Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017B05Rik |
T |
A |
9: 57,164,468 (GRCm39) |
K635N |
probably damaging |
Het |
Afg3l2 |
G |
T |
18: 67,554,329 (GRCm39) |
L458M |
probably damaging |
Het |
Ahnak |
T |
A |
19: 8,992,705 (GRCm39) |
M4663K |
possibly damaging |
Het |
C4b |
T |
A |
17: 34,960,212 (GRCm39) |
T280S |
probably benign |
Het |
Ccdc166 |
A |
G |
15: 75,852,869 (GRCm39) |
V366A |
probably benign |
Het |
Cdh23 |
A |
G |
10: 60,493,044 (GRCm39) |
|
probably null |
Het |
Col7a1 |
A |
G |
9: 108,792,292 (GRCm39) |
T1281A |
unknown |
Het |
Dbndd1 |
T |
A |
8: 124,233,484 (GRCm39) |
D127V |
probably damaging |
Het |
Ddx20 |
T |
A |
3: 105,590,825 (GRCm39) |
E197V |
probably damaging |
Het |
Dennd10 |
A |
G |
19: 60,814,324 (GRCm39) |
M96V |
probably benign |
Het |
Dnm3 |
A |
G |
1: 161,838,471 (GRCm39) |
S826P |
probably damaging |
Het |
Dnmt3a |
T |
C |
12: 3,945,643 (GRCm39) |
V24A |
probably benign |
Het |
Dop1b |
C |
A |
16: 93,567,392 (GRCm39) |
A1273E |
probably damaging |
Het |
Dsg1c |
T |
C |
18: 20,416,703 (GRCm39) |
V868A |
possibly damaging |
Het |
Dtx4 |
A |
G |
19: 12,462,626 (GRCm39) |
|
probably null |
Het |
Elovl4 |
A |
G |
9: 83,672,154 (GRCm39) |
L55P |
possibly damaging |
Het |
Fbxo40 |
T |
A |
16: 36,789,914 (GRCm39) |
T399S |
possibly damaging |
Het |
Fkbpl |
G |
A |
17: 34,864,303 (GRCm39) |
A24T |
probably benign |
Het |
Gm14399 |
T |
C |
2: 174,973,371 (GRCm39) |
E96G |
probably damaging |
Het |
Gm14496 |
T |
G |
2: 181,642,147 (GRCm39) |
V606G |
probably benign |
Het |
Gpr156 |
A |
G |
16: 37,826,087 (GRCm39) |
E768G |
probably damaging |
Het |
Grm5 |
A |
T |
7: 87,723,704 (GRCm39) |
T665S |
probably damaging |
Het |
Hsdl2 |
A |
G |
4: 59,592,301 (GRCm39) |
|
probably benign |
Het |
Htt |
T |
C |
5: 35,064,928 (GRCm39) |
V3047A |
possibly damaging |
Het |
Igkv3-2 |
A |
T |
6: 70,676,011 (GRCm39) |
T107S |
probably benign |
Het |
Insyn2b |
G |
A |
11: 34,352,788 (GRCm39) |
E277K |
probably damaging |
Het |
Itih2 |
T |
A |
2: 10,101,272 (GRCm39) |
T899S |
probably benign |
Het |
Lhcgr |
T |
A |
17: 89,050,281 (GRCm39) |
Y415F |
probably damaging |
Het |
Ltbr |
G |
A |
6: 125,289,757 (GRCm39) |
R146W |
probably damaging |
Het |
Med4 |
C |
A |
14: 73,747,553 (GRCm39) |
S18* |
probably null |
Het |
Nefl |
T |
C |
14: 68,322,088 (GRCm39) |
V226A |
probably damaging |
Het |
Nploc4 |
T |
A |
11: 120,275,389 (GRCm39) |
N516Y |
probably damaging |
Het |
Or1o4 |
A |
G |
17: 37,590,501 (GRCm39) |
V270A |
probably benign |
Het |
Or6c66 |
A |
T |
10: 129,461,601 (GRCm39) |
F110I |
probably damaging |
Het |
Otx1 |
C |
A |
11: 21,947,037 (GRCm39) |
A91S |
probably damaging |
Het |
Pcdha3 |
T |
G |
18: 37,079,752 (GRCm39) |
L165V |
possibly damaging |
Het |
Pcdhb12 |
T |
A |
18: 37,570,099 (GRCm39) |
V415D |
probably damaging |
Het |
Pcdhga10 |
T |
C |
18: 37,880,503 (GRCm39) |
I88T |
probably damaging |
Het |
Pigyl |
T |
A |
9: 22,069,292 (GRCm39) |
M1K |
probably null |
Het |
Prr27 |
T |
C |
5: 87,991,203 (GRCm39) |
S272P |
probably damaging |
Het |
Prss3 |
C |
T |
6: 41,350,780 (GRCm39) |
D237N |
probably benign |
Het |
Pstpip2 |
A |
G |
18: 77,958,078 (GRCm39) |
D150G |
probably damaging |
Het |
Robo4 |
T |
A |
9: 37,324,674 (GRCm39) |
D909E |
probably benign |
Het |
Serpinb3c |
A |
T |
