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 |
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 Ubr4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00087:Ubr4
|
APN |
4 |
139,192,633 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL00336:Ubr4
|
APN |
4 |
139,155,877 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00586:Ubr4
|
APN |
4 |
139,182,495 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL00659:Ubr4
|
APN |
4 |
139,148,556 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00766:Ubr4
|
APN |
4 |
139,168,077 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00819:Ubr4
|
APN |
4 |
139,203,593 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL00833:Ubr4
|
APN |
4 |
139,120,470 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01126:Ubr4
|
APN |
4 |
139,129,866 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01311:Ubr4
|
APN |
4 |
139,206,356 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL01349:Ubr4
|
APN |
4 |
139,208,039 (GRCm39) |
missense |
unknown |
|
IGL01388:Ubr4
|
APN |
4 |
139,187,554 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL01417:Ubr4
|
APN |
4 |
139,138,111 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01446:Ubr4
|
APN |
4 |
139,165,351 (GRCm39) |
splice site |
probably benign |
|
IGL01449:Ubr4
|
APN |
4 |
139,140,047 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01545:Ubr4
|
APN |
4 |
139,170,140 (GRCm39) |
splice site |
probably benign |
|
IGL01568:Ubr4
|
APN |
4 |
139,148,684 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01596:Ubr4
|
APN |
4 |
139,189,845 (GRCm39) |
splice site |
probably benign |
|
IGL01621:Ubr4
|
APN |
4 |
139,168,094 (GRCm39) |
nonsense |
probably null |
|
IGL01639:Ubr4
|
APN |
4 |
139,144,655 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01655:Ubr4
|
APN |
4 |
139,135,107 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01710:Ubr4
|
APN |
4 |
139,145,772 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL01830:Ubr4
|
APN |
4 |
139,199,811 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01862:Ubr4
|
APN |
4 |
139,204,469 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL01868:Ubr4
|
APN |
4 |
139,139,989 (GRCm39) |
nonsense |
probably null |
|
IGL01874:Ubr4
|
APN |
4 |
139,120,600 (GRCm39) |
splice site |
probably benign |
|
IGL01889:Ubr4
|
APN |
4 |
139,189,783 (GRCm39) |
nonsense |
probably null |
|
IGL01891:Ubr4
|
APN |
4 |
139,163,571 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01980:Ubr4
|
APN |
4 |
139,156,913 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02126:Ubr4
|
APN |
4 |
139,180,052 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02153:Ubr4
|
APN |
4 |
139,187,471 (GRCm39) |
nonsense |
probably null |
|
IGL02173:Ubr4
|
APN |
4 |
139,164,381 (GRCm39) |
splice site |
probably null |
|
IGL02214:Ubr4
|
APN |
4 |
139,155,894 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02214:Ubr4
|
APN |
4 |
139,189,138 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02220:Ubr4
|
APN |
4 |
139,115,746 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02246:Ubr4
