80,550,166 (GRCm39) |
splice site |
probably benign |
|
IGL00784:Dock10
|
APN |
1 |
80,550,166 (GRCm39) |
splice site |
probably benign |
|
IGL00858:Dock10
|
APN |
1 |
80,545,720 (GRCm39) |
missense |
possibly damaging |
0.48 |
IGL01298:Dock10
|
APN |
1 |
80,508,962 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01351:Dock10
|
APN |
1 |
80,570,876 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01356:Dock10
|
APN |
1 |
80,501,459 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01584:Dock10
|
APN |
1 |
80,511,567 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01619:Dock10
|
APN |
1 |
80,612,015 (GRCm39) |
splice site |
probably benign |
|
IGL01678:Dock10
|
APN |
1 |
80,521,069 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01759:Dock10
|
APN |
1 |
80,503,990 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02238:Dock10
|
APN |
1 |
80,511,510 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02352:Dock10
|
APN |
1 |
80,483,378 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02359:Dock10
|
APN |
1 |
80,483,378 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02377:Dock10
|
APN |
1 |
80,562,711 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02433:Dock10
|
APN |
1 |
80,507,905 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02471:Dock10
|
APN |
1 |
80,493,339 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02645:Dock10
|
APN |
1 |
80,551,840 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02646:Dock10
|
APN |
1 |
80,551,840 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02648:Dock10
|
APN |
1 |
80,551,840 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02649:Dock10
|
APN |
1 |
80,551,840 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02650:Dock10
|
APN |
1 |
80,551,840 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02652:Dock10
|
APN |
1 |
80,570,561 (GRCm39) |
splice site |
probably null |
|
IGL02718:Dock10
|
APN |
1 |
80,501,535 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02998:Dock10
|
APN |
1 |
80,551,259 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03057:Dock10
|
APN |
1 |
80,545,088 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03066:Dock10
|
APN |
1 |
80,562,758 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03106:Dock10
|
APN |
1 |
80,546,551 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03148:Dock10
|
APN |
1 |
80,518,075 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03271:Dock10
|
APN |
1 |
80,483,126 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03352:Dock10
|
APN |
1 |
80,584,013 (GRCm39) |
splice site |
probably benign |
|
LCD18:Dock10
|
UTSW |
1 |
80,716,623 (GRCm38) |
intron |
probably benign |
|
PIT4366001:Dock10
|
UTSW |
1 |
80,573,438 (GRCm39) |
missense |
probably benign |
0.30 |
PIT4581001:Dock10
|
UTSW |
1 |
80,483,163 (GRCm39) |
missense |
probably damaging |
1.00 |
R0019:Dock10
|
UTSW |
1 |
80,583,642 (GRCm39) |
missense |
probably damaging |
1.00 |
R0081:Dock10
|
UTSW |
1 |
80,584,295 (GRCm39) |
missense |
probably damaging |
0.99 |
R0095:Dock10
|
UTSW |
1 |
80,501,788 (GRCm39) |
missense |
probably benign |
0.00 |
R0241:Dock10
|
UTSW |
1 |
80,556,340 (GRCm39) |
missense |
probably benign |
|
R0241:Dock10
|
UTSW |
1 |
80,556,340 (GRCm39) |
missense |
probably benign |
|
R0255:Dock10
|
UTSW |
1 |
80,583,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R0267:Dock10
|
UTSW |
1 |
80,490,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R0299:Dock10
|
UTSW |
1 |
80,514,646 (GRCm39) |
missense |
probably damaging |
0.99 |
R0365:Dock10
|
UTSW |
1 |
80,573,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R0387:Dock10
|
UTSW |
1 |
80,517,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R0403:Dock10
