Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
8430408G22Rik |
A |
T |
6: 116,652,262 (GRCm38) |
S189C |
possibly damaging |
Het |
Acp1 |
C |
T |
12: 30,895,935 (GRCm38) |
E140K |
possibly damaging |
Het |
Acsm4 |
T |
A |
7: 119,693,819 (GRCm38) |
D57E |
probably damaging |
Het |
Adamts9 |
A |
G |
6: 92,849,290 (GRCm38) |
|
probably null |
Het |
Aen |
T |
A |
7: 78,907,312 (GRCm38) |
Y303N |
probably damaging |
Het |
Alcam |
T |
C |
16: 52,295,752 (GRCm38) |
|
probably null |
Het |
Apol7b |
A |
G |
15: 77,425,546 (GRCm38) |
L17P |
probably damaging |
Het |
Cacna1c |
A |
T |
6: 118,652,793 (GRCm38) |
Y1058* |
probably null |
Het |
Camk2d |
T |
C |
3: 126,808,224 (GRCm38) |
V354A |
probably benign |
Het |
Carf |
T |
G |
1: 60,124,858 (GRCm38) |
M43R |
probably damaging |
Het |
Casp8 |
T |
A |
1: 58,824,124 (GRCm38) |
F81Y |
probably damaging |
Het |
Cd74 |
G |
A |
18: 60,803,992 (GRCm38) |
R20H |
probably benign |
Het |
Cers5 |
A |
T |
15: 99,745,931 (GRCm38) |
Y16* |
probably null |
Het |
Chuk |
A |
T |
19: 44,078,958 (GRCm38) |
M586K |
probably null |
Het |
D130043K22Rik |
C |
A |
13: 24,871,341 (GRCm38) |
P496Q |
probably damaging |
Het |
Dab2 |
A |
G |
15: 6,429,938 (GRCm38) |
R311G |
probably damaging |
Het |
Diaph1 |
A |
T |
18: 37,905,134 (GRCm38) |
I48N |
unknown |
Het |
Dnajc13 |
T |
C |
9: 104,180,121 (GRCm38) |
D1560G |
probably damaging |
Het |
Dsg2 |
T |
C |
18: 20,582,723 (GRCm38) |
S241P |
probably damaging |
Het |
Efcab5 |
T |
C |
11: 77,105,378 (GRCm38) |
D1119G |
probably benign |
Het |
Efr3a |
G |
T |
15: 65,869,057 (GRCm38) |
|
probably benign |
Het |
Evc2 |
A |
G |
5: 37,393,083 (GRCm38) |
K814E |
probably damaging |
Het |
Gm5724 |
A |
G |
6: 141,765,703 (GRCm38) |
M94T |
probably benign |
Het |
Hic2 |
A |
G |
16: 17,258,822 (GRCm38) |
D505G |
probably benign |
Het |
Ing1 |
T |
A |
8: 11,557,010 (GRCm38) |
V34D |
probably damaging |
Het |
Inpp5k |
A |
G |
11: 75,637,491 (GRCm38) |
M172V |
probably benign |
Het |
Itgae |
T |
C |
11: 73,115,592 (GRCm38) |
V362A |
probably damaging |
Het |
Lama2 |
T |
A |
10: 27,187,754 (GRCm38) |
R1346S |
probably damaging |
Het |
Lrrc7 |
T |
C |
3: 158,177,306 (GRCm38) |
N450S |
probably damaging |
Het |
Lrrn3 |
T |
A |
12: 41,452,584 (GRCm38) |
Y578F |
possibly damaging |
Het |
Maml2 |
A |
T |
9: 13,706,501 (GRCm38) |
N381I |
probably damaging |
Het |
Mettl15 |
T |
G |
2: 109,092,921 (GRCm38) |
E385D |
probably benign |
Het |
Mthfr |
T |
A |
4: 148,055,443 (GRCm38) |
I623N |
possibly damaging |
Het |
Muc4 |
A |
C |
16: 32,753,020 (GRCm38) |
N966T |
probably benign |
Het |
Myoc |
A |
G |
1: 162,648,996 (GRCm38) |
Y423C |
probably damaging |
Het |
Ncoa2 |
A |
T |
1: 13,148,378 (GRCm38) |
M1409K |
