Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alms1 |
A |
T |
6: 85,618,432 (GRCm39) |
D2826V |
probably damaging |
Het |
Alpl |
C |
T |
4: 137,469,945 (GRCm39) |
A460T |
probably damaging |
Het |
C2cd5 |
A |
G |
6: 142,976,963 (GRCm39) |
|
probably benign |
Het |
C4b |
C |
T |
17: 34,949,686 (GRCm39) |
R1468Q |
possibly damaging |
Het |
Calu |
A |
G |
6: 29,366,919 (GRCm39) |
T44A |
possibly damaging |
Het |
Cgn |
T |
C |
3: 94,685,326 (GRCm39) |
K399R |
probably benign |
Het |
Ciao3 |
A |
G |
17: 26,001,128 (GRCm39) |
H460R |
probably benign |
Het |
Cyp2t4 |
G |
A |
7: 26,857,228 (GRCm39) |
V356M |
probably damaging |
Het |
D430041D05Rik |
T |
C |
2: 104,044,604 (GRCm39) |
D683G |
probably damaging |
Het |
Dhcr24 |
T |
A |
4: 106,443,552 (GRCm39) |
I410N |
probably damaging |
Het |
Dmap1 |
T |
A |
4: 117,539,085 (GRCm39) |
E17V |
probably benign |
Het |
Dnaaf9 |
C |
T |
2: 130,554,286 (GRCm39) |
R921K |
probably benign |
Het |
Dnah7a |
A |
G |
1: 53,535,109 (GRCm39) |
I2717T |
possibly damaging |
Het |
Epb41l3 |
G |
T |
17: 69,554,741 (GRCm39) |
K280N |
probably damaging |
Het |
Espl1 |
T |
A |
15: 102,208,290 (GRCm39) |
M432K |
probably damaging |
Het |
Fgf5 |
C |
A |
5: 98,409,874 (GRCm39) |
A141E |
probably damaging |
Het |
Fto |
T |
A |
8: 92,211,795 (GRCm39) |
F373L |
probably damaging |
Het |
Gpatch1 |
T |
C |
7: 35,007,694 (GRCm39) |
D122G |
probably damaging |
Het |
Ints11 |
T |
C |
4: 155,972,568 (GRCm39) |
|
probably null |
Het |
Jarid2 |
A |
G |
13: 45,056,405 (GRCm39) |
Q398R |
probably benign |
Het |
Kcnh1 |
A |
G |
1: 191,959,208 (GRCm39) |
D254G |
probably damaging |
Het |
Lamc3 |
C |
T |
2: 31,825,738 (GRCm39) |
|
probably benign |
Het |
Lamc3 |
C |
T |
2: 31,825,737 (GRCm39) |
|
probably benign |
Het |
Ltbp4 |
T |
C |
7: 27,028,297 (GRCm39) |
|
probably null |
Het |
Mcm6 |
A |
G |
1: 128,267,119 (GRCm39) |
Y575H |
probably damaging |
Het |
Myh9 |
A |
C |
15: 77,671,826 (GRCm39) |
Y422D |
probably damaging |
Het |
Or4c35 |
T |
C |
2: 89,808,506 (GRCm39) |
L128P |
probably damaging |
Het |
Or5b105 |
A |
C |
19: 13,080,187 (GRCm39) |
N160K |
possibly damaging |
Het |
Or8b47 |
T |
C |
9: 38,435,021 (GRCm39) |
|
probably benign |
Het |
Plcb1 |
T |
C |
2: 135,206,682 (GRCm39) |
|
probably benign |
Het |
Pmfbp1 |
A |
G |
8: 110,246,881 (GRCm39) |
E251G |
probably damaging |
Het |
Psg27 |
A |
T |
7: 18,291,054 (GRCm39) |
V383E |
probably damaging |
Het |
Ptprn |
A |
T |
1: 75,224,517 (GRCm39) |
H946Q |
possibly damaging |
Het |
Rbl1 |
A |
G |
2: 157,009,333 (GRCm39) |
V734A |
probably benign |
Het |
Rspry1 |
T |
A |
8: 95,376,439 (GRCm39) |
N320K |
probably damaging |
Het |
Ryr1 |
A |
T |
7: 28,760,965 (GRCm39) |
V3219D |
probably damaging |
Het |
Ryr2 |
C |
A |
13: 11,774,721 (GRCm39) |
W1145L |
probably damaging |
Het |
Scel |
A |
T |
14: 103,813,683 (GRCm39) |
R319* |
probably null |
Het |
Stxbp2 |
C |
T |
8: 3,685,629 (GRCm39) |
T226I |
probably benign |
Het |
Tac1 |
A |
T |
6: 7,562,410 (GRCm39) |
N106I |
possibly damaging |
Het |
Trim13 |
G |
T |
14: 61,842,693 (GRCm39) |
|
probably null |
Het |
Tspan31 |
T |
G |
10: 126,904,778 (GRCm39) |
|
probably null |
