Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5730409E04Rik |
A |
G |
4: 126,506,104 (GRCm39) |
K211E |
probably damaging |
Het |
Acot7 |
A |
G |
4: 152,291,285 (GRCm39) |
I84V |
possibly damaging |
Het |
Ankrd44 |
A |
G |
1: 54,867,781 (GRCm39) |
V34A |
probably benign |
Het |
Atp4b |
A |
T |
8: 13,443,489 (GRCm39) |
M63K |
probably damaging |
Het |
Atr |
T |
A |
9: 95,818,516 (GRCm39) |
I2163K |
probably damaging |
Het |
Azgp1 |
A |
T |
5: 137,983,426 (GRCm39) |
R34* |
probably null |
Het |
Ccdc152 |
T |
G |
15: 3,327,603 (GRCm39) |
K58T |
probably damaging |
Het |
Ccdc88b |
T |
A |
19: 6,827,837 (GRCm39) |
Q912L |
probably benign |
Het |
Cdc42ep5 |
T |
A |
7: 4,154,395 (GRCm39) |
H131L |
probably benign |
Het |
Chd7 |
G |
A |
4: 8,844,675 (GRCm39) |
E1595K |
probably damaging |
Het |
Col11a1 |
G |
A |
3: 113,925,290 (GRCm39) |
G41D |
probably damaging |
Het |
Cyp2b23 |
C |
T |
7: 26,385,843 (GRCm39) |
V5I |
probably benign |
Het |
D430041D05Rik |
A |
G |
2: 104,085,915 (GRCm39) |
V22A |
possibly damaging |
Het |
Ddi1 |
T |
C |
9: 6,266,012 (GRCm39) |
Y119C |
probably benign |
Het |
Dysf |
T |
C |
6: 84,083,923 (GRCm39) |
L785P |
probably damaging |
Het |
Eqtn |
T |
A |
4: 94,816,587 (GRCm39) |
T69S |
possibly damaging |
Het |
F11 |
T |
A |
8: 45,694,617 (GRCm39) |
K581N |
probably damaging |
Het |
Gli2 |
G |
A |
1: 118,782,290 (GRCm39) |
P172S |
probably damaging |
Het |
Gm7579 |
G |
T |
7: 141,765,603 (GRCm39) |
C3F |
unknown |
Het |
Grin2a |
A |
G |
16: 9,481,194 (GRCm39) |
V501A |
possibly damaging |
Het |
Grk4 |
G |
A |
5: 34,831,901 (GRCm39) |
D57N |
probably damaging |
Het |
Gsdma |
A |
T |
11: 98,557,319 (GRCm39) |
D86V |
probably damaging |
Het |
Gsx1 |
A |
G |
5: 147,126,738 (GRCm39) |
E187G |
probably damaging |
Het |
Hdac1-ps |
A |
G |
17: 78,799,537 (GRCm39) |
D176G |
probably damaging |
Het |
Inpp5k |
T |
A |
11: 75,524,307 (GRCm39) |
F75L |
probably benign |
Het |
Itpr1 |
T |
C |
6: 108,326,620 (GRCm39) |
V114A |
possibly damaging |
Het |
Izumo3 |
A |
T |
4: 92,032,977 (GRCm39) |
C130S |
probably damaging |
Het |
Mei4 |
G |
A |
9: 81,809,639 (GRCm39) |
E241K |
possibly damaging |
Het |
Mocs2 |
T |
C |
13: 114,961,120 (GRCm39) |
V39A |
probably benign |
Het |
Mroh2b |
G |
A |
15: 4,974,572 (GRCm39) |
R1184H |
probably benign |
Het |
Msh3 |
T |
C |
13: 92,436,783 (GRCm39) |
Q509R |
probably null |
Het |
Myh8 |
T |
C |
11: 67,192,497 (GRCm39) |
W1459R |
probably damaging |
Het |
Mypop |
T |
A |
7: 18,734,918 (GRCm39) |
|
probably benign |
Het |
Ndc1 |
C |
A |
4: 107,225,293 (GRCm39) |
T3K |
probably damaging |
Het |
Nf1 |
A |
C |
11: 79,331,749 (GRCm39) |
M695L |
probably benign |
Het |
Nup50l |
A |
G |
6: 96,141,793 (GRCm39) |
M417T |
probably benign |
Het |
Nutm2 |
C |
A |
13: 50,623,955 (GRCm39) |
D217E |
possibly damaging |
Het |
Or52a20 |
T |
C |
7: 103,365,858 (GRCm39) |
I19T |
probably damaging |
Het |
Or5b122 |
A |
G |
19: 13,562,994 (GRCm39) |
T109A |
probably benign |
Het |
Pde6c |
C |
A |
19: 38,129,940 (GRCm39) |
D283E |
probably damaging |
Het |
Phldb2 |
A |
G |
16: 45,591,142 (GRCm39) |
|
probably benign |
Het |
Pigt |
G |
C |
2: 164,349,419 (GRCm39) |
R574P |
probably damaging |
Het |
Pkd1 |
T |
C |
17: 24,796,500 (GRCm39) |