probably benign |
Het |
Ncor2 |
T |
C |
5: 125,109,975 (GRCm38) |
|
probably benign |
Het |
Numb |
T |
C |
12: 83,797,259 (GRCm38) |
E395G |
probably damaging |
Het |
Oas1g |
A |
G |
5: 120,881,949 (GRCm38) |
F198S |
probably damaging |
Het |
Olfr1367 |
T |
C |
13: 21,347,024 (GRCm38) |
V32A |
probably benign |
Het |
Olfr181 |
A |
G |
16: 58,925,686 (GRCm38) |
V295A |
probably benign |
Het |
Prdm13 |
T |
A |
4: 21,678,909 (GRCm38) |
Y527F |
probably damaging |
Het |
Prr14l |
A |
G |
5: 32,828,833 (GRCm38) |
L1106P |
probably damaging |
Het |
Ptbp1 |
T |
A |
10: 79,863,273 (GRCm38) |
I555N |
probably damaging |
Het |
Ptchd4 |
A |
T |
17: 42,503,715 (GRCm38) |
T836S |
possibly damaging |
Het |
Rlbp1 |
T |
C |
7: 79,383,938 (GRCm38) |
D3G |
probably benign |
Het |
Serpinc1 |
A |
T |
1: 160,993,404 (GRCm38) |
K140N |
probably damaging |
Het |
Serpind1 |
A |
T |
16: 17,342,385 (GRCm38) |
Y382F |
probably damaging |
Het |
Slc28a3 |
T |
C |
13: 58,563,106 (GRCm38) |
E534G |
probably damaging |
Het |
Ttyh2 |
T |
A |
11: 114,710,179 (GRCm38) |
I418N |
probably benign |
Het |
Tubgcp4 |
C |
T |
2: 121,175,424 (GRCm38) |
Q98* |
probably null |
Het |
Ugt2a2 |
A |
G |
5: 87,464,106 (GRCm38) |
L315P |
probably damaging |
Het |
Vwa1 |
A |
T |
4: 155,772,901 (GRCm38) |
S147T |
probably damaging |
Het |
Xylt1 |
T |
C |
7: 117,591,952 (GRCm38) |
V325A |
possibly damaging |
Het |
Zfp335 |
T |
C |
2: 164,899,456 (GRCm38) |
H685R |
probably damaging |
Het |
|
Other mutations in Sdk2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00972:Sdk2
|
APN |
11 |
113,854,384 (GRCm38) |
missense |
possibly damaging |
0.86 |
IGL01063:Sdk2
|
APN |
11 |
113,830,842 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01291:Sdk2
|
APN |
11 |
113,843,080 (GRCm38) |
missense |
probably benign |
|
IGL01316:Sdk2
|
APN |
11 |
113,867,965 (GRCm38) |
missense |
probably benign |
0.09 |
IGL01614:Sdk2
|
APN |
11 |
113,793,858 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01998:Sdk2
|
APN |
11 |
113,838,532 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL02014:Sdk2
|
APN |
11 |
113,838,494 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02095:Sdk2
|
APN |
11 |
113,834,830 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02115:Sdk2
|
APN |
11 |
113,834,813 (GRCm38) |
splice site |
probably benign |
|
IGL02543:Sdk2
|
APN |
11 |
113,868,921 (GRCm38) |
missense |
possibly damaging |
0.90 |
IGL02976:Sdk2
|
APN |
11 |
113,851,842 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03001:Sdk2
|
APN |
11 |
113,821,626 (GRCm38) |
missense |
probably benign |
0.00 |
IGL03122:Sdk2
|
APN |
11 |
113,842,068 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03183:Sdk2
|
APN |
11 |