1: 107,204,661 (GRCm39) |
Y28* |
probably null |
Het |
Slc26a3 |
T |
C |
12: 31,500,980 (GRCm39) |
|
probably null |
Het |
Slc6a1 |
A |
T |
6: 114,279,493 (GRCm39) |
I91F |
probably benign |
Het |
Smcr8 |
T |
G |
11: 60,669,118 (GRCm39) |
Y89D |
probably damaging |
Het |
Sspo |
T |
A |
6: 48,443,247 (GRCm39) |
M1898K |
probably benign |
Het |
Tbl1xr1 |
T |
A |
3: 22,246,233 (GRCm39) |
I251K |
probably damaging |
Het |
Thbs4 |
C |
T |
13: 92,913,501 (GRCm39) |
D140N |
probably benign |
Het |
Tmbim6 |
G |
A |
15: 99,303,633 (GRCm39) |
A108T |
probably benign |
Het |
Trim10 |
T |
G |
17: 37,186,328 (GRCm39) |
L301R |
probably benign |
Het |
Trpm7 |
A |
T |
2: 126,671,161 (GRCm39) |
I607N |
possibly damaging |
Het |
Vmn2r9 |
T |
A |
5: 108,995,929 (GRCm39) |
I240F |
probably damaging |
Het |
Xpot |
T |
A |
10: 121,436,765 (GRCm39) |
I873F |
possibly damaging |
Het |
Zfhx4 |
G |
A |
3: 5,464,267 (GRCm39) |
S1475N |
probably damaging |
Het |
Zfp712 |
A |
G |
13: 67,189,079 (GRCm39) |
S483P |
possibly damaging |
Het |
Zswim7 |
A |
T |
11: 62,158,373 (GRCm39) |
H122Q |
probably benign |
Het |
|
Other mutations in Cul9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00087:Cul9
|
APN |
17 |
46,836,635 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00330:Cul9
|
APN |
17 |
46,821,767 (GRCm39) |
splice site |
probably benign |
|
IGL00726:Cul9
|
APN |
17 |
46,839,022 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01020:Cul9
|
APN |
17 |
46,849,949 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01358:Cul9
|
APN |
17 |
46,849,240 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01410:Cul9
|
APN |
17 |
46,839,572 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01781:Cul9
|
APN |
17 |
46,850,230 (GRCm39) |
missense |
probably benign |
|
IGL01873:Cul9
|
APN |
17 |
46,813,378 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02117:Cul9
|
APN |
17 |
46,851,301 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02300:Cul9
|
APN |
17 |
46,831,958 (GRCm39) |
splice site |
probably benign |
|
IGL02426:Cul9
|
APN |
17 |
46,834,184 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02427:Cul9
|
APN |
17 |
46,813,558 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL02496:Cul9
|
APN |
17 |
46,851,302 (GRCm39) |
missense |
possibly damaging |
0.72 |
IGL03008:Cul9
|
APN |
17 |
46,813,623 (GRCm39) |
splice site |
probably benign |
|
IGL03059:Cul9
|
APN |
17 |
46,849,913 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03302:Cul9
|
APN |
17 |
46,837,566 (GRCm39) |
missense |
probably damaging |
0.98 |
bottlenose
|
UTSW |
17 |
46,811,770 (GRCm39) |
missense |
possibly damaging |
0.79 |
flipper
|
UTSW |
17 |
46,836,818 (GRCm39) |
missense |
probably benign |
0.05 |
orca
|
UTSW |
17 |
46,836,061 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4340:Cul9
|
UTSW |
17 |
46,811,779 (GRCm39) |
small insertion |
probably benign |
|
FR4449:Cul9
|
UTSW |
17 |
46,811,782 (GRCm39) |
small insertion |
probably benign |
|
FR4737:Cul9
|
UTSW |
17 |
46,811,784 (GRCm39) |
small insertion |
probably benign |
|
FR4737:Cul9
|
UTSW |
17 |
46,811,772 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Cul9
|
UTSW |
17 |
46,811,779 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Cul9
|
UTSW |
17 |
46,811,776 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Cul9
