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 |
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 |
A |
1: 107,451,564 (GRCm39) |
A239E |
probably benign |
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 |
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 |
Zfyve26 |
T |
A |
12: 79,315,208 (GRCm39) |
I1423F |
possibly damaging |
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 Dnah5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00226:Dnah5
|
APN |
15 |
28,272,488 (GRCm39) |
missense |
probably benign |
|
IGL00331:Dnah5
|
APN |
15 |
28,421,766 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00519:Dnah5
|
APN |
15 |
28,444,364 (GRCm39) |
missense |
probably benign |
0.10 |
IGL00537:Dnah5
|
APN |
15 |
28,458,848 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01102:Dnah5
|
APN |
15 |
28,410,149 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01126:Dnah5
|
APN |
15 |
28,302,545 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL01154:Dnah5
|
APN |
15 |
28,458,802 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL01349:Dnah5
|
APN |
15 |
28,295,059 (GRCm39) |
splice site |
probably benign |
|
IGL01353:Dnah5
|
APN |
15 |
28,233,418 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01372:Dnah5
|
APN |
15 |
28,230,636 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01390:Dnah5
|
APN |
15 |
28,411,686 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01446:Dnah5
|
APN |
15 |
28,326,815 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01472:Dnah5
|
APN |
15 |
28,331,872 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01485:Dnah5
|
APN |
15 |
28,331,872 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01568:Dnah5
|
APN |
15 |
28,229,798 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01592:Dnah5
|
APN |
15 |
28,236,783 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01594:Dnah5
|
APN |
15 |
28,311,480 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL01677:Dnah5
|
APN |
15 |
28,367,928 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01845:Dnah5
|
APN |
15 |
28,449,315 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01904:Dnah5
|
APN |
15 |
28,307,510 (GRCm39) |
missense |
probably benign |
0.09 |
IGL01913:Dnah5
|
APN |
15 |
28,313,899 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL01950:Dnah5
|
APN |
15 |
28,290,435 (GRCm39) |
missense |
probably null |
1.00 |
IGL01963:Dnah5
|
APN |
15 |
28,370,682 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02008:Dnah5
|
APN |
15 |
28,343,698 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02088:Dnah5
|
APN |
15 |
28,459,264 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02090:Dnah5
|
APN |
15 |
28,240,187 (GRCm39) |
splice site |
probably benign |
|
IGL02114:Dnah5
|
APN |
15 |
28,397,270 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02135:Dnah5
|
APN |
15 |
28,248,031 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL02232:Dnah5
|
APN |
15 |
28,299,386 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02386:Dnah5
|
APN |
15 |
28,340,527 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02475:Dnah5
|
APN |
15 |
28,219,296 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02626:Dnah5
|
APN |
15 |
28,307,422 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02650:Dnah5
|
APN |
15 |
28,289,193 (GRCm39) |
splice site |
probably benign |
|
IGL02651:Dnah5
|
APN |
15 |
28,350,768 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02652:Dnah5
|
APN |
15 |