Het |
Usp36 |
C |
T |
11: 118,155,609 (GRCm39) |
V723M |
probably benign |
Het |
Vcan |
G |
T |
13: 89,836,742 (GRCm39) |
T2934K |
probably damaging |
Het |
|
Other mutations in Utrn |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00333:Utrn
|
APN |
10 |
12,547,574 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00469:Utrn
|
APN |
10 |
12,282,273 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00518:Utrn
|
APN |
10 |
12,542,587 (GRCm39) |
splice site |
probably benign |
|
IGL00560:Utrn
|
APN |
10 |
12,331,211 (GRCm39) |
nonsense |
probably null |
|
IGL00589:Utrn
|
APN |
10 |
12,554,362 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL00662:Utrn
|
APN |
10 |
12,540,705 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00754:Utrn
|
APN |
10 |
12,539,236 (GRCm39) |
missense |
probably benign |
0.05 |
IGL00772:Utrn
|
APN |
10 |
12,524,929 (GRCm39) |
missense |
probably benign |
|
IGL00775:Utrn
|
APN |
10 |
12,620,974 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00782:Utrn
|
APN |
10 |
12,528,555 (GRCm39) |
missense |
probably benign |
0.13 |
IGL00962:Utrn
|
APN |
10 |
12,357,078 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL01584:Utrn
|
APN |
10 |
12,602,111 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01677:Utrn
|
APN |
10 |
12,619,901 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01695:Utrn
|
APN |
10 |
12,621,086 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01743:Utrn
|
APN |
10 |
12,587,301 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01815:Utrn
|
APN |
10 |
12,528,460 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01901:Utrn
|
APN |
10 |
12,516,672 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01982:Utrn
|
APN |
10 |
12,623,773 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01983:Utrn
|
APN |
10 |
12,545,525 (GRCm39) |
missense |
probably benign |
0.18 |
IGL02031:Utrn
|
APN |
10 |
12,610,948 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02106:Utrn
|
APN |
10 |
12,289,717 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02134:Utrn
|
APN |
10 |
12,519,163 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02209:Utrn
|
APN |
10 |
12,559,039 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02217:Utrn
|
APN |
10 |
12,627,303 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02250:Utrn
|
APN |
10 |
12,312,135 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02307:Utrn
|
APN |
10 |
12,625,809 (GRCm39) |
nonsense |
probably null |
|
IGL02386:Utrn
|
APN |
10 |
12,297,352 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02494:Utrn
|
APN |
10 |
12,585,798 (GRCm39) |
missense |
probably benign |
|
IGL02631:Utrn
|
APN |
10 |
12,585,807 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02729:Utrn
|
APN |
10 |
12,596,554 (GRCm39) |
unclassified |
probably benign |
|
IGL02736:Utrn
|
APN |
10 |
12,297,384 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02832:Utrn
|
APN |
10 |
12,613,937 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL03184:Utrn
|
APN |
10 |
12,585,910 (GRCm39) |
missense |
probably benign |
0.04 |
IGL03194:Utrn
|
APN |
10 |
12,282,173 (GRCm39) |
