Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aamdc |
T |
A |
7: 97,214,432 (GRCm39) |
T48S |
probably benign |
Het |
Abcc3 |
T |
A |
11: 94,247,802 (GRCm39) |
L1230F |
probably damaging |
Het |
Abcf3 |
T |
A |
16: 20,378,114 (GRCm39) |
I542N |
probably benign |
Het |
Als2 |
A |
G |
1: 59,226,508 (GRCm39) |
L932P |
probably damaging |
Het |
Arhgap45 |
G |
A |
10: 79,862,281 (GRCm39) |
R583H |
probably damaging |
Het |
Asl |
T |
C |
5: 130,042,245 (GRCm39) |
Y277C |
probably damaging |
Het |
Bcl9 |
A |
T |
3: 97,112,989 (GRCm39) |
N1155K |
possibly damaging |
Het |
Carm1 |
C |
A |
9: 21,490,692 (GRCm39) |
|
probably null |
Het |
Cdkn2aip |
T |
C |
8: 48,164,532 (GRCm39) |
K394E |
probably damaging |
Het |
Cfap70 |
A |
G |
14: 20,470,830 (GRCm39) |
Y472H |
probably damaging |
Het |
Cfap77 |
T |
A |
2: 28,852,662 (GRCm39) |
K203N |
probably damaging |
Het |
Cldn14 |
T |
C |
16: 93,716,192 (GRCm39) |
K218R |
probably damaging |
Het |
Coro6 |
T |
C |
11: 77,359,738 (GRCm39) |
F336S |
probably damaging |
Het |
Derl1 |
C |
A |
15: 57,739,007 (GRCm39) |
|
probably benign |
Het |
Dixdc1 |
G |
A |
9: 50,622,259 (GRCm39) |
A25V |
probably damaging |
Het |
Dock2 |
T |
A |
11: 34,181,610 (GRCm39) |
H1651L |
probably benign |
Het |
Dock6 |
A |
G |
9: 21,750,496 (GRCm39) |
F473L |
possibly damaging |
Het |
Dzip3 |
T |
C |
16: 48,747,921 (GRCm39) |
H1163R |
probably damaging |
Het |
Efcab9 |
T |
C |
11: 32,473,689 (GRCm39) |
D35G |
probably benign |
Het |
Evpl |
T |
C |
11: 116,111,678 (GRCm39) |
D2004G |
probably damaging |
Het |
Faiml |
A |
G |
9: 99,114,527 (GRCm39) |
C121R |
probably damaging |
Het |
Fastkd3 |
T |
C |
13: 68,732,987 (GRCm39) |
V436A |
probably benign |
Het |
Fbxl5 |
A |
G |
5: 43,908,222 (GRCm39) |
Y660H |
probably damaging |
Het |
Glt8d1 |
T |
C |
14: 30,728,617 (GRCm39) |
V15A |
probably benign |
Het |
Gpr25 |
A |
C |
1: 136,187,623 (GRCm39) |
I330S |
possibly damaging |
Het |
Hdac5 |
A |
T |
11: 102,096,436 (GRCm39) |
V257E |
probably damaging |
Het |
Lama2 |
C |
T |
10: 26,877,231 (GRCm39) |
E2652K |
probably benign |
Het |
Lrriq1 |
T |
A |
10: 102,980,750 (GRCm39) |
S1462C |
probably damaging |
Het |
Mgat3 |
A |
G |
15: 80,096,055 (GRCm39) |
D294G |
probably benign |
Het |
Mylk2 |
A |
G |
2: 152,761,274 (GRCm39) |
N459S |
probably benign |
Het |
Myo3b |
A |
C |
2: 70,086,927 (GRCm39) |
|
probably benign |
Het |
Nfxl1 |
C |
T |
5: 72,686,378 (GRCm39) |
A608T |
possibly damaging |
Het |
Nmd3 |
A |
G |
3: 69,631,732 (GRCm39) |
|
probably benign |
Het |
Nol8 |
C |
T |
13: 49,831,868 (GRCm39) |
|
probably benign |
Het |
Or1e29 |
A |
T |
11: 73,668,051 (GRCm39) |
M34K |
probably damaging |
Het |
Or8b12i |
C |
A |
9: 20,082,061 (GRCm39) |
G269W |
probably benign |
Het |
Or8b42 |
T |
A |
9: 38,342,352 (GRCm39) |
M258K |
possibly damaging |
Het |
Or8g34 |
G |
A |
9: 39,373,226 (GRCm39) |
M166I |
probably benign |
Het |
Pcdhgb2 |
T |
C |
18: 37,824,566 (GRCm39) |
F519S |
probably damaging |
Het |
Phf11c |
A |
G |
14: 59,618,933 (GRCm39) |
V284A |
probably benign |
Het |
Rasl11a |
G |
T |
5: 146,784,113 (GRCm39) |
C186F |
probably benign |
Het |
Rps18-ps3 |
T |
C |
8: 107,989,469 (GRCm39) |
|
noncoding transcript |
Het |
Rusc1 |
A |
G |
3: 88,999,030 (GRCm39) |
S251P |
possibly damaging |
Het |
Rxfp3 |
T |
C |
15: 11,037,303 (GRCm39) |
E23G |
probably benign |
Het |
Senp6 |