28,366,333 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02670:Dnah5
|
APN |
15 |
28,409,442 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02697:Dnah5
|
APN |
15 |
28,445,289 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02721:Dnah5
|
APN |
15 |
28,234,389 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02858:Dnah5
|
APN |
15 |
28,453,358 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL02859:Dnah5
|
APN |
15 |
28,383,771 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02945:Dnah5
|
APN |
15 |
28,270,572 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02949:Dnah5
|
APN |
15 |
28,272,331 (GRCm39) |
missense |
probably benign |
0.32 |
IGL02971:Dnah5
|
APN |
15 |
28,384,607 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03017:Dnah5
|
APN |
15 |
28,340,471 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL03177:Dnah5
|
APN |
15 |
28,295,545 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03212:Dnah5
|
APN |
15 |
28,290,309 (GRCm39) |
missense |
probably benign |
0.08 |
IGL03224:Dnah5
|
APN |
15 |
28,459,300 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03231:Dnah5
|
APN |
15 |
28,311,294 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03273:Dnah5
|
APN |
15 |
28,458,795 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03294:Dnah5
|
APN |
15 |
28,233,441 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03331:Dnah5
|
APN |
15 |
28,420,086 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03337:Dnah5
|
APN |
15 |
28,290,287 (GRCm39) |
missense |
probably benign |
0.10 |
IGL03367:Dnah5
|
APN |
15 |
28,234,473 (GRCm39) |
missense |
possibly damaging |
0.95 |
Firtel
|
UTSW |
15 |
28,448,513 (GRCm39) |
missense |
possibly damaging |
0.95 |
lowbar
|
UTSW |
15 |
28,311,279 (GRCm39) |
splice site |
probably null |
|
notherone
|
UTSW |
15 |
28,340,552 (GRCm39) |
missense |
probably benign |
0.13 |
scheffler
|
UTSW |
15 |
28,438,237 (GRCm39) |
splice site |
probably benign |
|
IGL02837:Dnah5
|
UTSW |
15 |
28,269,546 (GRCm39) |
missense |
probably benign |
|
P0008:Dnah5
|
UTSW |
15 |
28,302,533 (GRCm39) |
missense |
probably damaging |
1.00 |
P0014:Dnah5
|
UTSW |
15 |
28,403,619 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4687001:Dnah5
|
UTSW |
15 |
28,383,723 (GRCm39) |
missense |
probably damaging |
0.98 |
R0030:Dnah5
|
UTSW |
15 |
28,451,663 (GRCm39) |
missense |
probably benign |
0.34 |
R0087:Dnah5
|
UTSW |
15 |
28,350,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R0099:Dnah5
|
UTSW |
15 |
28,240,080 (GRCm39) |
missense |
probably damaging |
1.00 |
R0102:Dnah5
|
UTSW |
15 |
28,245,897 (GRCm39) |
splice site |
probably benign |
|
R0102:Dnah5
|
UTSW |
15 |
28,245,897 (GRCm39) |
splice site |
probably benign |
|
R0104:Dnah5
|
UTSW |
15 |
28,453,499 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0112:Dnah5
|
UTSW |
15 |
28,263,825 (GRCm39) |
missense |
probably benign |
0.00 |
R0122:Dnah5
|
UTSW |
15 |
28,378,509 (GRCm39) |
missense |
probably damaging |
1.00 |
R0126:Dnah5
|
UTSW |
15 |
28,246,465 (GRCm39) |
missense |
probably benign |
0.00 |
R0127:Dnah5
|
UTSW |
15 |
28,295,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R0233:Dnah5
|
UTSW |
15 |
28,333,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R0310:Dnah5
|
UTSW |
15 |
28,299,256 (GRCm39) |
missense |
probably benign |
0.19 |
R0386:Dnah5
|
UTSW |
15 |
28,383,727 (GRCm39) |
missense |
probably damaging |
1.00 |
R0421:Dnah5
|
UTSW |
15 |
28,229,687 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0481:Dnah5