splice site |
probably benign |
|
IGL03346:Utrn
|
APN |
10 |
12,401,096 (GRCm39) |
missense |
probably benign |
0.22 |
retiring
|
UTSW |
10 |
12,516,764 (GRCm39) |
missense |
probably damaging |
1.00 |
shrinking_violet
|
UTSW |
10 |
12,587,329 (GRCm39) |
critical splice acceptor site |
probably null |
|
Wallflower
|
UTSW |
10 |
12,623,719 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4548:Utrn
|
UTSW |
10 |
12,509,685 (GRCm39) |
critical splice donor site |
probably benign |
|
I2288:Utrn
|
UTSW |
10 |
12,297,384 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4677001:Utrn
|
UTSW |
10 |
12,542,448 (GRCm39) |
missense |
probably benign |
0.06 |
R0022:Utrn
|
UTSW |
10 |
12,585,700 (GRCm39) |
splice site |
probably benign |
|
R0024:Utrn
|
UTSW |
10 |
12,281,755 (GRCm39) |
missense |
probably benign |
0.00 |
R0024:Utrn
|
UTSW |
10 |
12,281,755 (GRCm39) |
missense |
probably benign |
0.00 |
R0026:Utrn
|
UTSW |
10 |
12,601,940 (GRCm39) |
splice site |
probably benign |
|
R0026:Utrn
|
UTSW |
10 |
12,601,940 (GRCm39) |
splice site |
probably benign |
|
R0091:Utrn
|
UTSW |
10 |
12,610,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R0112:Utrn
|
UTSW |
10 |
12,562,209 (GRCm39) |
nonsense |
probably null |
|
R0126:Utrn
|
UTSW |
10 |
12,587,219 (GRCm39) |
missense |
probably benign |
0.02 |
R0184:Utrn
|
UTSW |
10 |
12,543,362 (GRCm39) |
missense |
probably benign |
|
R0219:Utrn
|
UTSW |
10 |
12,560,195 (GRCm39) |
missense |
probably damaging |
1.00 |
R0369:Utrn
|
UTSW |
10 |
12,509,766 (GRCm39) |
missense |
probably benign |
0.37 |
R0390:Utrn
|
UTSW |
10 |
12,585,804 (GRCm39) |
missense |
probably benign |
0.05 |
R0391:Utrn
|
UTSW |
10 |
12,401,077 (GRCm39) |
splice site |
probably benign |
|
R0408:Utrn
|
UTSW |
10 |
12,259,934 (GRCm39) |
makesense |
probably null |
|
R0409:Utrn
|
UTSW |
10 |
12,519,345 (GRCm39) |
missense |
probably benign |
0.01 |
R0441:Utrn
|
UTSW |
10 |
12,564,038 (GRCm39) |
missense |
probably null |
0.88 |
R0504:Utrn
|
UTSW |
10 |
12,278,639 (GRCm39) |
missense |
probably benign |
0.02 |
R0730:Utrn
|
UTSW |
10 |
12,573,902 (GRCm39) |
splice site |
probably benign |
|
R1078:Utrn
|
UTSW |
10 |
12,331,310 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1171:Utrn
|
UTSW |
10 |
12,357,052 (GRCm39) |
missense |
probably damaging |
0.99 |
R1191:Utrn
|
UTSW |
10 |
12,509,777 (GRCm39) |
missense |
probably benign |
0.02 |
R1203:Utrn
|
UTSW |
10 |
12,362,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R1401:Utrn
|
UTSW |
10 |
12,524,897 (GRCm39) |
missense |
probably benign |
|
R1418:Utrn
|
UTSW |
10 |
12,589,094 (GRCm39) |
missense |
probably benign |
|
R1439:Utrn
|
UTSW |
10 |
12,619,793 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1441:Utrn
|
UTSW |
10 |
12,559,039 (GRCm39) |
missense |
probably damaging |
0.97 |
R1445:Utrn
|
UTSW |
10 |
12,554,318 (GRCm39) |
splice site |
probably benign |
|
R1509:Utrn
|
UTSW |
10 |
12,331,185 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1546:Utrn
|
UTSW |
10 |
12,312,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R1585:Utrn
|
UTSW |
10 |
12,312,029 (GRCm39) |
missense |
possibly damaging |
0.62 |