G |
A |
9: 80,051,124 (GRCm39) |
A1134T |
probably benign |
Het |
Slc22a4 |
A |
G |
11: 53,898,615 (GRCm39) |
V159A |
probably benign |
Het |
Spata31d1a |
T |
C |
13: 59,850,907 (GRCm39) |
N407S |
probably benign |
Het |
Ssc4d |
T |
C |
5: 135,994,578 (GRCm39) |
T51A |
possibly damaging |
Het |
Stip1 |
C |
T |
19: 7,013,016 (GRCm39) |
A23T |
probably benign |
Het |
Tecta |
A |
T |
9: 42,289,290 (GRCm39) |
M425K |
possibly damaging |
Het |
Tmed4 |
T |
C |
11: 6,224,151 (GRCm39) |
H115R |
probably benign |
Het |
Tmem255b |
T |
A |
8: 13,501,048 (GRCm39) |
L74H |
probably damaging |
Het |
Trav6n-5 |
A |
T |
14: 53,342,741 (GRCm39) |
H93L |
possibly damaging |
Het |
Tsen54 |
T |
A |
11: 115,710,990 (GRCm39) |
D187E |
probably benign |
Het |
Ttc39d |
A |
G |
17: 80,524,982 (GRCm39) |
Y547C |
probably damaging |
Het |
Vmn2r88 |
A |
G |
14: 51,656,089 (GRCm39) |
N775S |
probably damaging |
Het |
Vps13a |
G |
T |
19: 16,642,101 (GRCm39) |
N2175K |
probably benign |
Het |
Wnk4 |
A |
G |
11: 101,167,717 (GRCm39) |
|
probably benign |
Het |
Zfp180 |
A |
T |
7: 23,804,928 (GRCm39) |
Q449L |
probably damaging |
Het |
|
Other mutations in Naip6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00677:Naip6
|
APN |
13 |
100,452,525 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01123:Naip6
|
APN |
13 |
100,440,946 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01151:Naip6
|
APN |
13 |
100,435,601 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01382:Naip6
|
APN |
13 |
100,436,364 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01415:Naip6
|
APN |
13 |
100,439,798 (GRCm39) |
missense |
probably benign |
0.17 |
IGL01654:Naip6
|
APN |
13 |
100,435,853 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01662:Naip6
|
APN |
13 |
100,436,862 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01726:Naip6
|
APN |
13 |
100,439,760 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01810:Naip6
|
APN |
13 |
100,424,603 (GRCm39) |
splice site |
probably benign |
|
IGL01867:Naip6
|
APN |
13 |
100,436,820 (GRCm39) |
missense |
probably benign |
0.40 |
IGL01926:Naip6
|
APN |
13 |
100,436,704 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01964:Naip6
|
APN |
13 |
100,435,238 (GRCm39) |
splice site |
probably benign |
|
IGL02145:Naip6
|
APN |
13 |
100,433,486 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL02160:Naip6
|
APN |
13 |
100,435,933 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02214:Naip6
|
APN |
13 |
100,452,567 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02342:Naip6
|
APN |
13 |
100,439,748 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL02568:Naip6
|
APN |
13 |
100,452,780 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02573:Naip6
|
APN |
13 |
100,435,979 (GRCm39) |
nonsense |
probably null |
|
IGL02680:Naip6
|
APN |
13 |
100,420,256 (GRCm39) |
missense |
probably benign |
|
IGL02829:Naip6
|
APN |
13 |
100,437,273 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02833:Naip6
|
APN |
13 |
100,436,121 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02851:Naip6
|
APN |
13 |
100,437,168 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02860:Naip6
|
APN |
13 |
100,436,984 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02886:Naip6
|
APN |
13 |
100,436,984 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03155:Naip6
|