|
APN |
4 |
139,186,414 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02264:Ubr4
|
APN |
4 |
139,182,939 (GRCm39) |
nonsense |
probably null |
|
IGL02273:Ubr4
|
APN |
4 |
139,199,889 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02316:Ubr4
|
APN |
4 |
139,200,489 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL02328:Ubr4
|
APN |
4 |
139,206,233 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02476:Ubr4
|
APN |
4 |
139,148,560 (GRCm39) |
nonsense |
probably null |
|
IGL02477:Ubr4
|
APN |
4 |
139,163,516 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02544:Ubr4
|
APN |
4 |
139,142,429 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02622:Ubr4
|
APN |
4 |
139,194,561 (GRCm39) |
nonsense |
probably null |
|
IGL02679:Ubr4
|
APN |
4 |
139,186,445 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02728:Ubr4
|
APN |
4 |
139,196,122 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02754:Ubr4
|
APN |
4 |
139,138,095 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02754:Ubr4
|
APN |
4 |
139,120,470 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02892:Ubr4
|
APN |
4 |
139,144,642 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02897:Ubr4
|
APN |
4 |
139,199,819 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02946:Ubr4
|
APN |
4 |
139,152,606 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02964:Ubr4
|
APN |
4 |
139,135,131 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL03059:Ubr4
|
APN |
4 |
139,207,987 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03068:Ubr4
|
APN |
4 |
139,137,041 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03087:Ubr4
|
APN |
4 |
139,177,668 (GRCm39) |
nonsense |
probably null |
|
IGL03116:Ubr4
|
APN |
4 |
139,206,892 (GRCm39) |
splice site |
probably benign |
|
IGL03212:Ubr4
|
APN |
4 |
139,137,074 (GRCm39) |
missense |
probably benign |
0.13 |
IGL03228:Ubr4
|
APN |
4 |
139,156,909 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03292:Ubr4
|
APN |
4 |
139,167,746 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03388:Ubr4
|
APN |
4 |
139,142,343 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03393:Ubr4
|
APN |
4 |
139,179,989 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03409:Ubr4
|
APN |
4 |
139,127,240 (GRCm39) |
nonsense |
probably null |
|
Aqua_regia
|
UTSW |
4 |
139,180,030 (GRCm39) |
nonsense |
probably null |
|
Eats
|
UTSW |
4 |
139,190,886 (GRCm39) |
missense |
probably damaging |
0.97 |
Hardened
|
UTSW |
4 |
139,196,158 (GRCm39) |
missense |
probably damaging |
1.00 |
Stoney
|
UTSW |
4 |
139,171,998 (GRCm39) |
missense |
probably damaging |
1.00 |
Uber
|
UTSW |
4 |
139,206,373 (GRCm39) |
critical splice donor site |
probably null |
|
BB001:Ubr4
|
UTSW |
4 |
139,194,587 (GRCm39) |
missense |
unknown |
|
BB011:Ubr4
|
UTSW |
4 |
139,194,587 (GRCm39) |
missense |
unknown |
|
P0019:Ubr4
|
UTSW |
4 |
139,179,092 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4544001:Ubr4
|
UTSW |
4 |
139,129,871 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0001:Ubr4
|