R1621:Utrn
|
UTSW |
10 |
12,589,027 (GRCm39) |
missense |
probably benign |
0.24 |
R1637:Utrn
|
UTSW |
10 |
12,312,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R1703:Utrn
|
UTSW |
10 |
12,603,473 (GRCm39) |
splice site |
probably benign |
|
R1725:Utrn
|
UTSW |
10 |
12,539,263 (GRCm39) |
missense |
probably damaging |
0.99 |
R1735:Utrn
|
UTSW |
10 |
12,585,882 (GRCm39) |
missense |
probably benign |
|
R1770:Utrn
|
UTSW |
10 |
12,351,040 (GRCm39) |
missense |
probably damaging |
0.98 |
R1778:Utrn
|
UTSW |
10 |
12,312,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R1783:Utrn
|
UTSW |
10 |
12,339,083 (GRCm39) |
missense |
probably damaging |
1.00 |
R1818:Utrn
|
UTSW |
10 |
12,585,708 (GRCm39) |
critical splice donor site |
probably null |
|
R1829:Utrn
|
UTSW |
10 |
12,351,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R1919:Utrn
|
UTSW |
10 |
12,331,224 (GRCm39) |
missense |
probably benign |
0.15 |
R1964:Utrn
|
UTSW |
10 |
12,560,181 (GRCm39) |
missense |
probably damaging |
1.00 |
R2080:Utrn
|
UTSW |
10 |
12,612,826 (GRCm39) |
missense |
probably benign |
0.36 |
R2092:Utrn
|
UTSW |
10 |
12,554,442 (GRCm39) |
missense |
probably benign |
0.12 |
R2107:Utrn
|
UTSW |
10 |
12,312,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R2108:Utrn
|
UTSW |
10 |
12,312,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R2760:Utrn
|
UTSW |
10 |
12,566,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R2884:Utrn
|
UTSW |
10 |
12,615,105 (GRCm39) |
splice site |
probably null |
|
R2885:Utrn
|
UTSW |
10 |
12,615,105 (GRCm39) |
splice site |
probably null |
|
R2886:Utrn
|
UTSW |
10 |
12,615,105 (GRCm39) |
splice site |
probably null |
|
R2903:Utrn
|
UTSW |
10 |
12,519,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R2944:Utrn
|
UTSW |
10 |
12,519,163 (GRCm39) |
missense |
probably damaging |
1.00 |
R2945:Utrn
|
UTSW |
10 |
12,362,135 (GRCm39) |
missense |
possibly damaging |
0.50 |
R3438:Utrn
|
UTSW |
10 |
12,357,062 (GRCm39) |
missense |
probably damaging |
0.98 |
R3683:Utrn
|
UTSW |
10 |
12,542,579 (GRCm39) |
missense |
probably benign |
0.10 |
R3735:Utrn
|
UTSW |
10 |
12,354,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R3907:Utrn
|
UTSW |
10 |
12,585,926 (GRCm39) |
splice site |
probably benign |
|
R3923:Utrn
|
UTSW |
10 |
12,615,223 (GRCm39) |
missense |
probably benign |
0.23 |
R3925:Utrn
|
UTSW |
10 |
12,573,786 (GRCm39) |
missense |
probably benign |
|
R3926:Utrn
|
UTSW |
10 |
12,573,786 (GRCm39) |
missense |
probably benign |
|
R3938:Utrn
|
UTSW |
10 |
12,625,774 (GRCm39) |
critical splice donor site |
probably null |
|
R3941:Utrn
|
UTSW |
10 |
12,587,329 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3958:Utrn
|
UTSW |
10 |
12,625,852 (GRCm39) |
missense |
probably damaging |
1.00 |
R4091:Utrn
|
UTSW |
10 |
12,585,915 (GRCm39) |
missense |
probably benign |
0.10 |
R4454:Utrn
|
UTSW |
10 |
12,603,584 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4585:Utrn
|
UTSW |
10 |
12,564,050 (GRCm39) |
missense |
probably benign |
0.01 |
R4667:Utrn
|
UTSW |
10 |
12,573,797 (GRCm39) |
missense |
probably benign |
0.22 |
R4684:Utrn
|
UTSW |
10 |