APN |
13 |
100,452,932 (GRCm39) |
missense |
possibly damaging |
0.62 |
R0032:Naip6
|
UTSW |
13 |
100,439,745 (GRCm39) |
missense |
probably benign |
0.00 |
R0310:Naip6
|
UTSW |
13 |
100,444,721 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0437:Naip6
|
UTSW |
13 |
100,433,432 (GRCm39) |
missense |
possibly damaging |
0.75 |
R0472:Naip6
|
UTSW |
13 |
100,438,768 (GRCm39) |
missense |
probably benign |
0.02 |
R0560:Naip6
|
UTSW |
13 |
100,437,108 (GRCm39) |
missense |
probably benign |
0.08 |
R0638:Naip6
|
UTSW |
13 |
100,437,036 (GRCm39) |
missense |
probably benign |
0.00 |
R0792:Naip6
|
UTSW |
13 |
100,420,274 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0963:Naip6
|
UTSW |
13 |
100,452,983 (GRCm39) |
missense |
probably benign |
0.11 |
R1102:Naip6
|
UTSW |
13 |
100,440,923 (GRCm39) |
missense |
possibly damaging |
0.62 |
R1278:Naip6
|
UTSW |
13 |
100,436,870 (GRCm39) |
missense |
probably damaging |
1.00 |
R1462:Naip6
|
UTSW |
13 |
100,436,748 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1462:Naip6
|
UTSW |
13 |
100,436,748 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1544:Naip6
|
UTSW |
13 |
100,452,983 (GRCm39) |
missense |
probably benign |
|
R1595:Naip6
|
UTSW |
13 |
100,435,602 (GRCm39) |
missense |
probably damaging |
0.96 |
R1749:Naip6
|
UTSW |
13 |
100,444,763 (GRCm39) |
missense |
probably benign |
0.03 |
R1838:Naip6
|
UTSW |
13 |
100,452,644 (GRCm39) |
missense |
probably damaging |
0.99 |
R1863:Naip6
|
UTSW |
13 |
100,437,067 (GRCm39) |
missense |
probably benign |
0.03 |
R1914:Naip6
|
UTSW |
13 |
100,435,936 (GRCm39) |
missense |
probably benign |
0.13 |
R2001:Naip6
|
UTSW |
13 |
100,437,237 (GRCm39) |
missense |
probably benign |
0.44 |
R2082:Naip6
|
UTSW |
13 |
100,440,852 (GRCm39) |
splice site |
probably null |
|
R2143:Naip6
|
UTSW |
13 |
100,436,367 (GRCm39) |
missense |
probably damaging |
1.00 |
R2174:Naip6
|
UTSW |
13 |
100,435,495 (GRCm39) |
missense |
probably benign |
|
R2266:Naip6
|
UTSW |
13 |
100,420,067 (GRCm39) |
missense |
possibly damaging |
0.46 |
R2284:Naip6
|
UTSW |
13 |
100,437,108 (GRCm39) |
missense |
probably benign |
0.08 |
R2285:Naip6
|
UTSW |
13 |
100,437,108 (GRCm39) |
missense |
probably benign |
0.08 |
R2286:Naip6
|
UTSW |
13 |
100,437,108 (GRCm39) |
missense |
probably benign |
0.08 |
R2351:Naip6
|
UTSW |
13 |
100,420,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R2363:Naip6
|
UTSW |
13 |
100,452,928 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2445:Naip6
|
UTSW |
13 |
100,437,176 (GRCm39) |
missense |
probably damaging |
0.99 |
R2971:Naip6
|
UTSW |
13 |
100,437,108 (GRCm39) |
missense |
probably benign |
0.08 |
R2975:Naip6
|
UTSW |
13 |
100,424,695 (GRCm39) |
missense |
probably damaging |
1.00 |
R3082:Naip6
|
UTSW |
13 |
100,452,925 (GRCm39) |
missense |
probably benign |
0.00 |
R3122:Naip6
|
UTSW |
13 |
100,453,031 (GRCm39) |
missense |
probably benign |
0.00 |
R3417:Naip6
|
UTSW |
13 |
100,437,108 (GRCm39) |
missense |
probably benign |
0.08 |
R3943:Naip6
|
UTSW |
13 |
100,431,247 (GRCm39) |
missense |
probably benign |
0.01 |
R3944:Naip6
|
UTSW |
13 |
100,431,247 (GRCm39) |
missense |
probably benign |
0.01 |
R4080:Naip6
|
UTSW |
13 |
100,435,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R4166:Naip6
|
UTSW |
13 |
100,452,657 (GRCm39) |
missense |
probably benign |
0.23 |
R4396:Naip6