I2354T |
possibly damaging |
Het |
Prdm15 |
T |
C |
16: 97,640,506 (GRCm39) |
E27G |
probably damaging |
Het |
Ptpn14 |
A |
G |
1: 189,597,709 (GRCm39) |
I1140V |
probably benign |
Het |
Rdx |
T |
C |
9: 51,974,891 (GRCm39) |
V9A |
probably damaging |
Het |
Rfx7 |
T |
C |
9: 72,519,071 (GRCm39) |
S258P |
probably damaging |
Het |
Rnf17 |
G |
T |
14: 56,730,822 (GRCm39) |
G1209C |
probably damaging |
Het |
S1pr4 |
C |
T |
10: 81,335,225 (GRCm39) |
|
probably null |
Het |
Scml2 |
G |
T |
X: 160,014,442 (GRCm39) |
E566D |
possibly damaging |
Het |
Serpinb1b |
T |
A |
13: 33,277,646 (GRCm39) |
V293E |
possibly damaging |
Het |
Serpinb9b |
T |
C |
13: 33,222,112 (GRCm39) |
|
probably null |
Het |
Sez6l |
A |
C |
5: 112,622,915 (GRCm39) |
I212S |
probably damaging |
Het |
Spag9 |
G |
A |
11: 93,939,365 (GRCm39) |
R98H |
probably damaging |
Het |
Spata31e2 |
A |
T |
1: 26,723,511 (GRCm39) |
H556Q |
possibly damaging |
Het |
St3gal5 |
T |
C |
6: 72,119,272 (GRCm39) |
L128P |
probably benign |
Het |
Stra6 |
A |
T |
9: 58,059,166 (GRCm39) |
M510L |
probably benign |
Het |
Stxbp5l |
A |
G |
16: 37,028,473 (GRCm39) |
V530A |
probably benign |
Het |
Tatdn1 |
A |
G |
15: 58,793,039 (GRCm39) |
|
probably benign |
Het |
Tbc1d8 |
A |
G |
1: 39,430,206 (GRCm39) |
S466P |
probably benign |
Het |
Tmem199 |
A |
T |
11: 78,399,152 (GRCm39) |
M175K |
possibly damaging |
Het |
Trmt12 |
A |
G |
15: 58,744,764 (GRCm39) |
E54G |
probably benign |
Het |
Usp37 |
G |
T |
1: 74,532,163 (GRCm39) |
Q77K |
possibly damaging |
Het |
Vezf1 |
A |
G |
11: 87,967,125 (GRCm39) |
I301V |
possibly damaging |
Het |
Vmn1r34 |
T |
G |
6: 66,613,932 (GRCm39) |
M269L |
probably benign |
Het |
Wdr93 |
C |
A |
7: 79,421,257 (GRCm39) |
|
probably null |
Het |
Wnk2 |
T |
C |
13: 49,214,370 (GRCm39) |
D644G |
probably damaging |
Het |
Zc3h13 |
C |
T |
14: 75,574,923 (GRCm39) |
R1591* |
probably null |
Het |
Zfp131 |
G |
A |
13: 120,230,316 (GRCm39) |
L371F |
probably damaging |
Het |
Zfp180 |
T |
A |
7: 23,804,049 (GRCm39) |
V156D |
probably benign |
Het |
Zfp646 |
G |
T |
7: 127,479,359 (GRCm39) |
|
probably null |
Het |
Zscan12 |
C |
A |
13: 21,550,813 (GRCm39) |
T144K |
probably benign |
Het |
|
Other mutations in Son |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00531:Son
|
APN |
16 |
91,461,210 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01024:Son
|
APN |
16 |
91,452,798 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01066:Son
|
APN |
16 |
91,457,024 (GRCm39) |
intron |
probably benign |
|
IGL01083:Son
|
APN |
16 |
91,454,279 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01115:Son
|
APN |
16 |
91,456,346 (GRCm39) |
missense |
probably benign |
0.31 |
IGL01467:Son
|
APN |
16 |
91,454,165 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01506:Son
|
APN |
16 |
91,454,174 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL01933:Son
|
APN |
16 |
91,454,903 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02156:Son
|
APN |
16 |
91,452,992 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02473:Son
|
APN |
16 |
91,455,683 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02498:Son
|
APN |
16 |
91,453,713 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02517:Son
|
