Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921509C19Rik |
A |
G |
2: 151,314,728 (GRCm39) |
F317L |
possibly damaging |
Het |
Abcc4 |
A |
G |
14: 118,905,811 (GRCm39) |
I85T |
probably benign |
Het |
Acoxl |
G |
T |
2: 127,917,810 (GRCm39) |
C498F |
probably damaging |
Het |
Akap13 |
C |
T |
7: 75,399,178 (GRCm39) |
T2752I |
probably damaging |
Het |
Anks6 |
C |
T |
4: 47,030,795 (GRCm39) |
G601S |
probably damaging |
Het |
Ap2a2 |
T |
G |
7: 141,210,061 (GRCm39) |
F836C |
probably damaging |
Het |
Atp2c1 |
A |
G |
9: 105,320,149 (GRCm39) |
V404A |
probably benign |
Het |
Atp7b |
G |
T |
8: 22,510,901 (GRCm39) |
A415E |
probably damaging |
Het |
Babam2 |
A |
T |
5: 31,942,927 (GRCm39) |
I71L |
possibly damaging |
Het |
Bean1 |
A |
G |
8: 104,943,606 (GRCm39) |
T54A |
probably damaging |
Het |
Cacna1b |
T |
A |
2: 24,508,330 (GRCm39) |
I1816F |
probably damaging |
Het |
Cacna1b |
C |
T |
2: 24,547,378 (GRCm39) |
G1202D |
probably damaging |
Het |
Casp8ap2 |
A |
G |
4: 32,640,554 (GRCm39) |
E536G |
probably damaging |
Het |
Cfap57 |
A |
G |
4: 118,470,262 (GRCm39) |
V206A |
probably benign |
Het |
Clca3a2 |
A |
T |
3: 144,783,640 (GRCm39) |
D658E |
probably damaging |
Het |
Cwc22 |
A |
T |
2: 77,726,653 (GRCm39) |
S809T |
probably benign |
Het |
Cyp2c54 |
C |
T |
19: 40,060,585 (GRCm39) |
R132Q |
possibly damaging |
Het |
Ddx20 |
A |
T |
3: 105,587,921 (GRCm39) |
D386E |
possibly damaging |
Het |
Ddx50 |
T |
C |
10: 62,478,632 (GRCm39) |
T185A |
probably damaging |
Het |
Decr1 |
G |
A |
4: 15,930,976 (GRCm39) |
R119* |
probably null |
Het |
Dennd4a |
T |
C |
9: 64,813,285 (GRCm39) |
S1415P |
probably benign |
Het |
Dnah12 |
A |
T |
14: 26,437,855 (GRCm39) |
I495L |
probably benign |
Het |
Dnah2 |
G |
A |
11: 69,346,799 (GRCm39) |
Q2596* |
probably null |
Het |
Dnajb13 |
A |
G |
7: 100,156,707 (GRCm39) |
L123S |
probably benign |
Het |
Drgx |
G |
T |
14: 32,369,101 (GRCm39) |
|
probably benign |
Het |
Elavl3 |
G |
A |
9: 21,948,107 (GRCm39) |
P19L |
probably benign |
Het |
Fer1l6 |
T |
C |
15: 58,443,250 (GRCm39) |
S518P |
probably benign |
Het |
Fgd3 |
T |
C |
13: 49,420,105 (GRCm39) |
S591G |
probably benign |
Het |
Galnt18 |
C |
A |
7: 111,071,271 (GRCm39) |
R566L |
probably benign |
Het |
Galnt6 |
A |
T |
15: 100,594,455 (GRCm39) |
Y525* |
probably null |
Het |
Gm10036 |
A |
T |
18: 15,966,359 (GRCm39) |
Y170F |
probably benign |
Het |
Hacd2 |
A |
G |
16: 34,842,921 (GRCm39) |
D24G |
unknown |
Het |
Idh3a |
T |
C |
9: 54,503,325 (GRCm39) |
M128T |
possibly damaging |
Het |
Ido1 |
C |
T |
8: 25,074,565 (GRCm39) |
M359I |
probably benign |
Het |
Ikbkb |
T |
C |
8: 23,171,693 (GRCm39) |
T185A |
probably damaging |
Het |
Insl6 |
C |
T |
19: 29,299,019 (GRCm39) |
G131D |
probably damaging |
Het |
Irgm1 |
A |
C |
11: 48,757,159 (GRCm39) |
S217R |
possibly damaging |
Het |
Itga11 |
T |
A |
9: 62,668,850 (GRCm39) |
Y702* |
probably null |
Het |
Itgb4 |
C |
T |
11: 115,874,983 (GRCm39) |
R447W |
probably benign |
Het |
Kansl2 |
T |
C |
15: 98,429,724 (GRCm39) |
M103V |