UTSW |
4 |
139,179,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R0002:Ubr4
|
UTSW |
4 |
139,118,211 (GRCm39) |
missense |
probably damaging |
1.00 |
R0006:Ubr4
|
UTSW |
4 |
139,158,960 (GRCm39) |
missense |
probably benign |
0.03 |
R0006:Ubr4
|
UTSW |
4 |
139,158,960 (GRCm39) |
missense |
probably benign |
0.03 |
R0008:Ubr4
|
UTSW |
4 |
139,157,487 (GRCm39) |
missense |
probably damaging |
1.00 |
R0027:Ubr4
|
UTSW |
4 |
139,127,704 (GRCm39) |
missense |
probably damaging |
0.99 |
R0027:Ubr4
|
UTSW |
4 |
139,127,704 (GRCm39) |
missense |
probably damaging |
0.99 |
R0030:Ubr4
|
UTSW |
4 |
139,154,104 (GRCm39) |
missense |
probably damaging |
1.00 |
R0044:Ubr4
|
UTSW |
4 |
139,164,369 (GRCm39) |
splice site |
probably benign |
|
R0044:Ubr4
|
UTSW |
4 |
139,164,369 (GRCm39) |
splice site |
probably benign |
|
R0088:Ubr4
|
UTSW |
4 |
139,168,125 (GRCm39) |
missense |
probably damaging |
1.00 |
R0131:Ubr4
|
UTSW |
4 |
139,191,362 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0184:Ubr4
|
UTSW |
4 |
139,172,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R0219:Ubr4
|
UTSW |
4 |
139,157,568 (GRCm39) |
missense |
possibly damaging |
0.64 |
R0227:Ubr4
|
UTSW |
4 |
139,158,960 (GRCm39) |
missense |
probably benign |
0.03 |
R0270:Ubr4
|
UTSW |
4 |
139,206,746 (GRCm39) |
splice site |
probably benign |
|
R0285:Ubr4
|
UTSW |
4 |
139,168,112 (GRCm39) |
missense |
probably damaging |
1.00 |
R0322:Ubr4
|
UTSW |
4 |
139,149,729 (GRCm39) |
missense |
probably damaging |
1.00 |
R0363:Ubr4
|
UTSW |
4 |
139,119,171 (GRCm39) |
missense |
probably damaging |
0.98 |
R0393:Ubr4
|
UTSW |
4 |
139,138,171 (GRCm39) |
splice site |
probably benign |
|
R0450:Ubr4
|
UTSW |
4 |
139,157,534 (GRCm39) |
missense |
probably benign |
0.14 |
R0504:Ubr4
|
UTSW |
4 |
139,133,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R0504:Ubr4
|
UTSW |
4 |
139,208,149 (GRCm39) |
critical splice donor site |
probably null |
|
R0510:Ubr4
|
UTSW |
4 |
139,157,534 (GRCm39) |
missense |
probably benign |
0.14 |
R0513:Ubr4
|
UTSW |
4 |
139,144,186 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0517:Ubr4
|
UTSW |
4 |
139,119,435 (GRCm39) |
missense |
probably benign |
0.00 |
R0558:Ubr4
|
UTSW |
4 |
139,154,213 (GRCm39) |
missense |
probably benign |
0.09 |
R0617:Ubr4
|
UTSW |
4 |
139,206,373 (GRCm39) |
critical splice donor site |
probably null |
|
R0636:Ubr4
|
UTSW |
4 |
139,163,613 (GRCm39) |
splice site |
probably null |
|
R0637:Ubr4
|
UTSW |
4 |
139,126,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R0652:Ubr4
|
UTSW |
4 |
139,128,637 (GRCm39) |
missense |
probably damaging |
0.99 |
R0691:Ubr4
|
UTSW |
4 |
139,151,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R0729:Ubr4
|
UTSW |
4 |
139,212,631 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0735:Ubr4
|
UTSW |
4 |
139,155,339 (GRCm39) |
splice site |
probably null |
|
R0751:Ubr4
|
UTSW |
4 |
139,164,509 (GRCm39) |
splice site |
probably benign |
|
R0789:Ubr4
|
UTSW |
4 |
139,137,582 (GRCm39) |
critical splice donor site |
probably null |
|
R0825:Ubr4
|
UTSW |
4 |
139,206,887 (GRCm39) |