|
UTSW |
13 |
100,437,108 (GRCm39) |
missense |
probably benign |
0.08 |
R4397:Naip6
|
UTSW |
13 |
100,437,108 (GRCm39) |
missense |
probably benign |
0.08 |
R4418:Naip6
|
UTSW |
13 |
100,437,108 (GRCm39) |
missense |
probably benign |
0.08 |
R4512:Naip6
|
UTSW |
13 |
100,437,108 (GRCm39) |
missense |
probably benign |
0.08 |
R4670:Naip6
|
UTSW |
13 |
100,431,239 (GRCm39) |
critical splice donor site |
probably null |
|
R4671:Naip6
|
UTSW |
13 |
100,431,239 (GRCm39) |
critical splice donor site |
probably null |
|
R4722:Naip6
|
UTSW |
13 |
100,443,580 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4811:Naip6
|
UTSW |
13 |
100,422,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R4900:Naip6
|
UTSW |
13 |
100,433,477 (GRCm39) |
missense |
probably damaging |
0.99 |
R5162:Naip6
|
UTSW |
13 |
100,437,108 (GRCm39) |
missense |
probably benign |
0.08 |
R5316:Naip6
|
UTSW |
13 |
100,420,290 (GRCm39) |
missense |
probably benign |
0.00 |
R5403:Naip6
|
UTSW |
13 |
100,436,585 (GRCm39) |
missense |
probably benign |
0.12 |
R5437:Naip6
|
UTSW |
13 |
100,439,812 (GRCm39) |
nonsense |
probably null |
|
R5507:Naip6
|
UTSW |
13 |
100,435,423 (GRCm39) |
missense |
probably benign |
0.01 |
R5631:Naip6
|
UTSW |
13 |
100,436,646 (GRCm39) |
missense |
probably benign |
0.02 |
R5657:Naip6
|
UTSW |
13 |
100,436,909 (GRCm39) |
missense |
probably benign |
|
R5684:Naip6
|
UTSW |
13 |
100,436,888 (GRCm39) |
missense |
probably damaging |
1.00 |
R5786:Naip6
|
UTSW |
13 |
100,436,724 (GRCm39) |
missense |
probably benign |
|
R5787:Naip6
|
UTSW |
13 |
100,436,724 (GRCm39) |
missense |
probably benign |
|
R5788:Naip6
|
UTSW |
13 |
100,436,724 (GRCm39) |
missense |
probably benign |
|
R5878:Naip6
|
UTSW |
13 |
100,436,181 (GRCm39) |
missense |
probably damaging |
1.00 |
R5895:Naip6
|
UTSW |
13 |
100,452,500 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5898:Naip6
|
UTSW |
13 |
100,435,829 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6113:Naip6
|
UTSW |
13 |
100,435,794 (GRCm39) |
missense |
possibly damaging |
0.96 |
R6141:Naip6
|
UTSW |
13 |
100,444,741 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6199:Naip6
|
UTSW |
13 |
100,437,108 (GRCm39) |
missense |
probably benign |
0.08 |
R6321:Naip6
|
UTSW |
13 |
100,436,909 (GRCm39) |
missense |
probably benign |
|
R6402:Naip6
|
UTSW |
13 |
100,437,226 (GRCm39) |
missense |
probably benign |
0.30 |
R6435:Naip6
|
UTSW |
13 |
100,431,249 (GRCm39) |
missense |
probably benign |
0.04 |
R6477:Naip6
|
UTSW |
13 |
100,452,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R6601:Naip6
|
UTSW |
13 |
100,420,266 (GRCm39) |
missense |
probably benign |
|
R6638:Naip6
|
UTSW |
13 |
100,436,909 (GRCm39) |
missense |
probably benign |
|
R6639:Naip6
|
UTSW |
13 |
100,436,909 (GRCm39) |
missense |
probably benign |
|
R6804:Naip6
|
UTSW |
13 |
100,435,675 (GRCm39) |
missense |
probably benign |
|
R6922:Naip6
|
UTSW |
13 |
100,438,706 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6975:Naip6
|
UTSW |
13 |
100,452,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R7050:Naip6
|
UTSW |
13 |
100,452,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R7135:Naip6
|
UTSW |
13 |
100,436,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R7140:Naip6
|
UTSW |
13 |
100,436,708 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7182:Naip6
|
