Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8a |
A |
T |
11: 109,982,420 (GRCm39) |
N7K |
probably benign |
Het |
Akap9 |
T |
A |
5: 4,111,183 (GRCm39) |
D3081E |
probably benign |
Het |
Amer2 |
G |
A |
14: 60,616,854 (GRCm39) |
A350T |
probably damaging |
Het |
Amotl1 |
A |
G |
9: 14,466,868 (GRCm39) |
|
probably null |
Het |
Ankib1 |
A |
T |
5: 3,752,995 (GRCm39) |
V651E |
probably damaging |
Het |
Aox1 |
T |
C |
1: 58,115,283 (GRCm39) |
V756A |
probably damaging |
Het |
Arap2 |
A |
C |
5: 62,887,954 (GRCm39) |
I464S |
probably benign |
Het |
Atp8a2 |
A |
C |
14: 60,263,657 (GRCm39) |
M359R |
probably damaging |
Het |
Aunip |
T |
C |
4: 134,250,618 (GRCm39) |
S188P |
possibly damaging |
Het |
Cdt1 |
A |
G |
8: 123,298,728 (GRCm39) |
E455G |
probably benign |
Het |
Cyp2r1 |
G |
T |
7: 114,149,590 (GRCm39) |
H475N |
probably benign |
Het |
Dnah7a |
G |
T |
1: 53,543,049 (GRCm39) |
H2374N |
probably benign |
Het |
Dsc2 |
C |
T |
18: 20,165,331 (GRCm39) |
G881R |
possibly damaging |
Het |
Dst |
G |
A |
1: 34,313,261 (GRCm39) |
A4343T |
probably benign |
Het |
Efcab3 |
A |
G |
11: 105,002,677 (GRCm39) |
D304G |
possibly damaging |
Het |
Efcc1 |
T |
C |
6: 87,728,772 (GRCm39) |
L409P |
probably damaging |
Het |
Eno1 |
G |
T |
4: 150,325,526 (GRCm39) |
S37I |
probably damaging |
Het |
Ermp1 |
A |
T |
19: 29,601,196 (GRCm39) |
L517Q |
probably damaging |
Het |
Farp1 |
T |
G |
14: 121,471,232 (GRCm39) |
I196S |
probably damaging |
Het |
Fbxo21 |
A |
G |
5: 118,128,919 (GRCm39) |
T310A |
possibly damaging |
Het |
Fbxo31 |
C |
T |
8: 122,287,127 (GRCm39) |
V149M |
probably damaging |
Het |
Ggcx |
C |
A |
6: 72,406,511 (GRCm39) |
T658N |
possibly damaging |
Het |
Gpc5 |
A |
C |
14: 115,636,637 (GRCm39) |
H440P |
probably damaging |
Het |
H13 |
C |
T |
2: 152,537,446 (GRCm39) |
A297V |
probably damaging |
Het |
H2-DMb1 |
T |
A |
17: 34,374,443 (GRCm39) |
L31Q |
probably damaging |
Het |
Ifi207 |
G |
A |
1: 173,557,746 (GRCm39) |
P331S |
unknown |
Het |
Il11ra1 |
G |
T |
4: 41,766,251 (GRCm39) |
A263S |
probably benign |
Het |
Il1a |
C |
A |
2: 129,144,864 (GRCm39) |
V185F |
probably damaging |
Het |
Ippk |
C |
T |
13: 49,599,818 (GRCm39) |
P226S |
|
Het |
Kdm4d |
T |
A |
9: 14,375,237 (GRCm39) |
K207M |
probably damaging |
Het |
Lrrc37 |
A |
T |
11: 103,434,115 (GRCm39) |
M3018K |
unknown |
Het |
Lrrc4b |
T |
C |
7: 44,110,533 (GRCm39) |
L135P |
probably damaging |
Het |
Lrrk1 |
A |
G |
7: 65,912,371 (GRCm39) |
Y1730H |
possibly damaging |
Het |
Mcpt2 |
C |
A |
14: 56,279,663 (GRCm39) |
A18D |
probably damaging |
Het |
Mtmr4 |
C |
T |
11: 87,502,756 (GRCm39) |
R937* |
probably null |
Het |
Muc16 |
T |
A |
9: 18,570,033 (GRCm39) |
T829S |
unknown |
Het |
Myof |
A |
C |
19: 37,921,167 (GRCm39) |
I1365S |
probably damaging |
Het |
Npc2 |
C |
T |
12: 84,807,612 (GRCm39) |
R82Q |
probably benign |
Het |
Or10ag2 |
T |
A |
2: 87,249,081 (GRCm39) |
S228T |
probably damaging |
Het |
Or10d1c |
A |
T |
9: 38,894,169 (GRCm39) |
M57K |