critical splice donor site |
probably null |
|
R0828:Ubr4
|
UTSW |
4 |
139,177,864 (GRCm39) |
splice site |
probably benign |
|
R1052:Ubr4
|
UTSW |
4 |
139,182,771 (GRCm39) |
missense |
possibly damaging |
0.83 |
R1184:Ubr4
|
UTSW |
4 |
139,164,509 (GRCm39) |
splice site |
probably benign |
|
R1222:Ubr4
|
UTSW |
4 |
139,115,782 (GRCm39) |
splice site |
probably null |
|
R1258:Ubr4
|
UTSW |
4 |
139,154,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R1321:Ubr4
|
UTSW |
4 |
139,187,434 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1385:Ubr4
|
UTSW |
4 |
139,129,923 (GRCm39) |
missense |
probably benign |
0.00 |
R1450:Ubr4
|
UTSW |
4 |
139,195,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R1470:Ubr4
|
UTSW |
4 |
139,148,537 (GRCm39) |
splice site |
probably null |
|
R1470:Ubr4
|
UTSW |
4 |
139,148,537 (GRCm39) |
splice site |
probably null |
|
R1474:Ubr4
|
UTSW |
4 |
139,156,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R1479:Ubr4
|
UTSW |
4 |
139,153,151 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1534:Ubr4
|
UTSW |
4 |
139,155,462 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1546:Ubr4
|
UTSW |
4 |
139,144,238 (GRCm39) |
nonsense |
probably null |
|
R1786:Ubr4
|
UTSW |
4 |
139,151,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R1789:Ubr4
|
UTSW |
4 |
139,120,364 (GRCm39) |
missense |
probably damaging |
1.00 |
R1796:Ubr4
|
UTSW |
4 |
139,155,907 (GRCm39) |
missense |
probably benign |
0.25 |
R1800:Ubr4
|
UTSW |
4 |
139,135,274 (GRCm39) |
missense |
probably damaging |
0.99 |
R1801:Ubr4
|
UTSW |
4 |
139,179,874 (GRCm39) |
splice site |
probably null |
|
R1827:Ubr4
|
UTSW |
4 |
139,153,008 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1887:Ubr4
|
UTSW |
4 |
139,182,871 (GRCm39) |
missense |
probably damaging |
1.00 |
R1966:Ubr4
|
UTSW |
4 |
139,178,555 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2010:Ubr4
|
UTSW |
4 |
139,207,963 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2049:Ubr4
|
UTSW |
4 |
139,204,518 (GRCm39) |
missense |
probably damaging |
0.97 |
R2069:Ubr4
|
UTSW |
4 |
139,206,851 (GRCm39) |
missense |
possibly damaging |
0.66 |
R2114:Ubr4
|
UTSW |
4 |
139,156,922 (GRCm39) |
nonsense |
probably null |
|
R2140:Ubr4
|
UTSW |
4 |
139,204,518 (GRCm39) |
missense |
probably damaging |
0.97 |
R2141:Ubr4
|
UTSW |
4 |
139,204,518 (GRCm39) |
missense |
probably damaging |
0.97 |
R2142:Ubr4
|
UTSW |
4 |
139,204,518 (GRCm39) |
missense |
probably damaging |
0.97 |
R2168:Ubr4
|
UTSW |
4 |
139,137,960 (GRCm39) |
missense |
probably benign |
0.25 |
R2237:Ubr4
|
UTSW |
4 |
139,170,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R2249:Ubr4
|
UTSW |
4 |
139,176,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R2261:Ubr4
|
UTSW |
4 |
139,140,773 (GRCm39) |
missense |
probably damaging |
0.99 |
R2264:Ubr4
|
UTSW |
4 |
139,147,684 (GRCm39) |
splice site |
probably benign |
|
R2353:Ubr4
|
UTSW |
4 |
139,160,984 (GRCm39) |
missense |
possibly damaging |
0.48 |
R2437:Ubr4
|
UTSW |
4 |
139,200,853 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2496:Ubr4