|
UTSW |
15 |
28,383,745 (GRCm39) |
missense |
probably benign |
0.31 |
R0514:Dnah5
|
UTSW |
15 |
28,366,467 (GRCm39) |
missense |
probably damaging |
1.00 |
R0609:Dnah5
|
UTSW |
15 |
28,327,925 (GRCm39) |
missense |
probably benign |
|
R0720:Dnah5
|
UTSW |
15 |
28,314,007 (GRCm39) |
missense |
probably null |
0.98 |
R0731:Dnah5
|
UTSW |
15 |
28,311,289 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0747:Dnah5
|
UTSW |
15 |
28,444,333 (GRCm39) |
missense |
possibly damaging |
0.64 |
R0747:Dnah5
|
UTSW |
15 |
28,444,332 (GRCm39) |
missense |
probably damaging |
0.99 |
R0766:Dnah5
|
UTSW |
15 |
28,448,633 (GRCm39) |
missense |
probably null |
0.89 |
R0849:Dnah5
|
UTSW |
15 |
28,263,745 (GRCm39) |
missense |
probably damaging |
0.96 |
R1034:Dnah5
|
UTSW |
15 |
28,302,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R1084:Dnah5
|
UTSW |
15 |
28,343,598 (GRCm39) |
missense |
probably benign |
0.01 |
R1148:Dnah5
|
UTSW |
15 |
28,421,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R1148:Dnah5
|
UTSW |
15 |
28,421,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R1200:Dnah5
|
UTSW |
15 |
28,246,403 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1208:Dnah5
|
UTSW |
15 |
28,327,877 (GRCm39) |
missense |
probably damaging |
1.00 |
R1208:Dnah5
|
UTSW |
15 |
28,327,877 (GRCm39) |
missense |
probably damaging |
1.00 |
R1269:Dnah5
|
UTSW |
15 |
28,238,657 (GRCm39) |
missense |
probably damaging |
1.00 |
R1373:Dnah5
|
UTSW |
15 |
28,314,064 (GRCm39) |
splice site |
probably benign |
|
R1401:Dnah5
|
UTSW |
15 |
28,402,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R1413:Dnah5
|
UTSW |
15 |
28,370,555 (GRCm39) |
missense |
probably benign |
|
R1430:Dnah5
|
UTSW |
15 |
28,346,003 (GRCm39) |
missense |
probably benign |
0.37 |
R1457:Dnah5
|
UTSW |
15 |
28,403,688 (GRCm39) |
critical splice donor site |
probably null |
|
R1468:Dnah5
|
UTSW |
15 |
28,230,609 (GRCm39) |
nonsense |
probably null |
|
R1468:Dnah5
|
UTSW |
15 |
28,230,609 (GRCm39) |
nonsense |
probably null |
|
R1560:Dnah5
|
UTSW |
15 |
28,420,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R1568:Dnah5
|
UTSW |
15 |
28,409,323 (GRCm39) |
missense |
probably damaging |
0.98 |
R1574:Dnah5
|
UTSW |
15 |
28,252,569 (GRCm39) |
missense |
probably benign |
0.00 |
R1574:Dnah5
|
UTSW |
15 |
28,252,569 (GRCm39) |
missense |
probably benign |
0.00 |
R1603:Dnah5
|
UTSW |
15 |
28,449,326 (GRCm39) |
missense |
probably benign |
0.09 |
R1603:Dnah5
|
UTSW |
15 |
28,295,131 (GRCm39) |
splice site |
probably benign |
|
R1673:Dnah5
|
UTSW |
15 |
28,290,294 (GRCm39) |
missense |
probably benign |
|
R1755:Dnah5
|
UTSW |
15 |
28,326,782 (GRCm39) |
missense |
probably damaging |
0.99 |
R1786:Dnah5
|
UTSW |
15 |
28,313,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R1789:Dnah5
|
UTSW |
15 |
28,270,572 (GRCm39) |
missense |
probably benign |
0.00 |
R1817:Dnah5
|
UTSW |
15 |
28,246,546 (GRCm39) |
nonsense |
probably null |
|
R1819:Dnah5
|
UTSW |
15 |
28,246,546 (GRCm39) |
nonsense |
probably null |
|
R1834:Dnah5
|
UTSW |
15 |
28,409,270 (GRCm39) |
missense |
probably benign |
0.00 |
R1855:Dnah5
|
UTSW |
15 |
28,411,815 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1870:Dnah5
|
UTSW |
15 |
28,331,859 (GRCm39) |
nonsense |
probably null |
|
R1871:Dnah5
|
UTSW |
15 |
28,331,859 (GRCm39) |
nonsense |
probably null |
|
R1987:Dnah5
|
UTSW |
15 |
28,343,737 (GRCm39) |
missense |
probably damaging |
0.99 |
R1988:Dnah5
|
UTSW |
15 |
28,343,737 (GRCm39) |
missense |
probably damaging |
