Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actl11 |
A |
T |
9: 107,805,844 (GRCm39) |
I56F |
possibly damaging |
Het |
Adgrl3 |
G |
T |
5: 81,942,348 (GRCm39) |
R1357L |
possibly damaging |
Het |
Alpk1 |
T |
A |
3: 127,522,961 (GRCm39) |
D27V |
probably damaging |
Het |
Als2 |
T |
C |
1: 59,225,175 (GRCm39) |
E986G |
probably damaging |
Het |
Ankle2 |
T |
A |
5: 110,400,818 (GRCm39) |
L717Q |
possibly damaging |
Het |
Arl8b |
A |
G |
6: 108,760,285 (GRCm39) |
T24A |
possibly damaging |
Het |
Atp2a1 |
A |
G |
7: 126,047,502 (GRCm39) |
I718T |
probably damaging |
Het |
Atp6v0e2 |
T |
A |
6: 48,517,031 (GRCm39) |
N70K |
probably benign |
Het |
Bcl11a |
A |
G |
11: 24,115,086 (GRCm39) |
S810G |
probably damaging |
Het |
Bcl2a1d |
T |
G |
9: 88,605,488 (GRCm39) |
*173S |
probably null |
Het |
Bltp1 |
A |
T |
3: 37,087,426 (GRCm39) |
D511V |
possibly damaging |
Het |
Cacna1g |
A |
G |
11: 94,317,278 (GRCm39) |
Y1494H |
probably damaging |
Het |
Ccdc7a |
T |
C |
8: 129,487,850 (GRCm39) |
K186E |
possibly damaging |
Het |
Cfap43 |
T |
C |
19: 47,764,515 (GRCm39) |
I817V |
probably benign |
Het |
Chd5 |
C |
T |
4: 152,441,147 (GRCm39) |
R196* |
probably null |
Het |
Chsy1 |
C |
T |
7: 65,820,748 (GRCm39) |
H328Y |
probably benign |
Het |
Clcn3 |
A |
T |
8: 61,372,522 (GRCm39) |
S713T |
probably benign |
Het |
Csrnp3 |
A |
T |
2: 65,708,400 (GRCm39) |
|
probably null |
Het |
Dnhd1 |
A |
G |
7: 105,332,001 (GRCm39) |
N86S |
probably benign |
Het |
Epha3 |
T |
C |
16: 63,593,444 (GRCm39) |
T215A |
probably damaging |
Het |
Fgf1 |
T |
C |
18: 38,987,944 (GRCm39) |
|
probably null |
Het |
Fosl1 |
T |
C |
19: 5,504,947 (GRCm39) |
S145P |
probably damaging |
Het |
Frem3 |
T |
A |
8: 81,338,187 (GRCm39) |
V160E |
probably damaging |
Het |
Galk2 |
A |
T |
2: 125,771,505 (GRCm39) |
K177* |
probably null |
Het |
Gria1 |
T |
C |
11: 57,200,668 (GRCm39) |
Y782H |
probably damaging |
Het |
Gria4 |
C |
T |
9: 4,793,882 (GRCm39) |
E59K |
probably damaging |
Het |
Ighv1-11 |
A |
G |
12: 114,575,919 (GRCm39) |
Y99H |
possibly damaging |
Het |
Insm2 |
A |
T |
12: 55,647,330 (GRCm39) |
Y358F |
probably damaging |
Het |
Marveld3 |
C |
T |
8: 110,688,600 (GRCm39) |
G47D |
probably damaging |
Het |
Mthfd1l |
A |
G |
10: 4,098,064 (GRCm39) |
D967G |
probably damaging |
Het |
Nav2 |
G |
T |
7: 49,111,733 (GRCm39) |
M746I |
probably damaging |
Het |
Niban1 |
C |
A |
1: 151,512,263 (GRCm39) |
T55K |
possibly damaging |
Het |
Nmnat1 |
A |
G |
4: 149,557,841 (GRCm39) |
I67T |
possibly damaging |
Het |
Nub1 |
G |
T |
5: 24,906,422 (GRCm39) |
R316L |
probably benign |
Het |
Nxn |