probably benign |
Het |
Kcnq2 |
T |
C |
2: 180,753,836 (GRCm39) |
N258S |
possibly damaging |
Het |
Kdm5d |
A |
T |
Y: 940,624 (GRCm39) |
D1045V |
probably damaging |
Het |
Lats2 |
A |
G |
14: 57,937,049 (GRCm39) |
L480P |
probably damaging |
Het |
Lin28b |
T |
A |
10: 45,296,736 (GRCm39) |
K87N |
possibly damaging |
Het |
Lpgat1 |
T |
A |
1: 191,451,682 (GRCm39) |
W103R |
probably damaging |
Het |
Lpl |
G |
T |
8: 69,347,345 (GRCm39) |
G166C |
probably damaging |
Het |
Ly75 |
A |
T |
2: 60,182,469 (GRCm39) |
Y569N |
probably damaging |
Het |
Mcm8 |
A |
T |
2: 132,680,689 (GRCm39) |
E564D |
probably damaging |
Het |
Me2 |
G |
T |
18: 73,918,847 (GRCm39) |
N411K |
probably damaging |
Het |
Mn1 |
A |
G |
5: 111,602,652 (GRCm39) |
T1297A |
possibly damaging |
Het |
Mphosph8 |
T |
A |
14: 56,916,046 (GRCm39) |
F447L |
probably benign |
Het |
Nacad |
T |
A |
11: 6,549,169 (GRCm39) |
D1294V |
probably damaging |
Het |
Neu3 |
A |
T |
7: 99,472,615 (GRCm39) |
F41I |
probably damaging |
Het |
Nlrp6 |
G |
T |
7: 140,503,497 (GRCm39) |
L534F |
probably damaging |
Het |
Nrap |
A |
G |
19: 56,366,575 (GRCm39) |
M338T |
probably damaging |
Het |
Nuak1 |
T |
C |
10: 84,210,979 (GRCm39) |
K370E |
probably damaging |
Het |
Or10ab4 |
T |
A |
7: 107,654,647 (GRCm39) |
C153S |
probably benign |
Het |
Or4d10 |
T |
A |
19: 12,051,639 (GRCm39) |
D119V |
probably damaging |
Het |
Or5w8 |
A |
G |
2: 87,687,632 (GRCm39) |
T38A |
probably benign |
Het |
Or6c212 |
C |
T |
10: 129,558,592 (GRCm39) |
V274M |
probably damaging |
Het |
P3h3 |
T |
C |
6: 124,818,736 (GRCm39) |
S701G |
probably benign |
Het |
Pdss2 |
T |
C |
10: 43,174,908 (GRCm39) |
M138T |
possibly damaging |
Het |
Piezo1 |
C |
T |
8: 123,213,220 (GRCm39) |
E1848K |
probably benign |
Het |
Prmt3 |
T |
G |
7: 49,476,557 (GRCm39) |
S389A |
probably benign |
Het |
Ptgis |
A |
G |
2: 167,067,194 (GRCm39) |
|
probably null |
Het |
Ptpn20 |
T |
C |
14: 33,336,416 (GRCm39) |
V85A |
probably benign |
Het |
Rabepk |
A |
T |
2: 34,670,669 (GRCm39) |
Y264N |
probably damaging |
Het |
Ralgapa2 |
A |
T |
2: 146,276,754 (GRCm39) |
C495* |
probably null |
Het |
Satb2 |
A |
G |
1: 56,930,327 (GRCm39) |
I232T |
probably benign |
Het |
Selenbp2 |
A |
T |
3: 94,610,856 (GRCm39) |
L307F |
probably damaging |
Het |
Sgpl1 |
T |
G |
10: 60,949,863 (GRCm39) |
Y112S |
probably damaging |
Het |
Slitrk5 |
T |
C |
14: 111,918,679 (GRCm39) |
S768P |
probably benign |
Het |
Smc3 |
T |
A |
19: 53,619,948 (GRCm39) |
Y615N |
probably damaging |
Het |
Spag17 |
A |
G |
3: 99,934,939 (GRCm39) |
N715S |
probably benign |
Het |
Spats2 |
A |
G |
15: 99,110,157 (GRCm39) |
E518G |
probably benign |
Het |
Spats2l |
A |
G |
1: 57,924,983 (GRCm39) |
H127R |
possibly damaging |
Het |
Tenm3 |
T |
A |
8: 48,731,996 (GRCm39) |
K1287* |
probably null |
Het |
Thoc1 |
T |
A |
18: 9,962,387 (GRCm39) |
S91T |
probably benign |
Het |
Thoc6 |
C |
T |
17: 23,888,911 (GRCm39) |
G166S |
probably damaging |
Het |
Tmem107 |
C |
A |
11: 68,962,087 (GRCm39) |
T42N |
possibly damaging |
Het |
Tmprss11c |