UTSW |
13 |
100,452,657 (GRCm39) |
missense |
probably benign |
0.23 |
R7196:Naip6
|
UTSW |
13 |
100,436,666 (GRCm39) |
missense |
probably benign |
0.10 |
R7234:Naip6
|
UTSW |
13 |
100,452,011 (GRCm39) |
nonsense |
probably null |
|
R7259:Naip6
|
UTSW |
13 |
100,440,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R7322:Naip6
|
UTSW |
13 |
100,435,896 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7332:Naip6
|
UTSW |
13 |
100,437,209 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7339:Naip6
|
UTSW |
13 |
100,452,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R7353:Naip6
|
UTSW |
13 |
100,436,259 (GRCm39) |
missense |
probably benign |
0.00 |
R7485:Naip6
|
UTSW |
13 |
100,420,359 (GRCm39) |
missense |
probably benign |
0.07 |
R7597:Naip6
|
UTSW |
13 |
100,437,108 (GRCm39) |
missense |
probably benign |
0.08 |
R7835:Naip6
|
UTSW |
13 |
100,452,512 (GRCm39) |
missense |
probably benign |
0.19 |
R7840:Naip6
|
UTSW |
13 |
100,451,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R8082:Naip6
|
UTSW |
13 |
100,436,961 (GRCm39) |
missense |
probably benign |
|
R8082:Naip6
|
UTSW |
13 |
100,436,909 (GRCm39) |
missense |
probably benign |
|
R8103:Naip6
|
UTSW |
13 |
100,437,851 (GRCm39) |
missense |
probably benign |
0.00 |
R8164:Naip6
|
UTSW |
13 |
100,452,797 (GRCm39) |
missense |
probably benign |
0.00 |
R8206:Naip6
|
UTSW |
13 |
100,431,344 (GRCm39) |
nonsense |
probably null |
|
R8258:Naip6
|
UTSW |
13 |
100,452,920 (GRCm39) |
missense |
probably benign |
0.02 |
R8259:Naip6
|
UTSW |
13 |
100,452,920 (GRCm39) |
missense |
probably benign |
0.02 |
R8348:Naip6
|
UTSW |
13 |
100,436,894 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8405:Naip6
|
UTSW |
13 |
100,436,784 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8406:Naip6
|
UTSW |
13 |
100,436,784 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8441:Naip6
|
UTSW |
13 |
100,422,265 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8448:Naip6
|
UTSW |
13 |
100,436,894 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8465:Naip6
|
UTSW |
13 |
100,433,423 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8501:Naip6
|
UTSW |
13 |
100,436,784 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8502:Naip6
|
UTSW |
13 |
100,436,784 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8687:Naip6
|
UTSW |
13 |
100,435,636 (GRCm39) |
missense |
probably benign |
0.10 |
R8806:Naip6
|
UTSW |
13 |
100,437,161 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9186:Naip6
|
UTSW |
13 |
100,436,390 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9340:Naip6
|
UTSW |
13 |
100,452,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R9352:Naip6
|
UTSW |
13 |
100,437,893 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9585:Naip6
|
UTSW |
13 |
100,436,577 (GRCm39) |
missense |
probably damaging |
0.96 |
R9597:Naip6
|
UTSW |
13 |
100,436,646 (GRCm39) |
missense |
probably benign |
0.02 |
R9601:Naip6
|
UTSW |
13 |
100,436,961 (GRCm39) |
missense |
probably benign |
|
X0066:Naip6
|
UTSW |
13 |
100,451,970 (GRCm39) |
nonsense |
probably null |
|
Z1177:Naip6
|
UTSW |
13 |
100,437,308 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Naip6
|
UTSW |
13 |
100,435,925 (GRCm39) |
missense |
probably benign |
0.20 |
Z1177:Naip6
|
UTSW |
13 |
100,452,638 (GRCm39) |
missense |
probably damaging |
1.00 |
|