APN |
16 |
91,452,099 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02530:Son
|
APN |
16 |
91,455,359 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL02865:Son
|
APN |
16 |
91,448,640 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03180:Son
|
APN |
16 |
91,453,896 (GRCm39) |
missense |
probably damaging |
1.00 |
R0013:Son
|
UTSW |
16 |
91,448,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R0036:Son
|
UTSW |
16 |
91,457,054 (GRCm39) |
intron |
probably benign |
|
R0037:Son
|
UTSW |
16 |
91,461,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R0041:Son
|
UTSW |
16 |
91,456,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R0048:Son
|
UTSW |
16 |
91,455,865 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0048:Son
|
UTSW |
16 |
91,455,865 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0056:Son
|
UTSW |
16 |
91,475,043 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0227:Son
|
UTSW |
16 |
91,453,761 (GRCm39) |
missense |
probably damaging |
0.99 |
R0256:Son
|
UTSW |
16 |
91,453,472 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0302:Son
|
UTSW |
16 |
91,453,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R0815:Son
|
UTSW |
16 |
91,452,372 (GRCm39) |
missense |
probably damaging |
0.98 |
R1225:Son
|
UTSW |
16 |
91,454,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R1255:Son
|
UTSW |
16 |
91,461,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R1457:Son
|
UTSW |
16 |
91,453,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R1459:Son
|
UTSW |
16 |
91,452,230 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1535:Son
|
UTSW |
16 |
91,456,622 (GRCm39) |
missense |
probably damaging |
0.99 |
R1587:Son
|
UTSW |
16 |
91,456,606 (GRCm39) |
missense |
probably damaging |
1.00 |
R1629:Son
|
UTSW |
16 |
91,454,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R1711:Son
|
UTSW |
16 |
91,457,114 (GRCm39) |
intron |
probably benign |
|
R2138:Son
|
UTSW |
16 |
91,456,260 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2245:Son
|
UTSW |
16 |
91,444,848 (GRCm39) |
splice site |
probably null |
|
R2351:Son
|
UTSW |
16 |
91,454,547 (GRCm39) |
missense |
probably damaging |
0.98 |
R2434:Son
|
UTSW |
16 |
91,451,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R2870:Son
|
UTSW |
16 |
91,461,205 (GRCm39) |
splice site |
probably null |
|
R2871:Son
|
UTSW |
16 |
91,461,205 (GRCm39) |
splice site |
probably null |
|
R2872:Son
|
UTSW |
16 |
91,461,205 (GRCm39) |
splice site |
probably null |
|
R2889:Son
|
UTSW |
16 |
91,456,787 (GRCm39) |
unclassified |
probably benign |
|
R3712:Son
|
UTSW |
16 |
91,453,614 (GRCm39) |
missense |
probably damaging |
0.99 |
R3913:Son
|
UTSW |
16 |
91,456,999 (GRCm39) |
intron |
probably benign |
|
R4172:Son
|
UTSW |
16 |
91,456,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R4301:Son
|
UTSW |
16 |
91,455,299 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4302:Son
|
UTSW |
16 |
91,455,299 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4770:Son
|
UTSW |
16 |
91,455,756 (GRCm39) |
missense |
probably damaging |
0.96 |
R4881:Son
|
UTSW |
16 |
91,472,397 (GRCm39) |
missense |
probably benign |
0.31 |
R5020:Son
|
UTSW |
16 |
91,453,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R5032:Son