A |
G |
5: 86,385,569 (GRCm39) |
I288T |
probably damaging |
Het |
Tnrc18 |
A |
G |
5: 142,725,248 (GRCm39) |
F1827S |
unknown |
Het |
Trmt112 |
C |
A |
19: 6,887,566 (GRCm39) |
T5N |
probably damaging |
Het |
Trp53bp1 |
A |
T |
2: 121,101,027 (GRCm39) |
M57K |
probably benign |
Het |
Ttbk2 |
C |
A |
2: 120,575,631 (GRCm39) |
Q1115H |
probably damaging |
Het |
Ttn |
C |
A |
2: 76,559,989 (GRCm39) |
E27725* |
probably null |
Het |
Ttn |
A |
G |
2: 76,774,453 (GRCm39) |
M2151T |
probably damaging |
Het |
Usp9y |
A |
T |
Y: 1,384,336 (GRCm39) |
D727E |
probably damaging |
Het |
Vps13c |
A |
G |
9: 67,781,173 (GRCm39) |
T221A |
probably damaging |
Het |
Zbtb20 |
A |
G |
16: 43,439,055 (GRCm39) |
D725G |
probably damaging |
Het |
Zfp341 |
A |
T |
2: 154,468,734 (GRCm39) |
I126F |
possibly damaging |
Het |
Zfyve16 |
C |
T |
13: 92,650,402 (GRCm39) |
A861T |
probably damaging |
Het |
|
Other mutations in Prune2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00234:Prune2
|
APN |
19 |
17,145,708 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00848:Prune2
|
APN |
19 |
17,096,482 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00862:Prune2
|
APN |
19 |
17,096,713 (GRCm39) |
missense |
probably benign |
0.41 |
IGL00915:Prune2
|
APN |
19 |
16,993,617 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01084:Prune2
|
APN |
19 |
17,095,573 (GRCm39) |
missense |
probably benign |
0.19 |
IGL01109:Prune2
|
APN |
19 |
17,101,243 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01372:Prune2
|
APN |
19 |
17,102,433 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01650:Prune2
|
APN |
19 |
17,145,656 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01752:Prune2
|
APN |
19 |
17,101,267 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL01812:Prune2
|
APN |
19 |
16,981,141 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL01902:Prune2
|
APN |
19 |
17,096,002 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02195:Prune2
|
APN |
19 |
17,096,921 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02502:Prune2
|
APN |
19 |
17,101,245 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02569:Prune2
|
APN |
19 |
17,156,223 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02693:Prune2
|
APN |
19 |
17,101,855 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02737:Prune2
|
APN |
19 |
17,170,775 (GRCm39) |
nonsense |
probably null |
|
IGL02794:Prune2
|
APN |
19 |
17,096,725 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02985:Prune2
|
APN |
19 |
16,993,723 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03349:Prune2
|
APN |
19 |
17,100,710 (GRCm39) |
missense |
probably damaging |
1.00 |
3-1:Prune2
|
UTSW |
19 |
17,102,646 (GRCm39) |
missense |
probably benign |
0.00 |
R0060:Prune2
|
UTSW |
19 |
16,981,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R0098:Prune2
|
UTSW |
19 |
17,101,267 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0098:Prune2
|
UTSW |
19 |
17,101,267 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0165:Prune2
|