|
UTSW |
17 |
46,811,774 (GRCm39) |
small insertion |
probably benign |
|
FR4976:Cul9
|
UTSW |
17 |
46,811,782 (GRCm39) |
small insertion |
probably benign |
|
R0012:Cul9
|
UTSW |
17 |
46,849,436 (GRCm39) |
missense |
probably benign |
0.26 |
R0079:Cul9
|
UTSW |
17 |
46,848,589 (GRCm39) |
nonsense |
probably null |
|
R0143:Cul9
|
UTSW |
17 |
46,837,336 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0390:Cul9
|
UTSW |
17 |
46,839,515 (GRCm39) |
missense |
probably benign |
0.34 |
R0401:Cul9
|
UTSW |
17 |
46,852,630 (GRCm39) |
missense |
probably damaging |
1.00 |
R0529:Cul9
|
UTSW |
17 |
46,831,394 (GRCm39) |
splice site |
probably benign |
|
R0815:Cul9
|
UTSW |
17 |
46,848,748 (GRCm39) |
splice site |
probably null |
|
R0863:Cul9
|
UTSW |
17 |
46,848,748 (GRCm39) |
splice site |
probably null |
|
R0972:Cul9
|
UTSW |
17 |
46,833,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R1173:Cul9
|
UTSW |
17 |
46,833,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R1216:Cul9
|
UTSW |
17 |
46,833,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R1217:Cul9
|
UTSW |
17 |
46,833,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R1261:Cul9
|
UTSW |
17 |
46,836,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R1278:Cul9
|
UTSW |
17 |
46,811,775 (GRCm39) |
small deletion |
probably benign |
|
R1281:Cul9
|
UTSW |
17 |
46,822,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R1349:Cul9
|
UTSW |
17 |
46,833,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R1372:Cul9
|
UTSW |
17 |
46,833,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R1403:Cul9
|
UTSW |
17 |
46,833,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R1403:Cul9
|
UTSW |
17 |
46,833,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R1405:Cul9
|
UTSW |
17 |
46,833,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R1405:Cul9
|
UTSW |
17 |
46,833,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R1467:Cul9
|
UTSW |
17 |
46,836,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R1467:Cul9
|
UTSW |
17 |
46,836,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R1482:Cul9
|
UTSW |
17 |
46,819,473 (GRCm39) |
missense |
probably damaging |
0.99 |
R1491:Cul9
|
UTSW |
17 |
46,849,490 (GRCm39) |
nonsense |
probably null |
|
R1618:Cul9
|
UTSW |
17 |
46,836,818 (GRCm39) |
missense |
probably benign |
0.05 |
R1641:Cul9
|
UTSW |
17 |
46,854,486 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1679:Cul9
|
UTSW |
17 |
46,832,082 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1771:Cul9
|
UTSW |
17 |
46,848,738 (GRCm39) |
missense |
probably benign |
0.41 |
R1803:Cul9
|
UTSW |
17 |
46,814,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R2020:Cul9
|
UTSW |
17 |
46,833,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R2046:Cul9
|
UTSW |
17 |
46,854,659 (GRCm39) |
missense |
probably damaging |
1.00 |
R2056:Cul9
|
UTSW |
17 |
46,854,298 (GRCm39) |
missense |
probably benign |
|
R2088:Cul9
|
UTSW |
17 |
46,837,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R2415:Cul9
|
UTSW |
17 |
46,854,364 (GRCm39) |
missense |
probably benign |
|
R2925:Cul9
|
UTSW |
17 |
46,821,907 (GRCm39) |
missense |
probably benign |
0.08 |
R2964:Cul9
|
UTSW |
17 |
46,813,154 (GRCm39) |
missense |
probably damaging |
0.96 |
R2965:Cul9
|