0.99 |
R1989:Dnah5
|
UTSW |
15 |
28,343,737 (GRCm39) |
missense |
probably damaging |
0.99 |
R2062:Dnah5
|
UTSW |
15 |
28,366,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R2069:Dnah5
|
UTSW |
15 |
28,312,534 (GRCm39) |
splice site |
probably null |
|
R2121:Dnah5
|
UTSW |
15 |
28,297,151 (GRCm39) |
splice site |
probably benign |
|
R2128:Dnah5
|
UTSW |
15 |
28,408,467 (GRCm39) |
missense |
probably benign |
0.00 |
R2129:Dnah5
|
UTSW |
15 |
28,408,467 (GRCm39) |
missense |
probably benign |
0.00 |
R2151:Dnah5
|
UTSW |
15 |
28,444,237 (GRCm39) |
missense |
probably damaging |
1.00 |
R2159:Dnah5
|
UTSW |
15 |
28,252,691 (GRCm39) |
missense |
probably benign |
0.00 |
R2207:Dnah5
|
UTSW |
15 |
28,343,817 (GRCm39) |
missense |
probably benign |
0.11 |
R2231:Dnah5
|
UTSW |
15 |
28,408,563 (GRCm39) |
critical splice donor site |
probably null |
|
R2232:Dnah5
|
UTSW |
15 |
28,408,563 (GRCm39) |
critical splice donor site |
probably null |
|
R2282:Dnah5
|
UTSW |
15 |
28,327,448 (GRCm39) |
missense |
probably damaging |
0.99 |
R2305:Dnah5
|
UTSW |
15 |
28,387,913 (GRCm39) |
missense |
probably benign |
0.25 |
R2339:Dnah5
|
UTSW |
15 |
28,314,028 (GRCm39) |
missense |
probably benign |
0.00 |
R2437:Dnah5
|
UTSW |
15 |
28,307,537 (GRCm39) |
critical splice donor site |
probably null |
|
R2696:Dnah5
|
UTSW |
15 |
28,278,722 (GRCm39) |
missense |
probably benign |
0.00 |
R3156:Dnah5
|
UTSW |
15 |
28,438,237 (GRCm39) |
splice site |
probably benign |
|
R3431:Dnah5
|
UTSW |
15 |
28,295,413 (GRCm39) |
missense |
probably benign |
0.20 |
R3700:Dnah5
|
UTSW |
15 |
28,387,937 (GRCm39) |
missense |
possibly damaging |
0.72 |
R3724:Dnah5
|
UTSW |
15 |
28,270,566 (GRCm39) |
missense |
probably benign |
0.08 |
R3732:Dnah5
|
UTSW |
15 |
28,409,268 (GRCm39) |
missense |
possibly damaging |
0.64 |
R3872:Dnah5
|
UTSW |
15 |
28,411,656 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4063:Dnah5
|
UTSW |
15 |
28,421,144 (GRCm39) |
missense |
probably damaging |
0.98 |
R4072:Dnah5
|
UTSW |
15 |
28,340,444 (GRCm39) |
nonsense |
probably null |
|
R4075:Dnah5
|
UTSW |
15 |
28,293,937 (GRCm39) |
missense |
probably benign |
|
R4245:Dnah5
|
UTSW |
15 |
28,219,335 (GRCm39) |
missense |
probably benign |
|
R4254:Dnah5
|
UTSW |
15 |
28,438,248 (GRCm39) |
missense |
probably benign |
0.07 |
R4255:Dnah5
|
UTSW |
15 |
28,438,248 (GRCm39) |
missense |
probably benign |
0.07 |
R4392:Dnah5
|
UTSW |
15 |
28,289,375 (GRCm39) |
missense |
probably benign |
0.19 |
R4552:Dnah5
|
UTSW |
15 |
28,397,300 (GRCm39) |
missense |
probably benign |
0.19 |
R4574:Dnah5
|
UTSW |
15 |
28,367,909 (GRCm39) |
missense |
probably benign |
0.05 |
R4577:Dnah5
|
UTSW |
15 |
28,289,396 (GRCm39) |
missense |
probably benign |
0.06 |
R4587:Dnah5
|
UTSW |
15 |
28,304,745 (GRCm39) |
missense |
probably damaging |
1.00 |
R4631:Dnah5
|
UTSW |
15 |
28,420,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R4631:Dnah5
|
UTSW |
15 |
28,402,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R4676:Dnah5
|
UTSW |
15 |
28,295,406 (GRCm39) |
missense |
possibly damaging |
0.65 |
R4707:Dnah5
|
UTSW |
15 |
28,372,521 (GRCm39) |
missense |
probably damaging |
0.97 |
R4754:Dnah5
|
UTSW |
15 |
28,421,101 (GRCm39) |
splice site |
probably null |
|
R4767:Dnah5
|
UTSW |
15 |
28,270,620 (GRCm39) |
missense |
probably benign |
0.02 |
R4857:Dnah5
|
UTSW |
15 |
28,345,953 (GRCm39) |
missense |
probably benign |
0.00 |
R4883:Dnah5
|
UTSW |
15 |
28,343,784 (GRCm39) |
missense |
probably benign |
0.00 |
R4889:Dnah5