UTSW |
19 |
17,099,974 (GRCm39) |
missense |
probably benign |
0.00 |
R0277:Prune2
|
UTSW |
19 |
17,098,753 (GRCm39) |
missense |
probably damaging |
0.99 |
R0321:Prune2
|
UTSW |
19 |
17,099,818 (GRCm39) |
missense |
probably benign |
0.39 |
R0321:Prune2
|
UTSW |
19 |
17,098,291 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0374:Prune2
|
UTSW |
19 |
17,098,274 (GRCm39) |
missense |
probably benign |
0.00 |
R0380:Prune2
|
UTSW |
19 |
17,101,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R0396:Prune2
|
UTSW |
19 |
17,100,444 (GRCm39) |
missense |
probably benign |
0.35 |
R0408:Prune2
|
UTSW |
19 |
17,099,674 (GRCm39) |
missense |
probably benign |
0.00 |
R0421:Prune2
|
UTSW |
19 |
17,100,675 (GRCm39) |
missense |
probably benign |
0.02 |
R0480:Prune2
|
UTSW |
19 |
16,984,156 (GRCm39) |
splice site |
probably benign |
|
R0531:Prune2
|
UTSW |
19 |
16,984,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R0546:Prune2
|
UTSW |
19 |
16,998,030 (GRCm39) |
splice site |
probably benign |
|
R0554:Prune2
|
UTSW |
19 |
17,102,582 (GRCm39) |
nonsense |
probably null |
|
R0659:Prune2
|
UTSW |
19 |
17,100,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R0699:Prune2
|
UTSW |
19 |
17,101,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R0781:Prune2
|
UTSW |
19 |
17,102,586 (GRCm39) |
missense |
probably benign |
|
R1110:Prune2
|
UTSW |
19 |
17,102,586 (GRCm39) |
missense |
probably benign |
|
R1178:Prune2
|
UTSW |
19 |
17,100,469 (GRCm39) |
missense |
probably benign |
0.22 |
R1181:Prune2
|
UTSW |
19 |
17,100,469 (GRCm39) |
missense |
probably benign |
0.22 |
R1337:Prune2
|
UTSW |
19 |
17,096,971 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1356:Prune2
|
UTSW |
19 |
17,189,681 (GRCm39) |
missense |
probably benign |
0.40 |
R1385:Prune2
|
UTSW |
19 |
17,102,312 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1659:Prune2
|
UTSW |
19 |
17,098,015 (GRCm39) |
missense |
possibly damaging |
0.59 |
R1738:Prune2
|
UTSW |
19 |
17,102,374 (GRCm39) |
missense |
probably benign |
0.01 |
R1756:Prune2
|
UTSW |
19 |
17,101,068 (GRCm39) |
missense |
probably benign |
0.01 |
R1765:Prune2
|
UTSW |
19 |
17,102,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R1782:Prune2
|
UTSW |
19 |
17,099,537 (GRCm39) |
missense |
probably benign |
0.00 |
R1817:Prune2
|
UTSW |
19 |
17,099,445 (GRCm39) |
missense |
probably benign |
0.00 |
R1838:Prune2
|
UTSW |
19 |
17,177,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R1851:Prune2
|
UTSW |
19 |
17,176,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R1852:Prune2
|
UTSW |
19 |
17,176,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R1866:Prune2
|
UTSW |
19 |
17,100,856 (GRCm39) |
missense |
probably damaging |
1.00 |
R1911:Prune2
|
UTSW |
19 |
17,091,038 (GRCm39) |
missense |
probably benign |
0.02 |
R1983:Prune2
|
UTSW |
19 |
16,998,006 (GRCm39) |
missense |
probably damaging |
0.97 |
R2014:Prune2
|
UTSW |
19 |
17,097,887 (GRCm39) |
missense |
probably damaging |
1.00 |
R2066:Prune2
|
UTSW |
19 |
17,098,042 (GRCm39) |