|
UTSW |
4 |
139,200,516 (GRCm39) |
unclassified |
probably benign |
|
R2896:Ubr4
|
UTSW |
4 |
139,182,955 (GRCm39) |
splice site |
probably null |
|
R2922:Ubr4
|
UTSW |
4 |
139,206,811 (GRCm39) |
missense |
possibly damaging |
0.66 |
R2972:Ubr4
|
UTSW |
4 |
139,133,847 (GRCm39) |
missense |
probably benign |
0.22 |
R2973:Ubr4
|
UTSW |
4 |
139,133,847 (GRCm39) |
missense |
probably benign |
0.22 |
R2989:Ubr4
|
UTSW |
4 |
139,190,869 (GRCm39) |
missense |
possibly damaging |
0.89 |
R3176:Ubr4
|
UTSW |
4 |
139,149,166 (GRCm39) |
missense |
probably benign |
0.03 |
R3276:Ubr4
|
UTSW |
4 |
139,149,166 (GRCm39) |
missense |
probably benign |
0.03 |
R3772:Ubr4
|
UTSW |
4 |
139,180,011 (GRCm39) |
missense |
possibly damaging |
0.89 |
R3844:Ubr4
|
UTSW |
4 |
139,186,437 (GRCm39) |
missense |
probably damaging |
0.99 |
R3873:Ubr4
|
UTSW |
4 |
139,151,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R3900:Ubr4
|
UTSW |
4 |
139,206,373 (GRCm39) |
critical splice donor site |
probably null |
|
R3951:Ubr4
|
UTSW |
4 |
139,120,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R4020:Ubr4
|
UTSW |
4 |
139,179,116 (GRCm39) |
missense |
probably damaging |
0.98 |
R4178:Ubr4
|
UTSW |
4 |
139,120,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R4308:Ubr4
|
UTSW |
4 |
139,199,820 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4378:Ubr4
|
UTSW |
4 |
139,137,751 (GRCm39) |
missense |
possibly damaging |
0.76 |
R4400:Ubr4
|
UTSW |
4 |
139,189,167 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4421:Ubr4
|
UTSW |
4 |
139,189,167 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4462:Ubr4
|
UTSW |
4 |
139,145,813 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4583:Ubr4
|
UTSW |
4 |
139,108,164 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4611:Ubr4
|
UTSW |
4 |
139,126,890 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4664:Ubr4
|
UTSW |
4 |
139,133,829 (GRCm39) |
missense |
possibly damaging |
0.56 |
R4671:Ubr4
|
UTSW |
4 |
139,163,502 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4672:Ubr4
|
UTSW |
4 |
139,138,027 (GRCm39) |
missense |
probably damaging |
0.99 |
R4673:Ubr4
|
UTSW |
4 |
139,138,027 (GRCm39) |
missense |
probably damaging |
0.99 |
R4696:Ubr4
|
UTSW |
4 |
139,135,983 (GRCm39) |
missense |
probably benign |
0.09 |
R4701:Ubr4
|
UTSW |
4 |
139,198,647 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4705:Ubr4
|
UTSW |
4 |
139,177,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R4726:Ubr4
|
UTSW |
4 |
139,209,890 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4728:Ubr4
|
UTSW |
4 |
139,151,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R4783:Ubr4
|
UTSW |
4 |
139,149,044 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4833:Ubr4
|
UTSW |
4 |
139,129,857 (GRCm39) |
missense |
probably damaging |
0.98 |
R4892:Ubr4
|
UTSW |
4 |
139,155,828 (GRCm39) |
missense |
probably benign |
0.14 |
R4936:Ubr4
|
UTSW |
4 |
139,123,877 (GRCm39) |
missense |
probably damaging |
0.98 |
R5000:Ubr4
|
UTSW |
4 |
139,163,480 (GRCm39) |
missense |
probably damaging |