|
UTSW |
15 |
28,235,938 (GRCm39) |
missense |
probably benign |
0.01 |
R4946:Dnah5
|
UTSW |
15 |
28,388,050 (GRCm39) |
missense |
probably damaging |
1.00 |
R4946:Dnah5
|
UTSW |
15 |
28,326,703 (GRCm39) |
missense |
probably damaging |
0.96 |
R4947:Dnah5
|
UTSW |
15 |
28,272,518 (GRCm39) |
missense |
probably benign |
|
R5033:Dnah5
|
UTSW |
15 |
28,421,824 (GRCm39) |
missense |
probably damaging |
0.96 |
R5164:Dnah5
|
UTSW |
15 |
28,408,438 (GRCm39) |
missense |
probably benign |
0.00 |
R5175:Dnah5
|
UTSW |
15 |
28,448,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R5182:Dnah5
|
UTSW |
15 |
28,311,424 (GRCm39) |
missense |
probably damaging |
0.99 |
R5187:Dnah5
|
UTSW |
15 |
28,272,318 (GRCm39) |
missense |
probably benign |
0.41 |
R5272:Dnah5
|
UTSW |
15 |
28,350,811 (GRCm39) |
missense |
probably benign |
|
R5308:Dnah5
|
UTSW |
15 |
28,229,797 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5310:Dnah5
|
UTSW |
15 |
28,311,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R5322:Dnah5
|
UTSW |
15 |
28,384,390 (GRCm39) |
missense |
probably benign |
0.41 |
R5398:Dnah5
|
UTSW |
15 |
28,293,872 (GRCm39) |
missense |
probably benign |
|
R5596:Dnah5
|
UTSW |
15 |
28,343,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R5603:Dnah5
|
UTSW |
15 |
28,420,078 (GRCm39) |
missense |
probably damaging |
1.00 |
R5619:Dnah5
|
UTSW |
15 |
28,302,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R5656:Dnah5
|
UTSW |
15 |
28,421,210 (GRCm39) |
missense |
probably benign |
0.03 |
R5741:Dnah5
|
UTSW |
15 |
28,246,513 (GRCm39) |
missense |
probably benign |
0.11 |
R5754:Dnah5
|
UTSW |
15 |
28,402,014 (GRCm39) |
missense |
probably benign |
0.01 |
R5763:Dnah5
|
UTSW |
15 |
28,311,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R5824:Dnah5
|
UTSW |
15 |
28,313,967 (GRCm39) |
missense |
probably benign |
0.00 |
R5836:Dnah5
|
UTSW |
15 |
28,383,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R5838:Dnah5
|
UTSW |
15 |
28,290,341 (GRCm39) |
missense |
probably benign |
0.00 |
R5864:Dnah5
|
UTSW |
15 |
28,297,159 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5895:Dnah5
|
UTSW |
15 |
28,234,599 (GRCm39) |
splice site |
probably null |
|
R5896:Dnah5
|
UTSW |
15 |
28,272,206 (GRCm39) |
missense |
probably benign |
|
R5899:Dnah5
|
UTSW |
15 |
28,448,513 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5905:Dnah5
|
UTSW |
15 |
28,387,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R5924:Dnah5
|
UTSW |
15 |
28,307,473 (GRCm39) |
missense |
probably benign |
0.41 |
R5927:Dnah5
|
UTSW |
15 |
28,335,864 (GRCm39) |
missense |
probably benign |
0.00 |
R5929:Dnah5
|
UTSW |
15 |
28,311,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R5929:Dnah5
|
UTSW |
15 |
28,311,353 (GRCm39) |
missense |
probably benign |
0.01 |
R5931:Dnah5
|
UTSW |
15 |
28,453,425 (GRCm39) |
missense |
probably damaging |
0.99 |
R5964:Dnah5
|
UTSW |
15 |
28,458,730 (GRCm39) |
missense |
possibly damaging |
0.49 |
R5975:Dnah5
|
UTSW |
15 |
28,234,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R5993:Dnah5
|
UTSW |
15 |
28,299,372 (GRCm39) |
missense |
probably benign |
0.09 |
R6016:Dnah5
|
UTSW |
15 |
28,328,030 (GRCm39) |
missense |
probably damaging |
1.00 |
R6028:Dnah5
|
UTSW |
15 |
28,387,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R6065:Dnah5
|
UTSW |
15 |
28,230,614 (GRCm39) |
missense |
possibly damaging |
0.47 |
R6117:Dnah5
|
UTSW |
15 |
28,270,566 (GRCm39) |
missense |
probably damaging |
0.99 |
R6143:Dnah5
|
UTSW |
15 |
28,233,377 (GRCm39) |