113,850,984 (GRCm38) |
missense |
probably benign |
0.19 |
IGL03222:Sdk2
|
APN |
11 |
113,838,431 (GRCm38) |
missense |
probably benign |
0.01 |
IGL03310:Sdk2
|
APN |
11 |
113,793,325 (GRCm38) |
missense |
possibly damaging |
0.77 |
Curtailed
|
UTSW |
11 |
113,851,800 (GRCm38) |
missense |
probably damaging |
1.00 |
Trimmed
|
UTSW |
11 |
113,856,696 (GRCm38) |
nonsense |
probably null |
|
ANU05:Sdk2
|
UTSW |
11 |
113,843,080 (GRCm38) |
missense |
probably benign |
|
BB008:Sdk2
|
UTSW |
11 |
113,893,441 (GRCm38) |
missense |
possibly damaging |
0.79 |
BB018:Sdk2
|
UTSW |
11 |
113,893,441 (GRCm38) |
missense |
possibly damaging |
0.79 |
R0008:Sdk2
|
UTSW |
11 |
113,856,755 (GRCm38) |
missense |
probably damaging |
1.00 |
R0008:Sdk2
|
UTSW |
11 |
113,856,755 (GRCm38) |
missense |
probably damaging |
1.00 |
R0088:Sdk2
|
UTSW |
11 |
113,827,086 (GRCm38) |
missense |
possibly damaging |
0.74 |
R0096:Sdk2
|
UTSW |
11 |
113,903,144 (GRCm38) |
splice site |
probably benign |
|
R0386:Sdk2
|
UTSW |
11 |
113,893,464 (GRCm38) |
missense |
probably damaging |
0.96 |
R0396:Sdk2
|
UTSW |
11 |
113,829,967 (GRCm38) |
missense |
probably benign |
0.04 |
R0409:Sdk2
|
UTSW |
11 |
113,850,891 (GRCm38) |
splice site |
probably benign |
|
R0416:Sdk2
|
UTSW |
11 |
113,803,203 (GRCm38) |
missense |
probably damaging |
1.00 |
R0456:Sdk2
|
UTSW |
11 |
113,791,466 (GRCm38) |
missense |
possibly damaging |
0.93 |
R0544:Sdk2
|
UTSW |
11 |
113,781,010 (GRCm38) |
missense |
probably damaging |
1.00 |
R0691:Sdk2
|
UTSW |
11 |
113,794,920 (GRCm38) |
splice site |
probably null |
|
R0711:Sdk2
|
UTSW |
11 |
113,903,144 (GRCm38) |
splice site |
probably benign |
|
R0717:Sdk2
|
UTSW |
11 |
113,832,326 (GRCm38) |
missense |
probably damaging |
1.00 |
R0780:Sdk2
|
UTSW |
11 |
113,893,508 (GRCm38) |
missense |
probably benign |
0.07 |
R0831:Sdk2
|
UTSW |
11 |
113,832,258 (GRCm38) |
missense |
probably damaging |
0.96 |
R0853:Sdk2
|
UTSW |
11 |
113,821,415 (GRCm38) |
missense |
probably benign |
0.00 |
R0865:Sdk2
|
UTSW |
11 |
113,850,922 (GRCm38) |
missense |
probably benign |
0.12 |
R0930:Sdk2
|
UTSW |
11 |
113,838,445 (GRCm38) |
missense |
probably benign |
0.01 |
R0964:Sdk2
|
UTSW |
11 |
113,806,417 (GRCm38) |
splice site |
probably benign |
|
R1051:Sdk2
|
UTSW |
11 |
113,838,646 (GRCm38) |
synonymous |
silent |
|
R1052:Sdk2
|
UTSW |
11 |
113,838,646 (GRCm38) |
synonymous |
silent |
|
R1054:Sdk2
|
UTSW |
11 |
113,838,646 (GRCm38) |
synonymous |
silent |
|
R1055:Sdk2
|
UTSW |
11 |
113,838,646 (GRCm38) |
synonymous |
silent |
|
R1077:Sdk2
|
UTSW |
11 |
113,838,646 (GRCm38) |
synonymous |
silent |
|
R1079:Sdk2
|
UTSW |
11 |
113,838,646 (GRCm38) |
synonymous |
silent |
|
R1115:Sdk2
|
UTSW |
11 |