missense |
possibly damaging |
0.57 |
R2088:Prune2
|
UTSW |
19 |
17,097,109 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2111:Prune2
|
UTSW |
19 |
17,185,602 (GRCm39) |
missense |
probably damaging |
1.00 |
R2128:Prune2
|
UTSW |
19 |
17,099,786 (GRCm39) |
missense |
probably benign |
0.00 |
R2165:Prune2
|
UTSW |
19 |
17,097,546 (GRCm39) |
missense |
probably benign |
0.19 |
R2241:Prune2
|
UTSW |
19 |
17,100,456 (GRCm39) |
missense |
probably damaging |
0.96 |
R2278:Prune2
|
UTSW |
19 |
17,095,919 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2504:Prune2
|
UTSW |
19 |
16,977,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R2508:Prune2
|
UTSW |
19 |
17,099,986 (GRCm39) |
missense |
probably benign |
0.43 |
R3055:Prune2
|
UTSW |
19 |
17,102,407 (GRCm39) |
missense |
probably damaging |
0.98 |
R3086:Prune2
|
UTSW |
19 |
17,098,777 (GRCm39) |
missense |
possibly damaging |
0.75 |
R3104:Prune2
|
UTSW |
19 |
17,096,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R3105:Prune2
|
UTSW |
19 |
17,096,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R3547:Prune2
|
UTSW |
19 |
17,101,712 (GRCm39) |
missense |
probably damaging |
0.96 |
R3702:Prune2
|
UTSW |
19 |
17,156,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R3753:Prune2
|
UTSW |
19 |
17,102,818 (GRCm39) |
missense |
probably benign |
0.38 |
R3933:Prune2
|
UTSW |
19 |
17,101,318 (GRCm39) |
missense |
probably damaging |
1.00 |
R3935:Prune2
|
UTSW |
19 |
17,177,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R4022:Prune2
|
UTSW |
19 |
16,977,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R4042:Prune2
|
UTSW |
19 |
16,981,190 (GRCm39) |
critical splice donor site |
probably null |
|
R4164:Prune2
|
UTSW |
19 |
16,981,098 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4453:Prune2
|
UTSW |
19 |
17,099,274 (GRCm39) |
missense |
probably benign |
0.00 |
R4642:Prune2
|
UTSW |
19 |
16,998,019 (GRCm39) |
critical splice donor site |
probably null |
|
R4661:Prune2
|
UTSW |
19 |
16,977,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R4666:Prune2
|
UTSW |
19 |
17,097,552 (GRCm39) |
nonsense |
probably null |
|
R4823:Prune2
|
UTSW |
19 |
17,097,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R4897:Prune2
|
UTSW |
19 |
17,099,219 (GRCm39) |
missense |
probably benign |
0.03 |
R4922:Prune2
|
UTSW |
19 |
17,100,116 (GRCm39) |
missense |
probably benign |
0.00 |
R5026:Prune2
|
UTSW |
19 |
17,176,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R5042:Prune2
|
UTSW |
19 |
17,097,161 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5124:Prune2
|
UTSW |
19 |
17,177,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R5133:Prune2
|
UTSW |
19 |
16,980,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R5184:Prune2
|
UTSW |
19 |
17,193,721 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5234:Prune2
|
UTSW |
19 |
17,096,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R5339:Prune2
|
UTSW |
19 |
17,098,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R5363:Prune2
|
UTSW |