|
UTSW |
16 |
91,454,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R5151:Son
|
UTSW |
16 |
91,452,587 (GRCm39) |
missense |
probably damaging |
1.00 |
R5153:Son
|
UTSW |
16 |
91,451,910 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5215:Son
|
UTSW |
16 |
91,453,563 (GRCm39) |
missense |
probably damaging |
0.99 |
R5243:Son
|
UTSW |
16 |
91,451,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R5354:Son
|
UTSW |
16 |
91,452,627 (GRCm39) |
missense |
probably damaging |
0.99 |
R5529:Son
|
UTSW |
16 |
91,452,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R5696:Son
|
UTSW |
16 |
91,468,301 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5763:Son
|
UTSW |
16 |
91,454,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R5766:Son
|
UTSW |
16 |
91,461,875 (GRCm39) |
intron |
probably benign |
|
R5788:Son
|
UTSW |
16 |
91,456,940 (GRCm39) |
intron |
probably benign |
|
R5992:Son
|
UTSW |
16 |
91,455,792 (GRCm39) |
missense |
probably benign |
0.04 |
R6314:Son
|
UTSW |
16 |
91,457,298 (GRCm39) |
intron |
probably benign |
|
R6371:Son
|
UTSW |
16 |
91,471,629 (GRCm39) |
|
|
|
R6429:Son
|
UTSW |
16 |
91,455,054 (GRCm39) |
missense |
probably benign |
0.33 |
R6451:Son
|
UTSW |
16 |
91,454,490 (GRCm39) |
missense |
probably damaging |
0.99 |
R6489:Son
|
UTSW |
16 |
91,452,044 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6513:Son
|
UTSW |
16 |
91,456,835 (GRCm39) |
intron |
probably benign |
|
R6753:Son
|
UTSW |
16 |
91,454,076 (GRCm39) |
missense |
probably damaging |
0.99 |
R6916:Son
|
UTSW |
16 |
91,451,673 (GRCm39) |
missense |
probably damaging |
0.97 |
R7070:Son
|
UTSW |
16 |
91,453,729 (GRCm39) |
unclassified |
probably benign |
|
R7079:Son
|
UTSW |
16 |
91,453,729 (GRCm39) |
unclassified |
probably benign |
|
R7110:Son
|
UTSW |
16 |
91,453,406 (GRCm39) |
missense |
probably benign |
0.01 |
R7120:Son
|
UTSW |
16 |
91,467,414 (GRCm39) |
missense |
unknown |
|
R7120:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R7167:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R7205:Son
|
UTSW |
16 |
91,457,183 (GRCm39) |
small deletion |
probably benign |
|
R7208:Son
|
UTSW |
16 |
91,458,990 (GRCm39) |
missense |
unknown |
|
R7219:Son
|
UTSW |
16 |
91,461,889 (GRCm39) |
missense |
unknown |
|
R7249:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R7328:Son
|
UTSW |
16 |
91,455,278 (GRCm39) |
missense |
probably benign |
0.33 |
R7330:Son
|
UTSW |
16 |
91,453,486 (GRCm39) |
unclassified |
probably benign |
|
R7374:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R7405:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R7420:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R7424:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R7464:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R7514:Son
|
UTSW |
16 |
91,451,748 (GRCm39) |
missense |
probably damaging |
0.99 |
R7555:Son
|
UTSW |
16 |
91,455,810 (GRCm39) |
missense |
probably damaging |
0.99 |
R7645:Son
|
UTSW |
16 |
91,457,183 (GRCm39) |
small deletion |
probably benign |
|
R7716:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R7718:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R7778:Son
|
UTSW |
16 |
91,453,416 (GRCm39) |