113,838,646 (GRCm38) |
synonymous |
silent |
|
R1186:Sdk2
|
UTSW |
11 |
113,838,646 (GRCm38) |
synonymous |
silent |
|
R1187:Sdk2
|
UTSW |
11 |
113,838,646 (GRCm38) |
synonymous |
silent |
|
R1337:Sdk2
|
UTSW |
11 |
113,832,331 (GRCm38) |
missense |
possibly damaging |
0.79 |
R1430:Sdk2
|
UTSW |
11 |
113,838,646 (GRCm38) |
synonymous |
silent |
|
R1464:Sdk2
|
UTSW |
11 |
113,830,080 (GRCm38) |
missense |
possibly damaging |
0.86 |
R1464:Sdk2
|
UTSW |
11 |
113,830,080 (GRCm38) |
missense |
possibly damaging |
0.86 |
R1497:Sdk2
|
UTSW |
11 |
113,893,575 (GRCm38) |
splice site |
probably benign |
|
R1514:Sdk2
|
UTSW |
11 |
113,838,646 (GRCm38) |
synonymous |
silent |
|
R1529:Sdk2
|
UTSW |
11 |
113,838,646 (GRCm38) |
synonymous |
silent |
|
R1596:Sdk2
|
UTSW |
11 |
113,838,609 (GRCm38) |
splice site |
probably benign |
|
R1680:Sdk2
|
UTSW |
11 |
113,838,646 (GRCm38) |
synonymous |
silent |
|
R1680:Sdk2
|
UTSW |
11 |
113,791,436 (GRCm38) |
missense |
possibly damaging |
0.47 |
R1770:Sdk2
|
UTSW |
11 |
113,793,741 (GRCm38) |
missense |
probably benign |
0.05 |
R1858:Sdk2
|
UTSW |
11 |
113,838,646 (GRCm38) |
synonymous |
silent |
|
R1866:Sdk2
|
UTSW |
11 |
113,838,646 (GRCm38) |
synonymous |
silent |
|
R1874:Sdk2
|
UTSW |
11 |
113,834,956 (GRCm38) |
missense |
probably benign |
0.00 |
R1899:Sdk2
|
UTSW |
11 |
113,838,646 (GRCm38) |
synonymous |
silent |
|
R1905:Sdk2
|
UTSW |
11 |
113,838,646 (GRCm38) |
synonymous |
silent |
|
R1907:Sdk2
|
UTSW |
11 |
113,838,646 (GRCm38) |
synonymous |
silent |
|
R1913:Sdk2
|
UTSW |
11 |
113,856,726 (GRCm38) |
missense |
possibly damaging |
0.77 |
R1964:Sdk2
|
UTSW |
11 |
113,781,017 (GRCm38) |
nonsense |
probably null |
|
R2055:Sdk2
|
UTSW |
11 |
113,850,954 (GRCm38) |
missense |
probably damaging |
1.00 |
R2059:Sdk2
|
UTSW |
11 |
113,854,332 (GRCm38) |
missense |
probably damaging |
1.00 |
R2093:Sdk2
|
UTSW |
11 |
113,943,122 (GRCm38) |
missense |
probably damaging |
1.00 |
R2256:Sdk2
|
UTSW |
11 |
113,830,794 (GRCm38) |
missense |
probably benign |
0.44 |
R3720:Sdk2
|
UTSW |
11 |
113,800,244 (GRCm38) |
missense |
probably damaging |
1.00 |
R3795:Sdk2
|
UTSW |
11 |
113,856,696 (GRCm38) |
nonsense |
probably null |
|
R4037:Sdk2
|
UTSW |
11 |
113,795,055 (GRCm38) |
missense |
probably damaging |
1.00 |
R4171:Sdk2
|
UTSW |
11 |
113,866,989 (GRCm38) |
splice site |
probably null |
|
R4717:Sdk2
|
UTSW |
11 |
113,854,369 (GRCm38) |
missense |
probably damaging |
0.96 |
R4758:Sdk2
|
UTSW |
11 |
113,827,054 (GRCm38) |
missense |
possibly damaging |
0.87 |
R4857:Sdk2
|
UTSW |
11 |
113,821,382 (GRCm38) |
nonsense |
probably null |
|
R4924:Sdk2
|
UTSW |
11 |
113,857,758 (GRCm38) |
missense |
probably damaging |
1.00 |
R5015:Sdk2
|
UTSW |
11 |