A |
G |
11: 76,164,869 (GRCm39) |
V214A |
probably damaging |
Het |
Or52n5 |
C |
A |
7: 104,588,477 (GRCm39) |
S248Y |
probably benign |
Het |
Pelp1 |
A |
T |
11: 70,285,146 (GRCm39) |
D907E |
unknown |
Het |
Pik3c2a |
A |
T |
7: 116,017,584 (GRCm39) |
S58T |
probably damaging |
Het |
Pik3ca |
A |
G |
3: 32,505,997 (GRCm39) |
N703S |
probably benign |
Het |
Polr3c |
G |
A |
3: 96,624,066 (GRCm39) |
|
probably benign |
Het |
Pon1 |
C |
T |
6: 5,185,318 (GRCm39) |
G61R |
probably damaging |
Het |
Pou2f1 |
A |
T |
1: 165,759,287 (GRCm39) |
M1K |
probably null |
Het |
Prkdc |
T |
A |
16: 15,466,788 (GRCm39) |
C90S |
probably benign |
Het |
Prokr1 |
A |
G |
6: 87,558,330 (GRCm39) |
Y352H |
probably benign |
Het |
Rhod |
C |
T |
19: 4,476,719 (GRCm39) |
R134H |
probably damaging |
Het |
Rufy3 |
C |
T |
5: 88,762,895 (GRCm39) |
R110W |
probably damaging |
Het |
Sema4c |
A |
T |
1: 36,590,871 (GRCm39) |
M460K |
probably benign |
Het |
Slc46a3 |
T |
C |
5: 147,815,963 (GRCm39) |
S455G |
probably benign |
Het |
Smyd1 |
A |
T |
6: 71,193,811 (GRCm39) |
H371Q |
probably damaging |
Het |
Steap1 |
A |
G |
5: 5,786,432 (GRCm39) |
M335T |
probably benign |
Het |
Suox |
A |
G |
10: 128,506,921 (GRCm39) |
V369A |
probably damaging |
Het |
Thbs2 |
T |
C |
17: 14,900,666 (GRCm39) |
I514V |
probably benign |
Het |
Tie1 |
A |
T |
4: 118,341,979 (GRCm39) |
|
probably null |
Het |
Tmem131l |
T |
C |
3: 83,805,769 (GRCm39) |
E1558G |
probably damaging |
Het |
Tpcn1 |
G |
T |
5: 120,698,386 (GRCm39) |
H45Q |
probably benign |
Het |
Ush1c |
A |
G |
7: 45,870,857 (GRCm39) |
S327P |
probably damaging |
Het |
Ush2a |
G |
A |
1: 188,175,429 (GRCm39) |
V1176M |
possibly damaging |
Het |
Vmn1r50 |
G |
T |
6: 90,085,071 (GRCm39) |
C272F |
probably benign |
Het |
Vmn2r10 |
A |
T |
5: 109,143,636 (GRCm39) |
N771K |
probably damaging |
Het |
Vmn2r2 |
A |
T |
3: 64,024,257 (GRCm39) |
F691I |
possibly damaging |
Het |
Vmn2r53 |
T |
C |
7: 12,340,281 (GRCm39) |
Q64R |
probably benign |
Het |
Vmn2r95 |
G |
T |
17: 18,672,544 (GRCm39) |
L760F |
probably damaging |
Het |
Wdr97 |
T |
C |
15: 76,247,629 (GRCm39) |
|
probably null |
Het |
Xdh |
C |
A |
17: 74,213,053 (GRCm39) |
E863D |
probably benign |
Het |
Ykt6 |
A |
G |
11: 5,912,407 (GRCm39) |
Y120C |
possibly damaging |
Het |
Zranb2 |
A |
G |
3: 157,251,745 (GRCm39) |
*321W |
probably null |
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 |
IGL02926:Utrn
|
APN |
10 |
12,566,504 (GRCm39) |
missense |
probably damaging |
0.96 |
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 |
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 |
|