12,620,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R4782:Utrn
|
UTSW |
10 |
12,625,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R4785:Utrn
|
UTSW |
10 |
12,530,489 (GRCm39) |
missense |
probably benign |
0.39 |
R4799:Utrn
|
UTSW |
10 |
12,625,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R4829:Utrn
|
UTSW |
10 |
12,539,205 (GRCm39) |
missense |
probably benign |
0.00 |
R4878:Utrn
|
UTSW |
10 |
12,603,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R4955:Utrn
|
UTSW |
10 |
12,737,311 (GRCm39) |
critical splice donor site |
probably null |
|
R4967:Utrn
|
UTSW |
10 |
12,331,164 (GRCm39) |
missense |
probably damaging |
0.99 |
R5071:Utrn
|
UTSW |
10 |
12,259,948 (GRCm39) |
splice site |
probably null |
|
R5072:Utrn
|
UTSW |
10 |
12,259,948 (GRCm39) |
splice site |
probably null |
|
R5186:Utrn
|
UTSW |
10 |
12,604,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R5213:Utrn
|
UTSW |
10 |
12,512,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R5296:Utrn
|
UTSW |
10 |
12,277,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R5309:Utrn
|
UTSW |
10 |
12,603,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R5312:Utrn
|
UTSW |
10 |
12,603,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R5399:Utrn
|
UTSW |
10 |
12,516,727 (GRCm39) |
missense |
probably damaging |
1.00 |
R5407:Utrn
|
UTSW |
10 |
12,556,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R5411:Utrn
|
UTSW |
10 |
12,524,929 (GRCm39) |
missense |
probably benign |
|
R5428:Utrn
|
UTSW |
10 |
12,569,175 (GRCm39) |
missense |
probably benign |
0.09 |
R5595:Utrn
|
UTSW |
10 |
12,558,062 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5602:Utrn
|
UTSW |
10 |
12,625,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R5608:Utrn
|
UTSW |
10 |
12,547,581 (GRCm39) |
missense |
probably benign |
0.00 |
R5678:Utrn
|
UTSW |
10 |
12,317,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R5726:Utrn
|
UTSW |
10 |
12,545,550 (GRCm39) |
missense |
probably benign |
|
R5804:Utrn
|
UTSW |
10 |
12,297,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R5916:Utrn
|
UTSW |
10 |
12,540,795 (GRCm39) |
missense |
probably damaging |
0.97 |
R5941:Utrn
|
UTSW |
10 |
12,362,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R6014:Utrn
|
UTSW |
10 |
12,566,620 (GRCm39) |
missense |
probably benign |
0.01 |
R6015:Utrn
|
UTSW |
10 |
12,354,168 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6028:Utrn
|
UTSW |
10 |
12,530,460 (GRCm39) |
missense |
probably benign |
0.00 |
R6158:Utrn
|
UTSW |
10 |
12,566,566 (GRCm39) |
missense |
probably benign |
0.04 |
R6181:Utrn
|
UTSW |
10 |
12,615,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R6300:Utrn
|
UTSW |
10 |
12,377,220 (GRCm39) |
missense |
probably benign |
0.35 |
R6367:Utrn
|
UTSW |
10 |
12,623,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R6377:Utrn
|
UTSW |
10 |
12,619,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R6434:Utrn
|
UTSW |
10 |
12,401,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R6498:Utrn
|
UTSW |
10 |
12,317,837 (GRCm39) |
missense |
probably benign |
|
R6579:Utrn
|
UTSW |
10 |
12,623,750 (GRCm39) |
missense |