113,793,761 (GRCm38) |
missense |
probably damaging |
1.00 |
R5171:Sdk2
|
UTSW |
11 |
113,850,982 (GRCm38) |
missense |
probably benign |
0.01 |
R5239:Sdk2
|
UTSW |
11 |
113,868,033 (GRCm38) |
missense |
probably damaging |
1.00 |
R5243:Sdk2
|
UTSW |
11 |
113,825,086 (GRCm38) |
missense |
possibly damaging |
0.76 |
R5279:Sdk2
|
UTSW |
11 |
113,867,031 (GRCm38) |
missense |
probably benign |
0.31 |
R5535:Sdk2
|
UTSW |
11 |
113,943,158 (GRCm38) |
missense |
possibly damaging |
0.80 |
R5634:Sdk2
|
UTSW |
11 |
113,851,714 (GRCm38) |
missense |
probably damaging |
1.00 |
R5637:Sdk2
|
UTSW |
11 |
113,833,179 (GRCm38) |
missense |
probably damaging |
1.00 |
R5726:Sdk2
|
UTSW |
11 |
113,851,800 (GRCm38) |
missense |
probably damaging |
1.00 |
R5793:Sdk2
|
UTSW |
11 |
113,868,952 (GRCm38) |
missense |
possibly damaging |
0.46 |
R5798:Sdk2
|
UTSW |
11 |
113,827,116 (GRCm38) |
missense |
probably damaging |
1.00 |
R5834:Sdk2
|
UTSW |
11 |
113,854,273 (GRCm38) |
missense |
probably damaging |
1.00 |
R5863:Sdk2
|
UTSW |
11 |
113,834,984 (GRCm38) |
missense |
probably damaging |
0.98 |
R5869:Sdk2
|
UTSW |
11 |
113,851,882 (GRCm38) |
missense |
probably damaging |
0.96 |
R5875:Sdk2
|
UTSW |
11 |
113,830,059 (GRCm38) |
missense |
probably benign |
0.00 |
R5953:Sdk2
|
UTSW |
11 |
113,793,744 (GRCm38) |
missense |
probably damaging |
1.00 |
R5991:Sdk2
|
UTSW |
11 |
113,943,254 (GRCm38) |
missense |
probably damaging |
0.97 |
R6018:Sdk2
|
UTSW |
11 |
113,830,063 (GRCm38) |
missense |
probably benign |
0.00 |
R6116:Sdk2
|
UTSW |
11 |
113,854,364 (GRCm38) |
missense |
probably damaging |
0.99 |
R6328:Sdk2
|
UTSW |
11 |
113,793,755 (GRCm38) |
missense |
probably damaging |
1.00 |
R6348:Sdk2
|
UTSW |
11 |
113,893,508 (GRCm38) |
missense |
probably benign |
0.07 |
R6383:Sdk2
|
UTSW |
11 |
113,832,265 (GRCm38) |
missense |
probably damaging |
1.00 |
R6824:Sdk2
|
UTSW |
11 |
113,867,934 (GRCm38) |
missense |
probably benign |
0.43 |
R6835:Sdk2
|
UTSW |
11 |
113,830,048 (GRCm38) |
missense |
probably damaging |
0.98 |
R6853:Sdk2
|
UTSW |
11 |
113,780,929 (GRCm38) |
missense |
probably damaging |
0.99 |
R6912:Sdk2
|
UTSW |
11 |
113,903,120 (GRCm38) |
missense |
probably benign |
0.03 |
R7000:Sdk2
|
UTSW |
11 |
113,803,169 (GRCm38) |
missense |
probably damaging |
1.00 |
R7099:Sdk2
|
UTSW |
11 |
113,834,905 (GRCm38) |
missense |
probably damaging |
0.98 |
R7102:Sdk2
|
UTSW |
11 |
113,842,690 (GRCm38) |
nonsense |
probably null |
|
R7177:Sdk2
|
UTSW |
11 |
113,829,969 (GRCm38) |
missense |
possibly damaging |
0.91 |
R7381:Sdk2
|
UTSW |
11 |
113,838,489 (GRCm38) |
missense |
probably damaging |
0.98 |
R7412:Sdk2
|
UTSW |
11 |
113,868,083 (GRCm38) |
splice site |
probably null |
|
R7504:Sdk2