|
UTSW |
1 |
80,501,787 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0408:Dock10
|
UTSW |
1 |
80,518,193 (GRCm39) |
missense |
probably benign |
0.03 |
R0414:Dock10
|
UTSW |
1 |
80,513,650 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0591:Dock10
|
UTSW |
1 |
80,518,936 (GRCm39) |
splice site |
probably benign |
|
R0698:Dock10
|
UTSW |
1 |
80,507,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R0711:Dock10
|
UTSW |
1 |
80,501,692 (GRCm39) |
missense |
probably damaging |
1.00 |
R0925:Dock10
|
UTSW |
1 |
80,514,657 (GRCm39) |
missense |
probably benign |
0.20 |
R1162:Dock10
|
UTSW |
1 |
80,546,559 (GRCm39) |
missense |
possibly damaging |
0.58 |
R1370:Dock10
|
UTSW |
1 |
80,518,060 (GRCm39) |
missense |
probably damaging |
1.00 |
R1440:Dock10
|
UTSW |
1 |
80,526,853 (GRCm39) |
missense |
probably benign |
0.03 |
R1469:Dock10
|
UTSW |
1 |
80,490,275 (GRCm39) |
missense |
probably benign |
0.05 |
R1469:Dock10
|
UTSW |
1 |
80,490,275 (GRCm39) |
missense |
probably benign |
0.05 |
R1525:Dock10
|
UTSW |
1 |
80,583,881 (GRCm39) |
critical splice donor site |
probably null |
|
R1544:Dock10
|
UTSW |
1 |
80,570,352 (GRCm39) |
missense |
probably benign |
0.00 |
R1601:Dock10
|
UTSW |
1 |
80,527,519 (GRCm39) |
missense |
probably benign |
0.00 |
R1757:Dock10
|
UTSW |
1 |
80,511,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R1765:Dock10
|
UTSW |
1 |
80,583,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R1823:Dock10
|
UTSW |
1 |
80,520,814 (GRCm39) |
splice site |
probably null |
|
R1827:Dock10
|
UTSW |
1 |
80,508,009 (GRCm39) |
missense |
probably benign |
0.07 |
R1844:Dock10
|
UTSW |
1 |
80,520,918 (GRCm39) |
missense |
probably damaging |
0.99 |
R1856:Dock10
|
UTSW |
1 |
80,584,285 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1974:Dock10
|
UTSW |
1 |
80,488,143 (GRCm39) |
missense |
possibly damaging |
0.50 |
R2006:Dock10
|
UTSW |
1 |
80,527,506 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2112:Dock10
|
UTSW |
1 |
80,483,360 (GRCm39) |
missense |
probably damaging |
0.99 |
R2112:Dock10
|
UTSW |
1 |
80,483,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R2113:Dock10
|
UTSW |
1 |
80,584,280 (GRCm39) |
missense |
probably damaging |
1.00 |
R2439:Dock10
|
UTSW |
1 |
80,510,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R2566:Dock10
|
UTSW |
1 |
80,517,970 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3086:Dock10
|
UTSW |
1 |
80,510,074 (GRCm39) |
missense |
possibly damaging |
0.91 |
R3766:Dock10
|
UTSW |
1 |
80,514,643 (GRCm39) |
missense |
probably damaging |
0.99 |
R3768:Dock10
|
UTSW |
1 |
80,510,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R4009:Dock10
|
UTSW |
1 |
80,510,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R4016:Dock10
|
UTSW |
1 |
80,584,286 (GRCm39) |
missense |
probably damaging |
1.00 |
R4179:Dock10
|
UTSW |
1 |
80,488,134 (GRCm39) |
missense |
probably benign |
0.00 |
R4243:Dock10
|
UTSW |
1 |
80,544,472 (GRCm39) |
missense |
probably benign |
0.00 |
R4244:Dock10
|
UTSW |
1 |
80,544,472 (GRCm39) |
missense |
probably benign |
0.00 |
R4245:Dock10
|
UTSW |
1 |
80,544,472 (GRCm39) |
missense |
probably benign |
0.00 |
R4674:Dock10
|
UTSW |
1 |
80,584,337 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4696:Dock10
|
UTSW |
1 |
80,493,330 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4789:Dock10
|
UTSW |
1 |
80,518,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R4851:Dock10
|
UTSW |
1 |
80,526,874 (GRCm39) |
missense |
probably benign |
0.33 |
R4911:Dock10
|
UTSW |
1 |
80,583,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R4976:Dock10
|
UTSW |
1 |
80,545,711 (GRCm39) |
critical splice donor site |
probably null |
|
R5086:Dock10
|
UTSW |
1 |