missense |
probably damaging |
0.99 |
R7824:Son
|
UTSW |
16 |
91,453,416 (GRCm39) |
missense |
probably damaging |
0.99 |
R7856:Son
|
UTSW |
16 |
91,456,146 (GRCm39) |
missense |
probably damaging |
0.99 |
R7870:Son
|
UTSW |
16 |
91,453,486 (GRCm39) |
unclassified |
probably benign |
|
R7928:Son
|
UTSW |
16 |
91,453,729 (GRCm39) |
unclassified |
probably benign |
|
R7972:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R7978:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R8000:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R8192:Son
|
UTSW |
16 |
91,452,437 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8221:Son
|
UTSW |
16 |
91,453,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R8227:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R8233:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R8255:Son
|
UTSW |
16 |
91,461,824 (GRCm39) |
missense |
unknown |
|
R8292:Son
|
UTSW |
16 |
91,453,545 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8407:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R8468:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R8495:Son
|
UTSW |
16 |
91,457,183 (GRCm39) |
small deletion |
probably benign |
|
R8772:Son
|
UTSW |
16 |
91,454,826 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8796:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R8862:Son
|
UTSW |
16 |
91,453,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R8962:Son
|
UTSW |
16 |
91,455,057 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8972:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R8991:Son
|
UTSW |
16 |
91,453,608 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8991:Son
|
UTSW |
16 |
91,453,366 (GRCm39) |
missense |
probably benign |
0.04 |
R9086:Son
|
UTSW |
16 |
91,467,418 (GRCm39) |
missense |
unknown |
|
R9138:Son
|
UTSW |
16 |
91,452,006 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9232:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R9241:Son
|
UTSW |
16 |
91,454,122 (GRCm39) |
missense |
probably damaging |
0.96 |
R9258:Son
|
UTSW |
16 |
91,474,570 (GRCm39) |
missense |
unknown |
|
R9328:Son
|
UTSW |
16 |
91,452,645 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9420:Son
|
UTSW |
16 |
91,454,508 (GRCm39) |
missense |
probably damaging |
0.98 |
R9468:Son
|
UTSW |
16 |
91,454,439 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9500:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R9516:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R9595:Son
|
UTSW |
16 |
91,454,241 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9679:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R9719:Son
|
UTSW |
16 |
91,456,440 (GRCm39) |
missense |
probably damaging |
0.96 |
R9749:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R9772:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R9782:Son
|
UTSW |
16 |
91,444,838 (GRCm39) |
missense |
probably damaging |
0.99 |
R9788:Son
|
UTSW |
16 |
91,453,699 (GRCm39) |
unclassified |
probably benign |
|
RF007:Son
|
UTSW |
16 |
91,456,257 (GRCm39) |
missense |
possibly damaging |
0.53 |
RF041:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
Z1176:Son
|
UTSW |
16 |
91,452,689 (GRCm39) |
missense |
possibly damaging |
0.80 |
|