missense |
probably benign |
0.05 |
R6146:Dnah5
|
UTSW |
15 |
28,459,331 (GRCm39) |
missense |
probably benign |
|
R6154:Dnah5
|
UTSW |
15 |
28,204,177 (GRCm39) |
missense |
probably benign |
0.15 |
R6164:Dnah5
|
UTSW |
15 |
28,378,489 (GRCm39) |
missense |
probably benign |
0.08 |
R6266:Dnah5
|
UTSW |
15 |
28,335,773 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6321:Dnah5
|
UTSW |
15 |
28,372,557 (GRCm39) |
missense |
probably damaging |
0.99 |
R6349:Dnah5
|
UTSW |
15 |
28,238,657 (GRCm39) |
missense |
probably damaging |
1.00 |
R6431:Dnah5
|
UTSW |
15 |
28,349,970 (GRCm39) |
missense |
possibly damaging |
0.52 |
R6467:Dnah5
|
UTSW |
15 |
28,438,329 (GRCm39) |
missense |
probably benign |
0.10 |
R6564:Dnah5
|
UTSW |
15 |
28,367,891 (GRCm39) |
missense |
probably benign |
|
R6607:Dnah5
|
UTSW |
15 |
28,445,346 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6619:Dnah5
|
UTSW |
15 |
28,409,266 (GRCm39) |
missense |
probably benign |
0.03 |
R6633:Dnah5
|
UTSW |
15 |
28,293,933 (GRCm39) |
missense |
probably benign |
0.27 |
R6647:Dnah5
|
UTSW |
15 |
28,403,633 (GRCm39) |
missense |
probably benign |
0.02 |
R6782:Dnah5
|
UTSW |
15 |
28,449,302 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6797:Dnah5
|
UTSW |
15 |
28,233,384 (GRCm39) |
nonsense |
probably null |
|
R6797:Dnah5
|
UTSW |
15 |
28,451,609 (GRCm39) |
missense |
probably damaging |
1.00 |
R6831:Dnah5
|
UTSW |
15 |
28,411,661 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6849:Dnah5
|
UTSW |
15 |
28,278,770 (GRCm39) |
missense |
probably benign |
0.14 |
R6871:Dnah5
|
UTSW |
15 |
28,229,786 (GRCm39) |
missense |
probably benign |
0.32 |
R6936:Dnah5
|
UTSW |
15 |
28,409,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R6943:Dnah5
|
UTSW |
15 |
28,235,866 (GRCm39) |
missense |
probably damaging |
1.00 |
R7030:Dnah5
|
UTSW |
15 |
28,333,208 (GRCm39) |
missense |
probably benign |
0.00 |
R7030:Dnah5
|
UTSW |
15 |
28,238,738 (GRCm39) |
missense |
probably benign |
|
R7032:Dnah5
|
UTSW |
15 |
28,326,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R7063:Dnah5
|
UTSW |
15 |
28,233,394 (GRCm39) |
missense |
probably benign |
0.00 |
R7094:Dnah5
|
UTSW |
15 |
28,453,482 (GRCm39) |
missense |
probably damaging |
0.98 |
R7097:Dnah5
|
UTSW |
15 |
28,453,410 (GRCm39) |
missense |
probably benign |
0.00 |
R7126:Dnah5
|
UTSW |
15 |
28,349,983 (GRCm39) |
missense |
probably benign |
0.03 |
R7153:Dnah5
|
UTSW |
15 |
28,365,668 (GRCm39) |
splice site |
probably null |
|
R7209:Dnah5
|
UTSW |
15 |
28,459,371 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7276:Dnah5
|
UTSW |
15 |
28,367,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R7320:Dnah5
|
UTSW |
15 |
28,270,616 (GRCm39) |
missense |
probably null |
0.33 |
R7350:Dnah5
|
UTSW |
15 |
28,235,965 (GRCm39) |
critical splice donor site |
probably null |
|
R7380:Dnah5
|
UTSW |
15 |
28,370,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R7438:Dnah5
|
UTSW |
15 |
28,347,098 (GRCm39) |
missense |
probably damaging |
0.99 |
R7499:Dnah5
|
UTSW |
15 |
28,302,596 (GRCm39) |
missense |
probably damaging |
1.00 |
R7513:Dnah5
|
UTSW |
15 |
28,370,561 (GRCm39) |
missense |
probably benign |
|
R7519:Dnah5
|
UTSW |
15 |
28,390,629 (GRCm39) |
missense |
probably damaging |
0.98 |
R7524:Dnah5
|
UTSW |
15 |
28,297,212 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7556:Dnah5
|
UTSW |
15 |
28,290,389 (GRCm39) |
missense |
probably null |
0.43 |
R7570:Dnah5
|
UTSW |
15 |
28,347,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R7585:Dnah5
