Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930568D16Rik |
T |
C |
2: 35,244,848 (GRCm39) |
N168S |
probably benign |
Het |
Adam3 |
T |
A |
8: 25,184,207 (GRCm39) |
T598S |
possibly damaging |
Het |
Ago1 |
G |
T |
4: 126,335,008 (GRCm39) |
H405N |
probably damaging |
Het |
Atp8b4 |
T |
C |
2: 126,234,781 (GRCm39) |
|
probably null |
Het |
Baz1a |
A |
G |
12: 54,945,129 (GRCm39) |
S1409P |
probably damaging |
Het |
Brinp2 |
T |
C |
1: 158,078,908 (GRCm39) |
E305G |
probably benign |
Het |
Bub1 |
T |
A |
2: 127,663,616 (GRCm39) |
R262W |
probably damaging |
Het |
Cish |
T |
A |
9: 107,177,111 (GRCm39) |
|
probably null |
Het |
Clip4 |
T |
A |
17: 72,106,072 (GRCm39) |
I85K |
probably damaging |
Het |
Cpsf2 |
T |
A |
12: 101,953,532 (GRCm39) |
C187* |
probably null |
Het |
Ddx51 |
C |
A |
5: 110,801,514 (GRCm39) |
T54K |
probably benign |
Het |
Drc1 |
A |
T |
5: 30,520,467 (GRCm39) |
T603S |
probably benign |
Het |
Eif3l |
T |
A |
15: 78,973,995 (GRCm39) |
M470K |
possibly damaging |
Het |
Entpd2 |
A |
G |
2: 25,290,830 (GRCm39) |
T445A |
probably damaging |
Het |
Epha1 |
C |
A |
6: 42,341,944 (GRCm39) |
V369L |
possibly damaging |
Het |
Galnt9 |
T |
A |
5: 110,692,635 (GRCm39) |
L23H |
probably damaging |
Het |
Gm1110 |
A |
G |
9: 26,804,866 (GRCm39) |
F399S |
probably benign |
Het |
Gm43972 |
G |
A |
5: 25,866,119 (GRCm39) |
|
noncoding transcript |
Het |
Gm6489 |
T |
A |
1: 31,326,351 (GRCm39) |
|
noncoding transcript |
Het |
Grik5 |
A |
T |
7: 24,764,895 (GRCm39) |
M82K |
probably damaging |
Het |
Hibch |
T |
C |
1: 52,904,767 (GRCm39) |
Y121H |
probably damaging |
Het |
Hyou1 |
T |
A |
9: 44,296,560 (GRCm39) |
I495N |
possibly damaging |
Het |
Il1rl2 |
T |
C |
1: 40,404,255 (GRCm39) |
S459P |
probably benign |
Het |
Kel |
A |
T |
6: 41,665,048 (GRCm39) |
L254* |
probably null |
Het |
Lasp1 |
A |
G |
11: 97,690,686 (GRCm39) |
K23E |
probably damaging |
Het |
Lemd2 |
C |
A |
17: 27,422,773 (GRCm39) |
R207L |
possibly damaging |
Het |
Myh1 |
A |
T |
11: 67,106,051 (GRCm39) |
Q1222L |
probably benign |
Het |
Myh2 |
G |
A |
11: 67,083,269 (GRCm39) |
V1411I |
probably benign |
Het |
Myo1f |
T |
C |
17: 33,820,709 (GRCm39) |
F851L |
probably benign |
Het |
Myom3 |
G |
A |
4: 135,528,303 (GRCm39) |
|
probably benign |
Het |
Nbas |
C |
A |
12: 13,491,519 (GRCm39) |
L1464I |
probably benign |
Het |
Nr2e3 |
G |
T |
9: 59,857,059 (GRCm39) |
|
probably benign |
Het |
Nrxn1 |
T |
C |
17: 91,011,537 (GRCm39) |
D364G |
probably damaging |
Het |
Or2y1 |
A |
G |
11: 49,385,555 (GRCm39) |
H65R |
possibly damaging |
Het |
Or5p68 |
T |
A |
7: 107,945,853 (GRCm39) |
T112S |
probably benign |
Het |
Or8g54 |
T |
A |
9: 39,707,492 (GRCm39) |
S274T |
probably damaging |
Het |
Or9g4b |
T |
G |
2: 85,616,002 (GRCm39) |
I49S |
probably damaging |
Het |
Otog |
T |
A |
7: 45,936,859 (GRCm39) |
S1523T |
probably benign |
Het |
Pcnx2 |
A |
T |
8: 126,587,821 (GRCm39) |
|
probably null |
Het |
Pkdcc |
C |
A |
17: 83,523,413 (GRCm39) |
H173Q |
probably damaging |
Het |
Pkn1 |
A |
G |
8: 84,410,811 (GRCm39) |
L267P |
probably damaging |
Het |
Polr1a |
A |
G |
6: 71,890,021 (GRCm39) |
H80R |
probably damaging |
Het |
Pwwp3a |
C |
T |
10: 80,064,255 (GRCm39) |
R14* |
probably null |
Het |
Rag1 |
G |
T |
2: 101,473,300 (GRCm39) |
A614E |
possibly damaging |
Het |
Ryr1 |
T |
C |
7: 28,735,553 (GRCm39) |
D4075G |
probably damaging |
Het |
Smoc2 |