UTSW |
17 |
46,813,154 (GRCm39) |
missense |
probably damaging |
0.96 |
R3690:Cul9
|
UTSW |
17 |
46,814,957 (GRCm39) |
splice site |
probably null |
|
R3847:Cul9
|
UTSW |
17 |
46,836,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R4437:Cul9
|
UTSW |
17 |
46,813,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R4470:Cul9
|
UTSW |
17 |
46,849,262 (GRCm39) |
missense |
probably benign |
0.00 |
R4540:Cul9
|
UTSW |
17 |
46,814,015 (GRCm39) |
missense |
probably null |
0.98 |
R4555:Cul9
|
UTSW |
17 |
46,812,755 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4604:Cul9
|
UTSW |
17 |
46,841,072 (GRCm39) |
missense |
probably damaging |
0.99 |
R4646:Cul9
|
UTSW |
17 |
46,849,943 (GRCm39) |
nonsense |
probably null |
|
R4799:Cul9
|
UTSW |
17 |
46,811,770 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4822:Cul9
|
UTSW |
17 |
46,840,977 (GRCm39) |
missense |
probably benign |
0.01 |
R4964:Cul9
|
UTSW |
17 |
46,849,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R4965:Cul9
|
UTSW |
17 |
46,849,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R5027:Cul9
|
UTSW |
17 |
46,811,708 (GRCm39) |
missense |
probably damaging |
0.99 |
R5185:Cul9
|
UTSW |
17 |
46,836,758 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5237:Cul9
|
UTSW |
17 |
46,854,393 (GRCm39) |
missense |
probably benign |
0.00 |
R5278:Cul9
|
UTSW |
17 |
46,821,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R5455:Cul9
|
UTSW |
17 |
46,821,772 (GRCm39) |
splice site |
probably null |
|
R5592:Cul9
|
UTSW |
17 |
46,831,517 (GRCm39) |
missense |
probably benign |
0.00 |
R5597:Cul9
|
UTSW |
17 |
46,813,591 (GRCm39) |
missense |
possibly damaging |
0.56 |
R5613:Cul9
|
UTSW |
17 |
46,814,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R6122:Cul9
|
UTSW |
17 |
46,832,854 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6135:Cul9
|
UTSW |
17 |
46,832,379 (GRCm39) |
missense |
probably benign |
|
R6352:Cul9
|
UTSW |
17 |
46,822,241 (GRCm39) |
missense |
probably benign |
0.00 |
R6376:Cul9
|
UTSW |
17 |
46,819,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R6868:Cul9
|
UTSW |
17 |
46,833,109 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6898:Cul9
|
UTSW |
17 |
46,821,952 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7090:Cul9
|
UTSW |
17 |
46,811,765 (GRCm39) |
missense |
probably damaging |
0.96 |
R7193:Cul9
|
UTSW |
17 |
46,849,423 (GRCm39) |
missense |
probably damaging |
0.98 |
R7221:Cul9
|
UTSW |
17 |
46,839,491 (GRCm39) |
missense |
probably damaging |
0.99 |
R7291:Cul9
|
UTSW |
17 |
46,851,359 (GRCm39) |
missense |
probably benign |
0.00 |
R7320:Cul9
|
UTSW |
17 |
46,821,835 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7348:Cul9
|
UTSW |
17 |
46,821,919 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7463:Cul9
|
UTSW |
17 |
46,831,402 (GRCm39) |
splice site |
probably null |
|
R7480:Cul9
|
UTSW |
17 |
46,848,738 (GRCm39) |
missense |
probably benign |
0.41 |
R7573:Cul9
|
UTSW |
17 |
46,830,836 (GRCm39) |
missense |
probably benign |
|
R7582:Cul9
|
UTSW |
17 |
46,821,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R7605:Cul9
|
UTSW |
17 |
46,852,658 (GRCm39) |
missense |
probably damaging |
0.99 |
R7684:Cul9
|
UTSW |
17 |
46,820,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R7830:Cul9
|
UTSW |
17 |