probably damaging |
Het |
Or10j2 |
T |
A |
1: 173,098,047 (GRCm39) |
F102I |
possibly damaging |
Het |
Or2g25 |
G |
A |
17: 37,970,631 (GRCm39) |
L198F |
probably damaging |
Het |
Or4k45 |
T |
C |
2: 111,395,783 (GRCm39) |
D2G |
probably benign |
Het |
Or8b3b |
A |
T |
9: 38,584,464 (GRCm39) |
I92N |
possibly damaging |
Het |
Or8d2b |
T |
A |
9: 38,789,026 (GRCm39) |
S185T |
probably damaging |
Het |
Pdzph1 |
T |
C |
17: 59,282,138 (GRCm39) |
N48S |
probably benign |
Het |
Plce1 |
A |
T |
19: 38,513,262 (GRCm39) |
H187L |
probably benign |
Het |
Pramel6 |
G |
T |
2: 87,338,808 (GRCm39) |
V3F |
probably benign |
Het |
Prr5l |
CCTCGCTCGCTCGCTCGC |
CCTCGCTCGCTCGC |
2: 101,627,919 (GRCm39) |
|
probably null |
Het |
Pwwp3a |
G |
A |
10: 80,076,231 (GRCm39) |
G474S |
probably damaging |
Het |
Rabgap1l |
A |
G |
1: 160,530,012 (GRCm39) |
Y358H |
probably benign |
Het |
Rbbp8 |
T |
C |
18: 11,855,727 (GRCm39) |
S625P |
probably damaging |
Het |
Rhot1 |
A |
T |
11: 80,141,879 (GRCm39) |
K461I |
probably benign |
Het |
Rpa1 |
G |
A |
11: 75,193,501 (GRCm39) |
T610I |
possibly damaging |
Het |
Ryr1 |
G |
T |
7: 28,810,308 (GRCm39) |
H316N |
probably benign |
Het |
Shprh |
T |
C |
10: 11,089,205 (GRCm39) |
S1648P |
probably damaging |
Het |
Sipa1 |
A |
T |
19: 5,702,140 (GRCm39) |
D923E |
possibly damaging |
Het |
Spata6 |
A |
G |
4: 111,685,517 (GRCm39) |
Y474C |
possibly damaging |
Het |
Sptbn1 |
A |
T |
11: 30,089,117 (GRCm39) |
I715N |
probably damaging |
Het |
Stard9 |
T |
A |
2: 120,495,420 (GRCm39) |
C98* |
probably null |
Het |
Tfpi2 |
T |
C |
6: 3,963,872 (GRCm39) |
T187A |
probably damaging |
Het |
Tmem63a |
G |
T |
1: 180,788,048 (GRCm39) |
K267N |
probably benign |
Het |
Topaz1 |
C |
T |
9: 122,604,708 (GRCm39) |
A1104V |
probably benign |
Het |
Trmt11 |
A |
G |
10: 30,442,490 (GRCm39) |
I231T |
possibly damaging |
Het |
Utp15 |
G |
A |
13: 98,387,371 (GRCm39) |
T401I |
probably benign |
Het |
Vmn2r13 |
T |
C |
5: 109,322,926 (GRCm39) |
K121R |
probably benign |
Het |
Xab2 |
C |
T |
8: 3,663,830 (GRCm39) |
R363H |
probably damaging |
Het |
Zfand2b |
T |
A |
1: 75,145,504 (GRCm39) |
F3L |
possibly damaging |
Het |
Zfyve28 |
A |
T |
5: 34,374,944 (GRCm39) |
S357T |
probably damaging |
Het |
|
Other mutations in Stab1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00087:Stab1
|
APN |
14 |
30,883,314 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00323:Stab1
|
APN |
14 |
30,861,263 (GRCm39) |
missense |
probably benign |
0.04 |
IGL00515:Stab1
|
APN |
14 |
30,881,686 (GRCm39) |
missense |
probably benign |
0.20 |
IGL00844:Stab1
|
APN |
14 |
30,869,023 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01374:Stab1
|
APN |
14 |
30,869,032 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01384:Stab1
|
APN |
14 |
30,872,365 (GRCm39) |
missense |
probably benign |
|
IGL01431:Stab1
|
APN |
14 |
30,870,952 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01787:Stab1
|
APN |
14 |