|
UTSW |
11 |
113,867,967 (GRCm38) |
missense |
possibly damaging |
0.50 |
R7552:Sdk2
|
UTSW |
11 |
113,873,213 (GRCm38) |
missense |
possibly damaging |
0.63 |
R7604:Sdk2
|
UTSW |
11 |
113,829,969 (GRCm38) |
missense |
possibly damaging |
0.91 |
R7647:Sdk2
|
UTSW |
11 |
113,793,737 (GRCm38) |
missense |
probably damaging |
1.00 |
R7897:Sdk2
|
UTSW |
11 |
113,873,201 (GRCm38) |
missense |
possibly damaging |
0.50 |
R7931:Sdk2
|
UTSW |
11 |
113,893,441 (GRCm38) |
missense |
possibly damaging |
0.79 |
R7998:Sdk2
|
UTSW |
11 |
113,859,938 (GRCm38) |
missense |
probably benign |
0.18 |
R8052:Sdk2
|
UTSW |
11 |
113,854,351 (GRCm38) |
missense |
probably damaging |
1.00 |
R8053:Sdk2
|
UTSW |
11 |
113,854,351 (GRCm38) |
missense |
probably damaging |
1.00 |
R8084:Sdk2
|
UTSW |
11 |
113,827,089 (GRCm38) |
missense |
possibly damaging |
0.67 |
R8136:Sdk2
|
UTSW |
11 |
113,851,713 (GRCm38) |
missense |
probably damaging |
1.00 |
R8151:Sdk2
|
UTSW |
11 |
113,872,857 (GRCm38) |
missense |
possibly damaging |
0.84 |
R8394:Sdk2
|
UTSW |
11 |
113,838,716 (GRCm38) |
missense |
probably benign |
|
R8715:Sdk2
|
UTSW |
11 |
113,780,902 (GRCm38) |
missense |
probably damaging |
1.00 |
R8774:Sdk2
|
UTSW |
11 |
113,839,343 (GRCm38) |
missense |
probably damaging |
1.00 |
R8774-TAIL:Sdk2
|
UTSW |
11 |
113,839,343 (GRCm38) |
missense |
probably damaging |
1.00 |
R8804:Sdk2
|
UTSW |
11 |
113,873,152 (GRCm38) |
nonsense |
probably null |
|
R9136:Sdk2
|
UTSW |
11 |
113,806,377 (GRCm38) |
missense |
probably damaging |
1.00 |
R9147:Sdk2
|
UTSW |
11 |
113,823,400 (GRCm38) |
missense |
probably benign |
0.18 |
R9300:Sdk2
|
UTSW |
11 |
113,825,030 (GRCm38) |
missense |
possibly damaging |
0.63 |
R9354:Sdk2
|
UTSW |
11 |
113,834,931 (GRCm38) |
missense |
probably benign |
0.00 |
R9450:Sdk2
|
UTSW |
11 |
113,806,279 (GRCm38) |
missense |
probably benign |
|
R9462:Sdk2
|
UTSW |
11 |
113,869,918 (GRCm38) |
missense |
possibly damaging |
0.56 |
R9616:Sdk2
|
UTSW |
11 |
113,800,235 (GRCm38) |
missense |
probably benign |
0.05 |
R9678:Sdk2
|
UTSW |
11 |
113,794,963 (GRCm38) |
nonsense |
probably null |
|
RF002:Sdk2
|
UTSW |
11 |
113,885,252 (GRCm38) |
missense |
probably benign |
0.00 |
V1662:Sdk2
|
UTSW |
11 |
113,834,908 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1176:Sdk2
|
UTSW |
11 |
113,851,836 (GRCm38) |
missense |
probably damaging |
0.97 |
Z1176:Sdk2
|
UTSW |
11 |
113,839,322 (GRCm38) |
missense |
probably benign |
0.41 |
Z1177:Sdk2
|
UTSW |
11 |
113,859,956 (GRCm38) |
missense |
probably benign |
|
Z1177:Sdk2
|
UTSW |
11 |
113,839,320 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1177:Sdk2
|
UTSW |
11 |
113,838,659 (GRCm38) |
missense |
probably damaging |
0.99 |
|