probably benign |
0.05 |
R6704:Utrn
|
UTSW |
10 |
12,621,035 (GRCm39) |
missense |
probably damaging |
0.99 |
R6736:Utrn
|
UTSW |
10 |
12,497,047 (GRCm39) |
missense |
probably benign |
0.09 |
R6755:Utrn
|
UTSW |
10 |
12,574,831 (GRCm39) |
missense |
probably benign |
0.00 |
R6793:Utrn
|
UTSW |
10 |
12,574,844 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6793:Utrn
|
UTSW |
10 |
12,516,669 (GRCm39) |
critical splice donor site |
probably null |
|
R6835:Utrn
|
UTSW |
10 |
12,603,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R6919:Utrn
|
UTSW |
10 |
12,569,214 (GRCm39) |
nonsense |
probably null |
|
R6920:Utrn
|
UTSW |
10 |
12,626,214 (GRCm39) |
missense |
probably damaging |
0.98 |
R7037:Utrn
|
UTSW |
10 |
12,702,514 (GRCm39) |
splice site |
probably null |
|
R7038:Utrn
|
UTSW |
10 |
12,558,082 (GRCm39) |
missense |
probably damaging |
1.00 |
R7055:Utrn
|
UTSW |
10 |
12,623,665 (GRCm39) |
missense |
probably benign |
0.23 |
R7072:Utrn
|
UTSW |
10 |
12,340,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R7090:Utrn
|
UTSW |
10 |
12,560,260 (GRCm39) |
missense |
possibly damaging |
0.58 |
R7211:Utrn
|
UTSW |
10 |
12,277,079 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7248:Utrn
|
UTSW |
10 |
12,604,562 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7305:Utrn
|
UTSW |
10 |
12,261,280 (GRCm39) |
missense |
probably benign |
|
R7334:Utrn
|
UTSW |
10 |
12,603,753 (GRCm39) |
splice site |
probably null |
|
R7348:Utrn
|
UTSW |
10 |
12,623,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R7375:Utrn
|
UTSW |
10 |
12,516,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R7436:Utrn
|
UTSW |
10 |
12,315,535 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7476:Utrn
|
UTSW |
10 |
12,516,695 (GRCm39) |
missense |
probably benign |
|
R7514:Utrn
|
UTSW |
10 |
12,573,833 (GRCm39) |
missense |
probably benign |
0.00 |
R7527:Utrn
|
UTSW |
10 |
12,277,126 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7735:Utrn
|
UTSW |
10 |
12,619,787 (GRCm39) |
critical splice donor site |
probably null |
|
R7748:Utrn
|
UTSW |
10 |
12,490,252 (GRCm39) |
missense |
probably benign |
0.01 |
R7778:Utrn
|
UTSW |
10 |
12,362,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R7824:Utrn
|
UTSW |
10 |
12,362,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R7826:Utrn
|
UTSW |
10 |
12,277,050 (GRCm39) |
splice site |
probably null |
|
R7872:Utrn
|
UTSW |
10 |
12,573,873 (GRCm39) |
missense |
probably benign |
|
R7915:Utrn
|
UTSW |
10 |
12,340,956 (GRCm39) |
missense |
probably damaging |
1.00 |
R7922:Utrn
|
UTSW |
10 |
12,543,271 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8081:Utrn
|
UTSW |
10 |
12,423,803 (GRCm39) |
start gained |
probably benign |
|
R8132:Utrn
|
UTSW |
10 |
12,558,154 (GRCm39) |
missense |
probably damaging |
0.99 |
R8167:Utrn
|
UTSW |
10 |
12,547,558 (GRCm39) |
nonsense |
probably null |
|
R8186:Utrn
|
UTSW |
10 |
12,573,867 (GRCm39) |
missense |
probably benign |
|
R8331:Utrn
|
UTSW |
10 |
12,490,363 (GRCm39) |
missense |
probably benign |
0.00 |
R8352:Utrn
|
UTSW |
10 |
12,689,253 (GRCm39) |
missense |
probably benign |
0.34 |
R8408:Utrn
|