80,529,189 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5119:Dock10
|
UTSW |
1 |
80,545,711 (GRCm39) |
critical splice donor site |
probably null |
|
R5301:Dock10
|
UTSW |
1 |
80,625,973 (GRCm39) |
missense |
probably benign |
0.41 |
R5404:Dock10
|
UTSW |
1 |
80,481,630 (GRCm39) |
intron |
probably benign |
|
R5457:Dock10
|
UTSW |
1 |
80,501,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R5790:Dock10
|
UTSW |
1 |
80,482,887 (GRCm39) |
missense |
probably benign |
0.00 |
R5845:Dock10
|
UTSW |
1 |
80,483,459 (GRCm39) |
intron |
probably benign |
|
R5871:Dock10
|
UTSW |
1 |
80,519,057 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5873:Dock10
|
UTSW |
1 |
80,551,855 (GRCm39) |
missense |
probably damaging |
1.00 |
R5881:Dock10
|
UTSW |
1 |
80,538,640 (GRCm39) |
missense |
probably benign |
0.19 |
R5895:Dock10
|
UTSW |
1 |
80,514,676 (GRCm39) |
missense |
probably benign |
|
R5935:Dock10
|
UTSW |
1 |
80,483,304 (GRCm39) |
intron |
probably benign |
|
R5965:Dock10
|
UTSW |
1 |
80,546,461 (GRCm39) |
splice site |
probably null |
|
R5966:Dock10
|
UTSW |
1 |
80,546,225 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6008:Dock10
|
UTSW |
1 |
80,583,890 (GRCm39) |
missense |
probably damaging |
0.98 |
R6029:Dock10
|
UTSW |
1 |
80,514,663 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6083:Dock10
|
UTSW |
1 |
80,510,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R6145:Dock10
|
UTSW |
1 |
80,553,621 (GRCm39) |
nonsense |
probably null |
|
R6257:Dock10
|
UTSW |
1 |
80,481,413 (GRCm39) |
intron |
probably benign |
|
R6274:Dock10
|
UTSW |
1 |
80,516,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R6324:Dock10
|
UTSW |
1 |
80,482,893 (GRCm39) |
missense |
probably benign |
0.03 |
R6346:Dock10
|
UTSW |
1 |
80,553,573 (GRCm39) |
splice site |
probably null |
|
R6476:Dock10
|
UTSW |
1 |
80,518,959 (GRCm39) |
nonsense |
probably null |
|
R6516:Dock10
|
UTSW |
1 |
80,518,178 (GRCm39) |
missense |
probably damaging |
1.00 |
R6526:Dock10
|
UTSW |
1 |
80,564,068 (GRCm39) |
missense |
probably damaging |
0.97 |
R6534:Dock10
|
UTSW |
1 |
80,481,388 (GRCm39) |
missense |
probably benign |
0.01 |
R6620:Dock10
|
UTSW |
1 |
80,570,355 (GRCm39) |
missense |
probably benign |
0.01 |
R6640:Dock10
|
UTSW |
1 |
80,511,555 (GRCm39) |
nonsense |
probably null |
|
R6669:Dock10
|
UTSW |
1 |
80,570,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R6672:Dock10
|
UTSW |
1 |
80,490,248 (GRCm39) |
missense |
probably benign |
0.00 |
R6679:Dock10
|
UTSW |
1 |
80,544,514 (GRCm39) |
missense |
probably benign |
0.11 |
R6682:Dock10
|
UTSW |
1 |
80,490,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R6712:Dock10
|
UTSW |
1 |
80,514,583 (GRCm39) |
missense |
probably benign |
0.00 |
R6726:Dock10
|
UTSW |
1 |
80,490,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R6788:Dock10
|
UTSW |
1 |
80,508,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R6805:Dock10
|
UTSW |
1 |
80,564,407 (GRCm39) |
missense |
probably benign |
|
R6815:Dock10
|
UTSW |
1 |
80,516,576 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6818:Dock10
|
UTSW |
1 |
80,593,082 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6867:Dock10
|
UTSW |
1 |
80,508,976 (GRCm39) |
missense |
probably damaging |
1.00 |
R6964:Dock10
|
UTSW |
1 |
80,481,365 (GRCm39) |
intron |
probably benign |
|
R7026:Dock10
|
UTSW |
1 |
80,479,504 (GRCm39) |
missense |
probably benign |
0.40 |
R7084:Dock10
|
UTSW |
1 |
80,481,573 (GRCm39) |
missense |
|
|
R7087:Dock10
|
UTSW |
1 |
80,570,543 (GRCm39) |
missense |
probably benign |
|
R7158:Dock10
|
UTSW |
1 |
80,564,589 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7191:Dock10
|
UTSW |
1 |
80,518,048 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7214:Dock10