46,851,237 (GRCm39) |
missense |
probably benign |
0.37 |
R7834:Cul9
|
UTSW |
17 |
46,836,630 (GRCm39) |
splice site |
probably null |
|
R8131:Cul9
|
UTSW |
17 |
46,822,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R8192:Cul9
|
UTSW |
17 |
46,849,273 (GRCm39) |
missense |
probably benign |
0.01 |
R8231:Cul9
|
UTSW |
17 |
46,831,427 (GRCm39) |
missense |
probably damaging |
0.99 |
R8248:Cul9
|
UTSW |
17 |
46,840,940 (GRCm39) |
missense |
probably damaging |
0.99 |
R8504:Cul9
|
UTSW |
17 |
46,814,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R8550:Cul9
|
UTSW |
17 |
46,830,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R8716:Cul9
|
UTSW |
17 |
46,838,840 (GRCm39) |
missense |
probably benign |
0.28 |
R8769:Cul9
|
UTSW |
17 |
46,832,828 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8893:Cul9
|
UTSW |
17 |
46,811,775 (GRCm39) |
small deletion |
probably benign |
|
R8904:Cul9
|
UTSW |
17 |
46,831,427 (GRCm39) |
missense |
probably damaging |
0.99 |
R8936:Cul9
|
UTSW |
17 |
46,839,528 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8972:Cul9
|
UTSW |
17 |
46,854,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R9003:Cul9
|
UTSW |
17 |
46,836,001 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9012:Cul9
|
UTSW |
17 |
46,854,447 (GRCm39) |
missense |
probably benign |
|
R9056:Cul9
|
UTSW |
17 |
46,854,696 (GRCm39) |
missense |
probably damaging |
0.99 |
R9071:Cul9
|
UTSW |
17 |
46,837,379 (GRCm39) |
missense |
probably benign |
|
R9162:Cul9
|
UTSW |
17 |
46,837,529 (GRCm39) |
missense |
probably benign |
0.32 |
R9476:Cul9
|
UTSW |
17 |
46,821,833 (GRCm39) |
missense |
probably damaging |
1.00 |
R9526:Cul9
|
UTSW |
17 |
46,841,026 (GRCm39) |
missense |
probably benign |
0.41 |
R9563:Cul9
|
UTSW |
17 |
46,820,897 (GRCm39) |
missense |
probably benign |
0.01 |
R9568:Cul9
|
UTSW |
17 |
46,831,044 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9610:Cul9
|
UTSW |
17 |
46,830,823 (GRCm39) |
missense |
possibly damaging |
0.96 |
R9611:Cul9
|
UTSW |
17 |
46,830,823 (GRCm39) |
missense |
possibly damaging |
0.96 |
R9705:Cul9
|
UTSW |
17 |
46,854,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R9765:Cul9
|
UTSW |
17 |
46,850,224 (GRCm39) |
missense |
probably benign |
0.18 |
RF011:Cul9
|
UTSW |
17 |
46,811,774 (GRCm39) |
small insertion |
probably benign |
|
RF016:Cul9
|
UTSW |
17 |
46,811,789 (GRCm39) |
nonsense |
probably null |
|
RF026:Cul9
|
UTSW |
17 |
46,811,795 (GRCm39) |
nonsense |
probably null |
|
RF027:Cul9
|
UTSW |
17 |
46,811,774 (GRCm39) |
small insertion |
probably benign |
|
RF030:Cul9
|
UTSW |
17 |
46,811,795 (GRCm39) |
small insertion |
probably benign |
|
RF033:Cul9
|
UTSW |
17 |
46,811,780 (GRCm39) |
small insertion |
probably benign |
|
RF039:Cul9
|
UTSW |
17 |
46,811,780 (GRCm39) |
small insertion |
probably benign |
|
RF041:Cul9
|
UTSW |
17 |
46,811,780 (GRCm39) |
nonsense |
probably null |
|
RF042:Cul9
|
UTSW |
17 |
46,851,541 (GRCm39) |
frame shift |
probably null |
|
RF057:Cul9
|
UTSW |
17 |
46,811,789 (GRCm39) |
nonsense |
probably null |
|
Z1176:Cul9
|
UTSW |
17 |
46,831,511 (GRCm39) |
nonsense |
probably null |
|
Z1176:Cul9
|
UTSW |
17 |
46,831,502 (GRCm39) |
nonsense |
probably null |
|
Z1177:Cul9
|
UTSW |
17 |
46,848,723 (GRCm39) |
missense |
probably benign |
0.14 |
|