0.98 |
R5114:Ubr4
|
UTSW |
4 |
139,137,934 (GRCm39) |
missense |
probably damaging |
0.99 |
R5189:Ubr4
|
UTSW |
4 |
139,137,960 (GRCm39) |
missense |
probably benign |
0.25 |
R5197:Ubr4
|
UTSW |
4 |
139,195,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R5213:Ubr4
|
UTSW |
4 |
139,129,877 (GRCm39) |
nonsense |
probably null |
|
R5219:Ubr4
|
UTSW |
4 |
139,204,543 (GRCm39) |
nonsense |
probably null |
|
R5346:Ubr4
|
UTSW |
4 |
139,155,802 (GRCm39) |
missense |
probably damaging |
0.97 |
R5368:Ubr4
|
UTSW |
4 |
139,124,839 (GRCm39) |
intron |
probably benign |
|
R5442:Ubr4
|
UTSW |
4 |
139,135,083 (GRCm39) |
missense |
probably damaging |
1.00 |
R5527:Ubr4
|
UTSW |
4 |
139,208,099 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5548:Ubr4
|
UTSW |
4 |
139,187,401 (GRCm39) |
missense |
probably damaging |
0.97 |
R5568:Ubr4
|
UTSW |
4 |
139,119,349 (GRCm39) |
missense |
probably damaging |
0.99 |
R5639:Ubr4
|
UTSW |
4 |
139,179,959 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5643:Ubr4
|
UTSW |
4 |
139,171,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R5663:Ubr4
|
UTSW |
4 |
139,155,894 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5755:Ubr4
|
UTSW |
4 |
139,187,406 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5781:Ubr4
|
UTSW |
4 |
139,195,407 (GRCm39) |
missense |
probably damaging |
1.00 |
R5784:Ubr4
|
UTSW |
4 |
139,152,529 (GRCm39) |
missense |
probably damaging |
1.00 |
R5817:Ubr4
|
UTSW |
4 |
139,196,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R5872:Ubr4
|
UTSW |
4 |
139,152,641 (GRCm39) |
missense |
probably damaging |
0.98 |
R5891:Ubr4
|
UTSW |
4 |
139,135,937 (GRCm39) |
nonsense |
probably null |
|
R5901:Ubr4
|
UTSW |
4 |
139,178,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R5958:Ubr4
|
UTSW |
4 |
139,182,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R5974:Ubr4
|
UTSW |
4 |
139,148,389 (GRCm39) |
splice site |
probably null |
|
R6065:Ubr4
|
UTSW |
4 |
139,148,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R6109:Ubr4
|
UTSW |
4 |
139,144,675 (GRCm39) |
missense |
probably damaging |
0.99 |
R6207:Ubr4
|
UTSW |
4 |
139,148,559 (GRCm39) |
missense |
probably damaging |
1.00 |
R6265:Ubr4
|
UTSW |
4 |
139,179,951 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6319:Ubr4
|
UTSW |
4 |
139,136,200 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6342:Ubr4
|
UTSW |
4 |
139,156,850 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6434:Ubr4
|
UTSW |
4 |
139,156,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R6437:Ubr4
|
UTSW |
4 |
139,124,525 (GRCm39) |
critical splice donor site |
probably null |
|
R6481:Ubr4
|
UTSW |
4 |
139,159,062 (GRCm39) |
missense |
probably damaging |
0.97 |
R6502:Ubr4
|
UTSW |
4 |
139,171,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R6546:Ubr4
|
UTSW |
4 |
139,141,705 (GRCm39) |
missense |
probably damaging |
0.99 |
R6603:Ubr4
|
UTSW |
4 |
139,182,897 (GRCm39) |
missense |
probably benign |
0.17 |
R6648:Ubr4
|
UTSW |
4 |
139,180,030 (GRCm39) |
nonsense |
probably null |
|
R6649:Ubr4
|
UTSW |
4 |