|
UTSW |
15 |
28,402,014 (GRCm39) |
missense |
probably benign |
0.09 |
R7642:Dnah5
|
UTSW |
15 |
28,248,125 (GRCm39) |
critical splice donor site |
probably null |
|
R7670:Dnah5
|
UTSW |
15 |
28,246,378 (GRCm39) |
splice site |
probably null |
|
R7763:Dnah5
|
UTSW |
15 |
28,314,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R7821:Dnah5
|
UTSW |
15 |
28,411,678 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7826:Dnah5
|
UTSW |
15 |
28,367,958 (GRCm39) |
missense |
probably damaging |
1.00 |
R7872:Dnah5
|
UTSW |
15 |
28,245,830 (GRCm39) |
missense |
probably damaging |
0.99 |
R7889:Dnah5
|
UTSW |
15 |
28,448,560 (GRCm39) |
nonsense |
probably null |
|
R7919:Dnah5
|
UTSW |
15 |
28,350,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R7920:Dnah5
|
UTSW |
15 |
28,453,368 (GRCm39) |
missense |
probably benign |
0.00 |
R7936:Dnah5
|
UTSW |
15 |
28,345,983 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7996:Dnah5
|
UTSW |
15 |
28,409,323 (GRCm39) |
missense |
probably damaging |
0.98 |
R8063:Dnah5
|
UTSW |
15 |
28,230,729 (GRCm39) |
missense |
probably benign |
|
R8084:Dnah5
|
UTSW |
15 |
28,388,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R8105:Dnah5
|
UTSW |
15 |
28,372,548 (GRCm39) |
missense |
probably benign |
|
R8114:Dnah5
|
UTSW |
15 |
28,240,122 (GRCm39) |
missense |
probably benign |
0.01 |
R8142:Dnah5
|
UTSW |
15 |
28,384,519 (GRCm39) |
missense |
probably benign |
0.36 |
R8153:Dnah5
|
UTSW |
15 |
28,384,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R8161:Dnah5
|
UTSW |
15 |
28,350,850 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8174:Dnah5
|
UTSW |
15 |
28,311,279 (GRCm39) |
splice site |
probably null |
|
R8187:Dnah5
|
UTSW |
15 |
28,384,355 (GRCm39) |
missense |
probably damaging |
1.00 |
R8194:Dnah5
|
UTSW |
15 |
28,453,414 (GRCm39) |
missense |
probably damaging |
0.99 |
R8280:Dnah5
|
UTSW |
15 |
28,408,538 (GRCm39) |
missense |
probably benign |
0.01 |
R8291:Dnah5
|
UTSW |
15 |
28,263,743 (GRCm39) |
missense |
probably benign |
0.03 |
R8324:Dnah5
|
UTSW |
15 |
28,347,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R8347:Dnah5
|
UTSW |
15 |
28,236,812 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8356:Dnah5
|
UTSW |
15 |
28,444,313 (GRCm39) |
missense |
probably benign |
0.03 |
R8356:Dnah5
|
UTSW |
15 |
28,444,469 (GRCm39) |
missense |
probably null |
0.02 |
R8361:Dnah5
|
UTSW |
15 |
28,331,956 (GRCm39) |
missense |
probably damaging |
0.98 |
R8375:Dnah5
|
UTSW |
15 |
28,327,489 (GRCm39) |
missense |
probably benign |
0.00 |
R8474:Dnah5
|
UTSW |
15 |
28,247,978 (GRCm39) |
missense |
probably benign |
0.00 |
R8481:Dnah5
|
UTSW |
15 |
28,419,941 (GRCm39) |
missense |
probably benign |
0.00 |
R8494:Dnah5
|
UTSW |
15 |
28,345,977 (GRCm39) |
missense |
probably benign |
0.32 |
R8495:Dnah5
|
UTSW |
15 |
28,409,414 (GRCm39) |
missense |
probably damaging |
0.97 |
R8519:Dnah5
|
UTSW |
15 |
28,299,245 (GRCm39) |
missense |
probably benign |
0.07 |
R8683:Dnah5
|
UTSW |
15 |
28,289,367 (GRCm39) |
missense |
probably benign |
0.00 |
R8739:Dnah5
|
UTSW |
15 |
28,346,006 (GRCm39) |
missense |
probably benign |
0.01 |
R8752:Dnah5
|
UTSW |
15 |
28,290,365 (GRCm39) |
missense |
probably benign |
0.00 |
R8784:Dnah5
|
UTSW |
15 |
28,388,097 (GRCm39) |
missense |
probably benign |
0.16 |
R8813:Dnah5
|
UTSW |
15 |
28,229,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R8862:Dnah5
|
UTSW |
15 |
28,459,502 (GRCm39) |
splice site |
probably benign |
|
R8873:Dnah5