UTSW |
10 |
12,545,887 (GRCm39) |
missense |
possibly damaging |
0.69 |
R8452:Utrn
|
UTSW |
10 |
12,689,253 (GRCm39) |
missense |
probably benign |
0.34 |
R8478:Utrn
|
UTSW |
10 |
12,524,892 (GRCm39) |
missense |
probably benign |
|
R8489:Utrn
|
UTSW |
10 |
12,587,190 (GRCm39) |
missense |
probably benign |
0.05 |
R8516:Utrn
|
UTSW |
10 |
12,362,254 (GRCm39) |
missense |
probably damaging |
0.99 |
R8520:Utrn
|
UTSW |
10 |
12,545,930 (GRCm39) |
nonsense |
probably null |
|
R8550:Utrn
|
UTSW |
10 |
12,689,329 (GRCm39) |
intron |
probably benign |
|
R8856:Utrn
|
UTSW |
10 |
12,543,351 (GRCm39) |
missense |
probably benign |
|
R8881:Utrn
|
UTSW |
10 |
12,423,737 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9180:Utrn
|
UTSW |
10 |
12,545,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R9186:Utrn
|
UTSW |
10 |
12,490,318 (GRCm39) |
missense |
probably benign |
|
R9216:Utrn
|
UTSW |
10 |
12,689,229 (GRCm39) |
missense |
probably benign |
0.19 |
R9251:Utrn
|
UTSW |
10 |
12,512,531 (GRCm39) |
missense |
probably benign |
0.01 |
R9273:Utrn
|
UTSW |
10 |
12,509,707 (GRCm39) |
missense |
probably damaging |
0.97 |
R9307:Utrn
|
UTSW |
10 |
12,554,475 (GRCm39) |
missense |
probably benign |
0.02 |
R9344:Utrn
|
UTSW |
10 |
12,560,275 (GRCm39) |
missense |
probably benign |
0.17 |
R9419:Utrn
|
UTSW |
10 |
12,564,125 (GRCm39) |
missense |
probably damaging |
1.00 |
R9435:Utrn
|
UTSW |
10 |
12,519,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R9623:Utrn
|
UTSW |
10 |
12,282,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R9650:Utrn
|
UTSW |
10 |
12,613,929 (GRCm39) |
missense |
probably benign |
0.00 |
R9653:Utrn
|
UTSW |
10 |
12,539,189 (GRCm39) |
missense |
probably benign |
0.41 |
R9653:Utrn
|
UTSW |
10 |
12,497,123 (GRCm39) |
missense |
probably benign |
0.17 |
R9672:Utrn
|
UTSW |
10 |
12,603,613 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9678:Utrn
|
UTSW |
10 |
12,615,159 (GRCm39) |
missense |
probably benign |
0.00 |
R9741:Utrn
|
UTSW |
10 |
12,702,564 (GRCm39) |
missense |
probably benign |
|
R9765:Utrn
|
UTSW |
10 |
12,610,921 (GRCm39) |
missense |
probably damaging |
0.99 |
R9799:Utrn
|
UTSW |
10 |
12,585,736 (GRCm39) |
missense |
probably benign |
0.01 |
RF009:Utrn
|
UTSW |
10 |
12,509,689 (GRCm39) |
nonsense |
probably null |
|
V1662:Utrn
|
UTSW |
10 |
12,297,384 (GRCm39) |
missense |
probably damaging |
1.00 |
X0018:Utrn
|
UTSW |
10 |
12,610,942 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Utrn
|
UTSW |
10 |
12,564,173 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1176:Utrn
|
UTSW |
10 |
12,558,104 (GRCm39) |
nonsense |
probably null |
|
Z1177:Utrn
|
UTSW |
10 |
12,497,123 (GRCm39) |
missense |
probably benign |
0.17 |
Z1177:Utrn
|
UTSW |
10 |
12,401,150 (GRCm39) |
nonsense |
probably null |
|
Z1186:Utrn
|
UTSW |
10 |
12,545,491 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1189:Utrn
|
UTSW |
10 |
12,545,491 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1191:Utrn
|
UTSW |
10 |
12,545,491 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1192:Utrn
|
UTSW |
10 |
12,545,491 (GRCm39) |
missense |
probably damaging |
1.00 |
|