139,200,935 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6653:Ubr4
|
UTSW |
4 |
139,200,935 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6668:Ubr4
|
UTSW |
4 |
139,192,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R6770:Ubr4
|
UTSW |
4 |
139,216,493 (GRCm39) |
missense |
unknown |
|
R6772:Ubr4
|
UTSW |
4 |
139,194,541 (GRCm39) |
nonsense |
probably null |
|
R6857:Ubr4
|
UTSW |
4 |
139,213,362 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6869:Ubr4
|
UTSW |
4 |
139,194,538 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6912:Ubr4
|
UTSW |
4 |
139,185,545 (GRCm39) |
critical splice donor site |
probably null |
|
R6943:Ubr4
|
UTSW |
4 |
139,164,442 (GRCm39) |
nonsense |
probably null |
|
R6970:Ubr4
|
UTSW |
4 |
139,133,839 (GRCm39) |
nonsense |
probably null |
|
R6976:Ubr4
|
UTSW |
4 |
139,120,388 (GRCm39) |
missense |
probably damaging |
0.98 |
R7000:Ubr4
|
UTSW |
4 |
139,141,715 (GRCm39) |
missense |
probably damaging |
1.00 |
R7017:Ubr4
|
UTSW |
4 |
139,120,401 (GRCm39) |
missense |
probably damaging |
0.99 |
R7165:Ubr4
|
UTSW |
4 |
139,177,824 (GRCm39) |
missense |
|
|
R7222:Ubr4
|
UTSW |
4 |
139,190,684 (GRCm39) |
missense |
unknown |
|
R7241:Ubr4
|
UTSW |
4 |
139,170,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R7343:Ubr4
|
UTSW |
4 |
139,140,749 (GRCm39) |
missense |
probably benign |
0.09 |
R7367:Ubr4
|
UTSW |
4 |
139,180,002 (GRCm39) |
missense |
unknown |
|
R7393:Ubr4
|
UTSW |
4 |
139,154,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R7432:Ubr4
|
UTSW |
4 |
139,115,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R7448:Ubr4
|
UTSW |
4 |
139,189,778 (GRCm39) |
missense |
unknown |
|
R7502:Ubr4
|
UTSW |
4 |
139,139,983 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7514:Ubr4
|
UTSW |
4 |
139,179,966 (GRCm39) |
missense |
unknown |
|
R7526:Ubr4
|
UTSW |
4 |
139,149,728 (GRCm39) |
missense |
probably benign |
0.00 |
R7529:Ubr4
|
UTSW |
4 |
139,149,728 (GRCm39) |
missense |
probably benign |
0.00 |
R7666:Ubr4
|
UTSW |
4 |
139,140,791 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7699:Ubr4
|
UTSW |
4 |
139,136,178 (GRCm39) |
nonsense |
probably null |
|
R7700:Ubr4
|
UTSW |
4 |
139,136,178 (GRCm39) |
nonsense |
probably null |
|
R7726:Ubr4
|
UTSW |
4 |
139,186,231 (GRCm39) |
missense |
unknown |
|
R7753:Ubr4
|
UTSW |
4 |
139,197,603 (GRCm39) |
missense |
unknown |
|
R7810:Ubr4
|
UTSW |
4 |
139,142,394 (GRCm39) |
missense |
|
|
R7837:Ubr4
|
UTSW |
4 |
139,120,462 (GRCm39) |
nonsense |
probably null |
|
R7868:Ubr4
|
UTSW |
4 |
139,187,344 (GRCm39) |
missense |
unknown |
|
R7872:Ubr4
|
UTSW |
4 |
139,120,373 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7887:Ubr4
|
UTSW |
4 |
139,135,121 (GRCm39) |
missense |
probably damaging |
0.99 |
R7924:Ubr4
|
UTSW |
4 |
139,194,587 (GRCm39) |
missense |
unknown |
|
R7980:Ubr4
|
UTSW |
4 |
139,145,717 (GRCm39) |
missense |
|
|
R7982:Ubr4
|
UTSW |
4 |
139,155,519 (GRCm39) |
critical splice donor site |
probably null |
|
R8005:Ubr4
|
UTSW |
4 |
139,139,941 (GRCm39) |
missense |
probably damaging |
0.98 |