30,861,765 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02128:Stab1
|
APN |
14 |
30,872,398 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02138:Stab1
|
APN |
14 |
30,865,470 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02256:Stab1
|
APN |
14 |
30,863,549 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02340:Stab1
|
APN |
14 |
30,862,367 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02507:Stab1
|
APN |
14 |
30,861,167 (GRCm39) |
unclassified |
probably benign |
|
IGL02695:Stab1
|
APN |
14 |
30,881,228 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02755:Stab1
|
APN |
14 |
30,861,595 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02870:Stab1
|
APN |
14 |
30,861,354 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02884:Stab1
|
APN |
14 |
30,872,100 (GRCm39) |
splice site |
probably null |
|
IGL03035:Stab1
|
APN |
14 |
30,869,726 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03267:Stab1
|
APN |
14 |
30,864,686 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03286:Stab1
|
APN |
14 |
30,881,283 (GRCm39) |
splice site |
probably benign |
|
IGL03366:Stab1
|
APN |
14 |
30,872,220 (GRCm39) |
missense |
possibly damaging |
0.58 |
IGL03412:Stab1
|
APN |
14 |
30,876,364 (GRCm39) |
missense |
probably benign |
0.42 |
R0906_Stab1_335
|
UTSW |
14 |
30,867,206 (GRCm39) |
missense |
probably benign |
0.19 |
R5086_Stab1_467
|
UTSW |
14 |
30,881,261 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02835:Stab1
|
UTSW |
14 |
30,867,981 (GRCm39) |
critical splice donor site |
probably null |
|
K7371:Stab1
|
UTSW |
14 |
30,872,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R0053:Stab1
|
UTSW |
14 |
30,862,644 (GRCm39) |
missense |
possibly damaging |
0.57 |
R0053:Stab1
|
UTSW |
14 |
30,862,644 (GRCm39) |
missense |
possibly damaging |
0.57 |
R0066:Stab1
|
UTSW |
14 |
30,879,027 (GRCm39) |
splice site |
probably benign |
|
R0066:Stab1
|
UTSW |
14 |
30,879,027 (GRCm39) |
splice site |
probably benign |
|
R0363:Stab1
|
UTSW |
14 |
30,880,965 (GRCm39) |
splice site |
probably benign |
|
R0387:Stab1
|
UTSW |
14 |
30,870,058 (GRCm39) |
missense |
probably benign |
0.00 |
R0391:Stab1
|
UTSW |
14 |
30,865,375 (GRCm39) |
missense |
probably benign |
0.21 |
R0513:Stab1
|
UTSW |
14 |
30,870,902 (GRCm39) |
missense |
probably benign |
0.08 |
R0546:Stab1
|
UTSW |
14 |
30,861,507 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0825:Stab1
|
UTSW |
14 |
30,874,557 (GRCm39) |
missense |
probably benign |
0.16 |
R0906:Stab1
|
UTSW |
14 |
30,867,206 (GRCm39) |
missense |
probably benign |
0.19 |
R0963:Stab1
|
UTSW |
14 |
30,869,231 (GRCm39) |
missense |
probably damaging |
0.97 |
R1219:Stab1
|
UTSW |
14 |
30,862,578 (GRCm39) |
splice site |
probably null |
|
R1234:Stab1
|
UTSW |
14 |
30,872,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R1260:Stab1
|
UTSW |
14 |
30,873,846 (GRCm39) |
missense |
probably damaging |
1.00 |
R1400:Stab1
|
UTSW |
14 |
30,861,787 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1405:Stab1