19 |
17,095,630 (GRCm39) |
missense |
probably damaging |
1.00 |
R5382:Prune2
|
UTSW |
19 |
16,981,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R5436:Prune2
|
UTSW |
19 |
16,998,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R5480:Prune2
|
UTSW |
19 |
17,098,311 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5635:Prune2
|
UTSW |
19 |
17,095,573 (GRCm39) |
missense |
probably benign |
0.19 |
R5678:Prune2
|
UTSW |
19 |
17,096,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R5814:Prune2
|
UTSW |
19 |
16,993,725 (GRCm39) |
splice site |
probably null |
|
R5894:Prune2
|
UTSW |
19 |
17,098,755 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6011:Prune2
|
UTSW |
19 |
17,096,080 (GRCm39) |
missense |
probably benign |
0.35 |
R6207:Prune2
|
UTSW |
19 |
17,095,480 (GRCm39) |
missense |
probably damaging |
1.00 |
R6218:Prune2
|
UTSW |
19 |
17,098,926 (GRCm39) |
missense |
probably benign |
0.00 |
R6573:Prune2
|
UTSW |
19 |
17,098,522 (GRCm39) |
missense |
possibly damaging |
0.61 |
R6573:Prune2
|
UTSW |
19 |
17,098,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R6734:Prune2
|
UTSW |
19 |
16,981,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R6805:Prune2
|
UTSW |
19 |
17,097,954 (GRCm39) |
missense |
probably benign |
|
R6837:Prune2
|
UTSW |
19 |
17,156,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R6850:Prune2
|
UTSW |
19 |
17,099,552 (GRCm39) |
missense |
probably benign |
0.00 |
R6858:Prune2
|
UTSW |
19 |
17,095,470 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6874:Prune2
|
UTSW |
19 |
17,100,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R6954:Prune2
|
UTSW |
19 |
16,977,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R7098:Prune2
|
UTSW |
19 |
17,097,966 (GRCm39) |
missense |
probably benign |
0.39 |
R7102:Prune2
|
UTSW |
19 |
17,098,577 (GRCm39) |
missense |
probably benign |
0.24 |
R7246:Prune2
|
UTSW |
19 |
17,098,732 (GRCm39) |
missense |
probably damaging |
0.99 |
R7284:Prune2
|
UTSW |
19 |
17,097,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R7295:Prune2
|
UTSW |
19 |
17,097,261 (GRCm39) |
missense |
probably benign |
0.01 |
R7371:Prune2
|
UTSW |
19 |
17,096,734 (GRCm39) |
missense |
probably benign |
0.02 |
R7651:Prune2
|
UTSW |
19 |
17,097,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R7830:Prune2
|
UTSW |
19 |
17,100,038 (GRCm39) |
missense |
probably benign |
0.21 |
R7872:Prune2
|
UTSW |
19 |
17,096,798 (GRCm39) |
missense |
probably benign |
0.05 |
R7881:Prune2
|
UTSW |
19 |
17,100,393 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7966:Prune2
|
UTSW |
19 |
17,156,223 (GRCm39) |
missense |
probably damaging |
0.99 |
R7969:Prune2
|
UTSW |
19 |
17,179,034 (GRCm39) |
missense |
probably damaging |
0.98 |
R8092:Prune2
|
UTSW |
19 |
17,097,357 (GRCm39) |
missense |
probably damaging |
1.00 |
R8110:Prune2
|
UTSW |
19 |
17,098,083 (GRCm39) |
missense |
probably benign |
0.22 |
R8115:Prune2
|
UTSW |
19 |
17,101,288 (GRCm39) |
missense |
probably benign |
0.02 |
R8129:Prune2
|
UTSW |
19 |