A |
G |
17: 14,589,227 (GRCm39) |
N232S |
probably benign |
Het |
Snd1 |
T |
C |
6: 28,545,524 (GRCm39) |
L360P |
probably damaging |
Het |
Tmem26 |
T |
A |
10: 68,587,096 (GRCm39) |
F181L |
probably damaging |
Het |
Tnrc6a |
A |
G |
7: 122,785,842 (GRCm39) |
M1512V |
probably benign |
Het |
Tsc22d1 |
T |
A |
14: 76,655,852 (GRCm39) |
I20N |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,641,587 (GRCm39) |
L5176Q |
possibly damaging |
Het |
Vmn1r122 |
T |
C |
7: 20,868,023 (GRCm39) |
T11A |
possibly damaging |
Het |
Vpreb1a |
A |
T |
16: 16,686,592 (GRCm39) |
Y99* |
probably null |
Het |
Wnt9b |
A |
T |
11: 103,622,054 (GRCm39) |
|
probably null |
Het |
Zfp143 |
A |
G |
7: 109,693,559 (GRCm39) |
E604G |
probably damaging |
Het |
|
Other mutations in Sdk2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00972:Sdk2
|
APN |
11 |
113,745,210 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL01063:Sdk2
|
APN |
11 |
113,721,668 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01291:Sdk2
|
APN |
11 |
113,733,906 (GRCm39) |
missense |
probably benign |
|
IGL01316:Sdk2
|
APN |
11 |
113,758,791 (GRCm39) |
missense |
probably benign |
0.09 |
IGL01614:Sdk2
|
APN |
11 |
113,684,684 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01998:Sdk2
|
APN |
11 |
113,729,358 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02014:Sdk2
|
APN |
11 |
113,729,320 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02095:Sdk2
|
APN |
11 |
113,725,656 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02115:Sdk2
|
APN |
11 |
113,725,639 (GRCm39) |
splice site |
probably benign |
|
IGL02543:Sdk2
|
APN |
11 |
113,759,747 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02976:Sdk2
|
APN |
11 |
113,742,668 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03001:Sdk2
|
APN |
11 |
113,712,452 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03122:Sdk2
|
APN |
11 |
113,732,894 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03183:Sdk2
|
APN |
11 |
113,741,810 (GRCm39) |
missense |
probably benign |
0.19 |
IGL03222:Sdk2
|
APN |
11 |
113,729,257 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03310:Sdk2
|
APN |
11 |
113,684,151 (GRCm39) |
missense |
possibly damaging |
0.77 |
Curtailed
|
UTSW |
11 |
113,742,626 (GRCm39) |
missense |
probably damaging |
1.00 |
Trimmed
|
UTSW |
11 |
113,747,522 (GRCm39) |
nonsense |
probably null |
|
ANU05:Sdk2
|
UTSW |
11 |
113,733,906 (GRCm39) |
missense |
probably benign |
|
BB008:Sdk2
|
UTSW |
11 |
113,784,267 (GRCm39) |
missense |
possibly damaging |
0.79 |
BB018:Sdk2
|
UTSW |
11 |
113,784,267 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0008:Sdk2
|
UTSW |
11 |
113,747,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R0008:Sdk2
|
UTSW |
11 |
113,747,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R0088:Sdk2
|
UTSW |
11 |
113,717,912 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0096:Sdk2
|
UTSW |
11 |
113,793,970 (GRCm39) |
splice site |
probably benign |
|
R0386:Sdk2
|
UTSW |
11 |
113,784,290 (GRCm39) |
missense |
probably damaging |
0.96 |
R0396:Sdk2
|
UTSW |
11 |
113,720,793 (GRCm39) |
missense |
probably benign |
0.04 |
R0409:Sdk2
|
UTSW |
11 |
113,741,717 (GRCm39) |
splice site |
probably benign |
|
R0416:Sdk2
|
UTSW |
11 |
113,694,029 (GRCm39) |
missense |
probably damaging |
1.00 |
R0456:Sdk2
|
UTSW |
11 |