|
UTSW |
14 |
30,870,958 (GRCm39) |
missense |
probably benign |
0.19 |
R1405:Stab1
|
UTSW |
14 |
30,870,958 (GRCm39) |
missense |
probably benign |
0.19 |
R1440:Stab1
|
UTSW |
14 |
30,873,647 (GRCm39) |
nonsense |
probably null |
|
R1472:Stab1
|
UTSW |
14 |
30,863,543 (GRCm39) |
missense |
probably benign |
0.01 |
R1474:Stab1
|
UTSW |
14 |
30,871,818 (GRCm39) |
missense |
probably benign |
0.45 |
R1475:Stab1
|
UTSW |
14 |
30,885,785 (GRCm39) |
missense |
probably benign |
|
R1509:Stab1
|
UTSW |
14 |
30,873,541 (GRCm39) |
splice site |
probably benign |
|
R1551:Stab1
|
UTSW |
14 |
30,882,456 (GRCm39) |
missense |
probably benign |
0.00 |
R1572:Stab1
|
UTSW |
14 |
30,872,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R1633:Stab1
|
UTSW |
14 |
30,872,337 (GRCm39) |
splice site |
probably null |
|
R1719:Stab1
|
UTSW |
14 |
30,867,985 (GRCm39) |
nonsense |
probably null |
|
R1733:Stab1
|
UTSW |
14 |
30,867,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R1763:Stab1
|
UTSW |
14 |
30,890,373 (GRCm39) |
missense |
probably benign |
0.04 |
R1808:Stab1
|
UTSW |
14 |
30,863,101 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1816:Stab1
|
UTSW |
14 |
30,879,422 (GRCm39) |
missense |
probably benign |
0.03 |
R1853:Stab1
|
UTSW |
14 |
30,862,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R1891:Stab1
|
UTSW |
14 |
30,863,287 (GRCm39) |
missense |
probably benign |
0.07 |
R1984:Stab1
|
UTSW |
14 |
30,872,605 (GRCm39) |
missense |
probably benign |
0.20 |
R1998:Stab1
|
UTSW |
14 |
30,884,110 (GRCm39) |
nonsense |
probably null |
|
R2165:Stab1
|
UTSW |
14 |
30,890,392 (GRCm39) |
missense |
probably benign |
0.20 |
R2191:Stab1
|
UTSW |
14 |
30,881,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R2191:Stab1
|
UTSW |
14 |
30,864,757 (GRCm39) |
missense |
probably benign |
0.03 |
R2233:Stab1
|
UTSW |
14 |
30,883,837 (GRCm39) |
missense |
probably benign |
0.08 |
R2303:Stab1
|
UTSW |
14 |
30,868,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R2496:Stab1
|
UTSW |
14 |
30,883,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R2504:Stab1
|
UTSW |
14 |
30,884,997 (GRCm39) |
critical splice donor site |
probably null |
|
R2519:Stab1
|
UTSW |
14 |
30,876,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R2926:Stab1
|
UTSW |
14 |
30,883,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R4025:Stab1
|
UTSW |
14 |
30,876,909 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4113:Stab1
|
UTSW |
14 |
30,890,436 (GRCm39) |
missense |
probably damaging |
0.98 |
R4258:Stab1
|
UTSW |
14 |
30,876,629 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4588:Stab1
|
UTSW |
14 |
30,879,402 (GRCm39) |
missense |
probably benign |
0.01 |
R4644:Stab1
|
UTSW |
14 |
30,862,444 (GRCm39) |
unclassified |
probably benign |
|
R4660:Stab1
|
UTSW |
14 |
30,876,872 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4801:Stab1
|
UTSW |
14 |
30,863,328 (GRCm39) |
nonsense |
probably null |
|
R4802:Stab1
|
UTSW |
14 |