17,096,200 (GRCm39) |
missense |
probably benign |
0.01 |
R8169:Prune2
|
UTSW |
19 |
17,102,455 (GRCm39) |
missense |
probably benign |
0.10 |
R8171:Prune2
|
UTSW |
19 |
17,097,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R8176:Prune2
|
UTSW |
19 |
17,095,656 (GRCm39) |
missense |
probably damaging |
1.00 |
R8200:Prune2
|
UTSW |
19 |
17,102,337 (GRCm39) |
missense |
probably benign |
0.01 |
R8217:Prune2
|
UTSW |
19 |
17,097,480 (GRCm39) |
missense |
probably benign |
0.01 |
R8258:Prune2
|
UTSW |
19 |
17,189,672 (GRCm39) |
missense |
unknown |
|
R8259:Prune2
|
UTSW |
19 |
17,189,672 (GRCm39) |
missense |
unknown |
|
R8289:Prune2
|
UTSW |
19 |
17,100,373 (GRCm39) |
missense |
probably benign |
0.43 |
R8329:Prune2
|
UTSW |
19 |
17,098,629 (GRCm39) |
missense |
probably benign |
0.02 |
R8342:Prune2
|
UTSW |
19 |
17,103,027 (GRCm39) |
missense |
probably benign |
0.01 |
R8558:Prune2
|
UTSW |
19 |
17,099,602 (GRCm39) |
missense |
probably damaging |
0.98 |
R8732:Prune2
|
UTSW |
19 |
17,097,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R8743:Prune2
|
UTSW |
19 |
17,096,920 (GRCm39) |
missense |
probably benign |
0.22 |
R8769:Prune2
|
UTSW |
19 |
17,100,442 (GRCm39) |
missense |
probably damaging |
0.96 |
R8862:Prune2
|
UTSW |
19 |
17,097,510 (GRCm39) |
missense |
probably benign |
0.04 |
R8936:Prune2
|
UTSW |
19 |
17,099,199 (GRCm39) |
missense |
probably benign |
0.24 |
R9040:Prune2
|
UTSW |
19 |
17,097,991 (GRCm39) |
missense |
probably damaging |
1.00 |
R9084:Prune2
|
UTSW |
19 |
17,097,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R9224:Prune2
|
UTSW |
19 |
17,097,393 (GRCm39) |
missense |
probably damaging |
1.00 |
R9273:Prune2
|
UTSW |
19 |
17,095,690 (GRCm39) |
missense |
possibly damaging |
0.74 |
R9275:Prune2
|
UTSW |
19 |
17,101,144 (GRCm39) |
missense |
probably benign |
0.06 |
R9278:Prune2
|
UTSW |
19 |
17,101,144 (GRCm39) |
missense |
probably benign |
0.06 |
R9290:Prune2
|
UTSW |
19 |
17,145,691 (GRCm39) |
missense |
probably benign |
0.41 |
R9305:Prune2
|
UTSW |
19 |
17,097,625 (GRCm39) |
missense |
probably benign |
0.14 |
R9317:Prune2
|
UTSW |
19 |
17,099,034 (GRCm39) |
missense |
probably benign |
0.00 |
R9354:Prune2
|
UTSW |
19 |
17,099,986 (GRCm39) |
missense |
probably benign |
0.43 |
R9373:Prune2
|
UTSW |
19 |
17,099,502 (GRCm39) |
missense |
probably benign |
|
R9394:Prune2
|
UTSW |
19 |
16,981,053 (GRCm39) |
missense |
probably damaging |
1.00 |
R9405:Prune2
|
UTSW |
19 |
17,193,708 (GRCm39) |
missense |
probably damaging |
0.99 |
R9476:Prune2
|
UTSW |
19 |
17,096,706 (GRCm39) |
missense |
possibly damaging |
0.64 |
R9532:Prune2
|
UTSW |
19 |
17,099,794 (GRCm39) |
missense |
probably benign |
0.00 |
X0019:Prune2
|
UTSW |
19 |
17,098,881 (GRCm39) |
missense |
probably benign |
0.16 |
X0028:Prune2
|
UTSW |
19 |
17,100,249 (GRCm39) |
missense |
probably damaging |
1.00 |
X0064:Prune2
|
UTSW |
19 |
17,099,739 (GRCm39) |
missense |
probably damaging |
1.00 |
X0066:Prune2
|
UTSW |
19 |
17,096,154 (GRCm39) |
missense |
probably damaging |
1.00 |
|