|
UTSW |
1 |
80,546,246 (GRCm39) |
missense |
probably benign |
0.01 |
R7255:Dock10
|
UTSW |
1 |
80,520,816 (GRCm39) |
critical splice donor site |
probably null |
|
R7320:Dock10
|
UTSW |
1 |
80,527,421 (GRCm39) |
critical splice donor site |
probably null |
|
R7359:Dock10
|
UTSW |
1 |
80,687,065 (GRCm39) |
missense |
probably benign |
0.01 |
R7423:Dock10
|
UTSW |
1 |
80,501,497 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7464:Dock10
|
UTSW |
1 |
80,518,032 (GRCm39) |
missense |
probably damaging |
0.99 |
R7483:Dock10
|
UTSW |
1 |
80,493,283 (GRCm39) |
missense |
probably benign |
0.01 |
R7487:Dock10
|
UTSW |
1 |
80,562,765 (GRCm39) |
missense |
probably benign |
0.00 |
R7789:Dock10
|
UTSW |
1 |
80,536,930 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7943:Dock10
|
UTSW |
1 |
80,626,006 (GRCm39) |
missense |
probably damaging |
0.98 |
R7962:Dock10
|
UTSW |
1 |
80,564,085 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8079:Dock10
|
UTSW |
1 |
80,556,421 (GRCm39) |
missense |
probably benign |
0.00 |
R8086:Dock10
|
UTSW |
1 |
80,481,707 (GRCm39) |
missense |
probably benign |
0.17 |
R8184:Dock10
|
UTSW |
1 |
80,530,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R8220:Dock10
|
UTSW |
1 |
80,506,366 (GRCm39) |
missense |
probably null |
1.00 |
R8225:Dock10
|
UTSW |
1 |
80,481,447 (GRCm39) |
nonsense |
probably null |
|
R8267:Dock10
|
UTSW |
1 |
80,518,045 (GRCm39) |
missense |
probably benign |
0.00 |
R8276:Dock10
|
UTSW |
1 |
80,505,998 (GRCm39) |
missense |
probably benign |
|
R8294:Dock10
|
UTSW |
1 |
80,488,079 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8298:Dock10
|
UTSW |
1 |
80,514,654 (GRCm39) |
missense |
probably benign |
0.00 |
R8326:Dock10
|
UTSW |
1 |
80,583,892 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8724:Dock10
|
UTSW |
1 |
80,570,344 (GRCm39) |
missense |
probably benign |
0.00 |
R8828:Dock10
|
UTSW |
1 |
80,521,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R8846:Dock10
|
UTSW |
1 |
80,545,786 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8919:Dock10
|
UTSW |
1 |
80,483,147 (GRCm39) |
missense |
probably benign |
0.00 |
R8950:Dock10
|
UTSW |
1 |
80,519,016 (GRCm39) |
missense |
probably benign |
|
R8993:Dock10
|
UTSW |
1 |
80,551,888 (GRCm39) |
missense |
probably benign |
0.21 |
R9028:Dock10
|
UTSW |
1 |
80,584,012 (GRCm39) |
splice site |
probably benign |
|
R9115:Dock10
|
UTSW |
1 |
80,490,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R9327:Dock10
|
UTSW |
1 |
80,510,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R9342:Dock10
|
UTSW |
1 |
80,570,360 (GRCm39) |
missense |
probably benign |
|
R9421:Dock10
|
UTSW |
1 |
80,501,509 (GRCm39) |
missense |
probably damaging |
1.00 |
R9431:Dock10
|
UTSW |
1 |
80,583,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R9486:Dock10
|
UTSW |
1 |
80,479,452 (GRCm39) |
missense |
unknown |
|
R9521:Dock10
|
UTSW |
1 |
80,501,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R9598:Dock10
|
UTSW |
1 |
80,625,939 (GRCm39) |
missense |
probably benign |
0.15 |
R9629:Dock10
|
UTSW |
1 |
80,481,389 (GRCm39) |
missense |
|
|
R9703:Dock10
|
UTSW |
1 |
80,517,540 (GRCm39) |
missense |
probably damaging |
0.98 |
RF021:Dock10
|
UTSW |
1 |
80,542,290 (GRCm39) |
critical splice acceptor site |
probably null |
|
X0025:Dock10
|
UTSW |
1 |
80,514,637 (GRCm39) |
missense |
probably damaging |
0.98 |
X0065:Dock10
|
UTSW |
1 |
80,518,977 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Dock10
|
UTSW |
1 |
80,510,064 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Dock10
|
UTSW |
1 |
80,538,671 (GRCm39) |
missense |
probably benign |
|
Z1177:Dock10
|
UTSW |
1 |
80,536,917 (GRCm39) |
missense |
probably benign |
0.04 |
|