30,863,328 (GRCm39) |
nonsense |
probably null |
|
R4870:Stab1
|
UTSW |
14 |
30,864,000 (GRCm39) |
missense |
probably benign |
0.13 |
R4872:Stab1
|
UTSW |
14 |
30,862,350 (GRCm39) |
missense |
probably damaging |
1.00 |
R4881:Stab1
|
UTSW |
14 |
30,865,629 (GRCm39) |
missense |
probably benign |
0.32 |
R4941:Stab1
|
UTSW |
14 |
30,873,528 (GRCm39) |
missense |
probably benign |
0.00 |
R5061:Stab1
|
UTSW |
14 |
30,885,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R5086:Stab1
|
UTSW |
14 |
30,881,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R5086:Stab1
|
UTSW |
14 |
30,865,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R5087:Stab1
|
UTSW |
14 |
30,881,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R5092:Stab1
|
UTSW |
14 |
30,867,812 (GRCm39) |
missense |
probably benign |
0.01 |
R5102:Stab1
|
UTSW |
14 |
30,869,974 (GRCm39) |
critical splice donor site |
probably null |
|
R5107:Stab1
|
UTSW |
14 |
30,885,752 (GRCm39) |
splice site |
probably null |
|
R5195:Stab1
|
UTSW |
14 |
30,862,478 (GRCm39) |
unclassified |
probably benign |
|
R5217:Stab1
|
UTSW |
14 |
30,881,476 (GRCm39) |
missense |
probably benign |
0.25 |
R5285:Stab1
|
UTSW |
14 |
30,865,433 (GRCm39) |
unclassified |
probably benign |
|
R5327:Stab1
|
UTSW |
14 |
30,883,793 (GRCm39) |
nonsense |
probably null |
|
R5647:Stab1
|
UTSW |
14 |
30,879,397 (GRCm39) |
nonsense |
probably null |
|
R5696:Stab1
|
UTSW |
14 |
30,882,178 (GRCm39) |
missense |
probably benign |
|
R5996:Stab1
|
UTSW |
14 |
30,861,508 (GRCm39) |
missense |
probably benign |
0.39 |
R6016:Stab1
|
UTSW |
14 |
30,880,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R6017:Stab1
|
UTSW |
14 |
30,863,501 (GRCm39) |
missense |
probably benign |
0.00 |
R6174:Stab1
|
UTSW |
14 |
30,884,476 (GRCm39) |
nonsense |
probably null |
|
R6366:Stab1
|
UTSW |
14 |
30,863,395 (GRCm39) |
missense |
probably benign |
0.10 |
R6754:Stab1
|
UTSW |
14 |
30,863,038 (GRCm39) |
missense |
probably benign |
|
R6788:Stab1
|
UTSW |
14 |
30,861,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R6898:Stab1
|
UTSW |
14 |
30,880,920 (GRCm39) |
missense |
probably benign |
0.00 |
R7124:Stab1
|
UTSW |
14 |
30,882,824 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7145:Stab1
|
UTSW |
14 |
30,867,030 (GRCm39) |
critical splice donor site |
probably null |
|
R7153:Stab1
|
UTSW |
14 |
30,882,541 (GRCm39) |
missense |
probably benign |
0.16 |
R7213:Stab1
|
UTSW |
14 |
30,865,630 (GRCm39) |
missense |
probably benign |
|
R7215:Stab1
|
UTSW |
14 |
30,882,754 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7319:Stab1
|
UTSW |
14 |
30,862,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R7389:Stab1
|
UTSW |
14 |
30,869,196 (GRCm39) |
missense |
probably benign |
0.00 |
R7400:Stab1
|
UTSW |
14 |
30,879,341 (GRCm39) |
missense |
probably null |
1.00 |
R7427:Stab1
|
UTSW |
14 |
30,881,216 (GRCm39) |
missense |
probably benign |
0.00 |
R7428:Stab1
|
UTSW |
14 |
30,881,216 (GRCm39) |
missense |