|
UTSW |
15 |
28,219,334 (GRCm39) |
missense |
probably benign |
|
R8885:Dnah5
|
UTSW |
15 |
28,327,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R8901:Dnah5
|
UTSW |
15 |
28,365,715 (GRCm39) |
missense |
possibly damaging |
0.76 |
R9025:Dnah5
|
UTSW |
15 |
28,409,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R9037:Dnah5
|
UTSW |
15 |
28,248,104 (GRCm39) |
missense |
probably benign |
0.05 |
R9057:Dnah5
|
UTSW |
15 |
28,391,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R9059:Dnah5
|
UTSW |
15 |
28,245,812 (GRCm39) |
missense |
probably benign |
|
R9065:Dnah5
|
UTSW |
15 |
28,293,936 (GRCm39) |
missense |
probably benign |
0.09 |
R9098:Dnah5
|
UTSW |
15 |
28,420,107 (GRCm39) |
missense |
|
|
R9118:Dnah5
|
UTSW |
15 |
28,401,994 (GRCm39) |
frame shift |
probably null |
|
R9149:Dnah5
|
UTSW |
15 |
28,387,914 (GRCm39) |
missense |
probably benign |
0.00 |
R9184:Dnah5
|
UTSW |
15 |
28,340,552 (GRCm39) |
missense |
probably benign |
0.13 |
R9205:Dnah5
|
UTSW |
15 |
28,448,480 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9297:Dnah5
|
UTSW |
15 |
28,204,054 (GRCm39) |
start gained |
probably benign |
|
R9302:Dnah5
|
UTSW |
15 |
28,240,032 (GRCm39) |
missense |
probably benign |
0.03 |
R9310:Dnah5
|
UTSW |
15 |
28,448,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R9318:Dnah5
|
UTSW |
15 |
28,204,054 (GRCm39) |
start gained |
probably benign |
|
R9405:Dnah5
|
UTSW |
15 |
28,272,306 (GRCm39) |
missense |
probably benign |
|
R9424:Dnah5
|
UTSW |
15 |
28,272,286 (GRCm39) |
missense |
probably benign |
0.01 |
R9467:Dnah5
|
UTSW |
15 |
28,366,293 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9469:Dnah5
|
UTSW |
15 |
28,421,146 (GRCm39) |
missense |
probably benign |
0.06 |
R9548:Dnah5
|
UTSW |
15 |
28,328,025 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9564:Dnah5
|
UTSW |
15 |
28,290,422 (GRCm39) |
missense |
probably benign |
0.04 |
R9576:Dnah5
|
UTSW |
15 |
28,272,286 (GRCm39) |
missense |
probably benign |
0.01 |
R9593:Dnah5
|
UTSW |
15 |
28,236,774 (GRCm39) |
missense |
probably benign |
|
R9644:Dnah5
|
UTSW |
15 |
28,230,650 (GRCm39) |
missense |
probably damaging |
0.98 |
R9655:Dnah5
|
UTSW |
15 |
28,242,900 (GRCm39) |
missense |
probably benign |
|
R9657:Dnah5
|
UTSW |
15 |
28,410,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R9704:Dnah5
|
UTSW |
15 |
28,247,965 (GRCm39) |
missense |
probably benign |
0.00 |
R9797:Dnah5
|
UTSW |
15 |
28,233,316 (GRCm39) |
missense |
probably benign |
0.34 |
RF009:Dnah5
|
UTSW |
15 |
28,204,165 (GRCm39) |
missense |
probably benign |
0.00 |
X0011:Dnah5
|
UTSW |
15 |
28,408,527 (GRCm39) |
missense |
probably benign |
0.16 |
X0018:Dnah5
|
UTSW |
15 |
28,269,500 (GRCm39) |
missense |
probably benign |
0.00 |
X0022:Dnah5
|
UTSW |
15 |
28,270,557 (GRCm39) |
missense |
probably benign |
0.01 |
X0023:Dnah5
|
UTSW |
15 |
28,384,454 (GRCm39) |
missense |
probably damaging |
0.99 |
X0028:Dnah5
|
UTSW |
15 |
28,470,623 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Dnah5
|
UTSW |
15 |
28,366,503 (GRCm39) |
missense |
probably null |
0.10 |
Z1088:Dnah5
|
UTSW |
15 |
28,384,376 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Dnah5
|
UTSW |
15 |
28,295,457 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1177:Dnah5
|
UTSW |
15 |
28,270,549 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Dnah5
|
UTSW |
15 |
28,270,500 (GRCm39) |
missense |
probably benign |
0.32 |
Z1177:Dnah5
|
UTSW |
15 |
28,387,909 (GRCm39) |
missense |
possibly damaging |
0.72 |
|