R8054:Ubr4
|
UTSW |
4 |
139,195,413 (GRCm39) |
missense |
unknown |
|
R8094:Ubr4
|
UTSW |
4 |
139,168,007 (GRCm39) |
missense |
probably damaging |
0.97 |
R8151:Ubr4
|
UTSW |
4 |
139,130,112 (GRCm39) |
missense |
probably damaging |
0.97 |
R8183:Ubr4
|
UTSW |
4 |
139,209,782 (GRCm39) |
missense |
unknown |
|
R8252:Ubr4
|
UTSW |
4 |
139,200,528 (GRCm39) |
missense |
unknown |
|
R8505:Ubr4
|
UTSW |
4 |
139,156,880 (GRCm39) |
missense |
|
|
R8519:Ubr4
|
UTSW |
4 |
139,143,958 (GRCm39) |
missense |
probably damaging |
0.97 |
R8716:Ubr4
|
UTSW |
4 |
139,196,164 (GRCm39) |
missense |
unknown |
|
R8720:Ubr4
|
UTSW |
4 |
139,208,149 (GRCm39) |
critical splice donor site |
probably null |
|
R8749:Ubr4
|
UTSW |
4 |
139,129,935 (GRCm39) |
missense |
probably damaging |
0.98 |
R8768:Ubr4
|
UTSW |
4 |
139,149,076 (GRCm39) |
missense |
|
|
R8789:Ubr4
|
UTSW |
4 |
139,137,494 (GRCm39) |
missense |
possibly damaging |
0.76 |
R8879:Ubr4
|
UTSW |
4 |
139,137,829 (GRCm39) |
missense |
probably benign |
0.06 |
R8937:Ubr4
|
UTSW |
4 |
139,190,886 (GRCm39) |
missense |
probably damaging |
0.97 |
R9006:Ubr4
|
UTSW |
4 |
139,172,003 (GRCm39) |
critical splice donor site |
probably null |
|
R9116:Ubr4
|
UTSW |
4 |
139,145,785 (GRCm39) |
missense |
|
|
R9134:Ubr4
|
UTSW |
4 |
139,127,755 (GRCm39) |
critical splice donor site |
probably null |
|
R9251:Ubr4
|
UTSW |
4 |
139,177,636 (GRCm39) |
missense |
|
|
R9340:Ubr4
|
UTSW |
4 |
139,182,763 (GRCm39) |
missense |
unknown |
|
R9384:Ubr4
|
UTSW |
4 |
139,194,631 (GRCm39) |
missense |
unknown |
|
R9389:Ubr4
|
UTSW |
4 |
139,153,235 (GRCm39) |
missense |
|
|
R9393:Ubr4
|
UTSW |
4 |
139,212,613 (GRCm39) |
missense |
unknown |
|
R9531:Ubr4
|
UTSW |
4 |
139,135,217 (GRCm39) |
missense |
probably benign |
0.00 |
R9573:Ubr4
|
UTSW |
4 |
139,148,450 (GRCm39) |
missense |
|
|
R9604:Ubr4
|
UTSW |
4 |
139,159,827 (GRCm39) |
critical splice donor site |
probably null |
|
R9613:Ubr4
|
UTSW |
4 |
139,149,073 (GRCm39) |
missense |
|
|
R9623:Ubr4
|
UTSW |
4 |
139,159,024 (GRCm39) |
missense |
probably benign |
0.00 |
R9651:Ubr4
|
UTSW |
4 |
139,206,859 (GRCm39) |
missense |
unknown |
|
R9685:Ubr4
|
UTSW |
4 |
139,191,341 (GRCm39) |
missense |
unknown |
|
R9698:Ubr4
|
UTSW |
4 |
139,167,975 (GRCm39) |
missense |
|
|
R9700:Ubr4
|
UTSW |
4 |
139,119,388 (GRCm39) |
missense |
probably damaging |
0.97 |
R9727:Ubr4
|
UTSW |
4 |
139,140,735 (GRCm39) |
missense |
probably damaging |
0.98 |
R9766:Ubr4
|
UTSW |
4 |
139,194,595 (GRCm39) |
missense |
unknown |
|
T0975:Ubr4
|
UTSW |
4 |
139,179,092 (GRCm39) |
missense |
probably damaging |
1.00 |
X0028:Ubr4
|
UTSW |
4 |
139,137,582 (GRCm39) |
critical splice donor site |
probably null |
|
Z1176:Ubr4
|
UTSW |
4 |
139,137,456 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Ubr4
|
UTSW |
4 |
139,129,971 (GRCm39) |
missense |
probably benign |
0.04 |
Z1176:Ubr4
|
UTSW |
4 |
139,127,696 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Ubr4
|
UTSW |
4 |
139,177,792 (GRCm39) |
missense |
|
|
Z1186:Ubr4
|
UTSW |
4 |
139,137,964 (GRCm39) |
missense |
probably benign |
0.02 |
|