probably benign |
0.00 |
R7484:Stab1
|
UTSW |
14 |
30,882,274 (GRCm39) |
missense |
probably benign |
0.00 |
R7568:Stab1
|
UTSW |
14 |
30,874,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R7574:Stab1
|
UTSW |
14 |
30,876,622 (GRCm39) |
missense |
probably benign |
|
R7619:Stab1
|
UTSW |
14 |
30,867,194 (GRCm39) |
missense |
probably benign |
|
R7623:Stab1
|
UTSW |
14 |
30,862,578 (GRCm39) |
missense |
probably benign |
0.03 |
R7721:Stab1
|
UTSW |
14 |
30,863,413 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7869:Stab1
|
UTSW |
14 |
30,876,429 (GRCm39) |
missense |
probably benign |
0.01 |
R7936:Stab1
|
UTSW |
14 |
30,879,372 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7956:Stab1
|
UTSW |
14 |
30,881,981 (GRCm39) |
missense |
probably benign |
0.02 |
R7973:Stab1
|
UTSW |
14 |
30,881,590 (GRCm39) |
critical splice donor site |
probably null |
|
R8059:Stab1
|
UTSW |
14 |
30,882,198 (GRCm39) |
missense |
probably benign |
0.02 |
R8304:Stab1
|
UTSW |
14 |
30,870,911 (GRCm39) |
missense |
probably benign |
0.14 |
R8368:Stab1
|
UTSW |
14 |
30,870,368 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8495:Stab1
|
UTSW |
14 |
30,877,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R8513:Stab1
|
UTSW |
14 |
30,871,747 (GRCm39) |
critical splice donor site |
probably null |
|
R8544:Stab1
|
UTSW |
14 |
30,885,008 (GRCm39) |
nonsense |
probably null |
|
R8671:Stab1
|
UTSW |
14 |
30,879,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R8885:Stab1
|
UTSW |
14 |
30,883,771 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8974:Stab1
|
UTSW |
14 |
30,882,779 (GRCm39) |
missense |
probably benign |
|
R9022:Stab1
|
UTSW |
14 |
30,882,226 (GRCm39) |
missense |
probably benign |
0.01 |
R9059:Stab1
|
UTSW |
14 |
30,876,805 (GRCm39) |
missense |
probably benign |
0.01 |
R9226:Stab1
|
UTSW |
14 |
30,867,812 (GRCm39) |
missense |
probably benign |
0.00 |
R9272:Stab1
|
UTSW |
14 |
30,867,298 (GRCm39) |
missense |
probably benign |
0.05 |
R9388:Stab1
|
UTSW |
14 |
30,876,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R9401:Stab1
|
UTSW |
14 |
30,883,069 (GRCm39) |
missense |
probably benign |
|
R9433:Stab1
|
UTSW |
14 |
30,865,531 (GRCm39) |
missense |
probably benign |
0.00 |
R9450:Stab1
|
UTSW |
14 |
30,884,896 (GRCm39) |
missense |
possibly damaging |
0.62 |
R9505:Stab1
|
UTSW |
14 |
30,877,722 (GRCm39) |
missense |
probably damaging |
1.00 |
R9570:Stab1
|
UTSW |
14 |
30,864,638 (GRCm39) |
missense |
probably benign |
0.01 |
R9624:Stab1
|
UTSW |
14 |
30,863,345 (GRCm39) |
missense |
|
|
R9694:Stab1
|
UTSW |
14 |
30,876,901 (GRCm39) |
missense |
probably benign |
0.06 |
R9723:Stab1
|
UTSW |
14 |
30,885,848 (GRCm39) |
missense |
probably benign |
0.10 |
X0026:Stab1
|
UTSW |
14 |
30,884,148 (GRCm39) |
missense |
possibly damaging |
0.91 |
Z1176:Stab1
|
UTSW |
14 |
30,872,617 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Stab1
|
UTSW |
14 |
30,863,995 (GRCm39) |
missense |
probably benign |
0.00 |
|