113,682,292 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0544:Sdk2
|
UTSW |
11 |
113,671,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R0691:Sdk2
|
UTSW |
11 |
113,685,746 (GRCm39) |
splice site |
probably null |
|
R0711:Sdk2
|
UTSW |
11 |
113,793,970 (GRCm39) |
splice site |
probably benign |
|
R0717:Sdk2
|
UTSW |
11 |
113,723,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R0780:Sdk2
|
UTSW |
11 |
113,784,334 (GRCm39) |
missense |
probably benign |
0.07 |
R0831:Sdk2
|
UTSW |
11 |
113,723,084 (GRCm39) |
missense |
probably damaging |
0.96 |
R0853:Sdk2
|
UTSW |
11 |
113,712,241 (GRCm39) |
missense |
probably benign |
0.00 |
R0865:Sdk2
|
UTSW |
11 |
113,741,748 (GRCm39) |
missense |
probably benign |
0.12 |
R0930:Sdk2
|
UTSW |
11 |
113,729,271 (GRCm39) |
missense |
probably benign |
0.01 |
R0964:Sdk2
|
UTSW |
11 |
113,697,243 (GRCm39) |
splice site |
probably benign |
|
R1051:Sdk2
|
UTSW |
11 |
113,729,472 (GRCm39) |
synonymous |
silent |
|
R1052:Sdk2
|
UTSW |
11 |
113,729,472 (GRCm39) |
synonymous |
silent |
|
R1054:Sdk2
|
UTSW |
11 |
113,729,472 (GRCm39) |
synonymous |
silent |
|
R1055:Sdk2
|
UTSW |
11 |
113,729,472 (GRCm39) |
synonymous |
silent |
|
R1077:Sdk2
|
UTSW |
11 |
113,729,472 (GRCm39) |
synonymous |
silent |
|
R1079:Sdk2
|
UTSW |
11 |
113,729,472 (GRCm39) |
synonymous |
silent |
|
R1115:Sdk2
|
UTSW |
11 |
113,729,472 (GRCm39) |
synonymous |
silent |
|
R1186:Sdk2
|
UTSW |
11 |
113,729,472 (GRCm39) |
synonymous |
silent |
|
R1187:Sdk2
|
UTSW |
11 |
113,729,472 (GRCm39) |
synonymous |
silent |
|
R1337:Sdk2
|
UTSW |
11 |
113,723,157 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1430:Sdk2
|
UTSW |
11 |
113,729,472 (GRCm39) |
synonymous |
silent |
|
R1433:Sdk2
|
UTSW |
11 |
113,685,871 (GRCm39) |
missense |
probably damaging |
0.99 |
R1464:Sdk2
|
UTSW |
11 |
113,720,906 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1464:Sdk2
|
UTSW |
11 |
113,720,906 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1497:Sdk2
|
UTSW |
11 |
113,784,401 (GRCm39) |
splice site |
probably benign |
|
R1514:Sdk2
|
UTSW |
11 |
113,729,472 (GRCm39) |
synonymous |
silent |
|
R1529:Sdk2
|
UTSW |
11 |
113,729,472 (GRCm39) |
synonymous |
silent |
|
R1596:Sdk2
|
UTSW |
11 |
113,729,435 (GRCm39) |
splice site |
probably benign |
|
R1680:Sdk2
|
UTSW |
11 |
113,729,472 (GRCm39) |
synonymous |
silent |
|
R1680:Sdk2
|
UTSW |
11 |
113,682,262 (GRCm39) |
missense |
possibly damaging |
0.47 |
R1770:Sdk2
|
UTSW |
11 |
113,684,567 (GRCm39) |
missense |
probably benign |
0.05 |
R1858:Sdk2
|
UTSW |
11 |
113,729,472 (GRCm39) |
synonymous |
silent |
|
R1866:Sdk2
|
UTSW |
11 |
113,729,472 (GRCm39) |
synonymous |
silent |
|
R1874:Sdk2
|
UTSW |
11 |
113,725,782 (GRCm39) |
missense |
probably benign |
0.00 |
R1899:Sdk2
|
UTSW |
11 |
113,729,472 (GRCm39) |
synonymous |
silent |
|
R1905:Sdk2
|
UTSW |
11 |
113,729,472 (GRCm39) |
synonymous |
silent |
|
R1907:Sdk2
|
UTSW |
11 |
113,729,472 (GRCm39) |
synonymous |
silent |
|
R1913:Sdk2
|
UTSW |
11 |
113,747,552 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1964:Sdk2
|
UTSW |
11 |
113,671,843 (GRCm39) |
nonsense |
probably null |
|
R2055:Sdk2
|
UTSW |
11 |
113,741,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R2059:Sdk2
|
UTSW |
11 |
113,745,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R2093:Sdk2
|
UTSW |
11 |
113,833,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R2256:Sdk2
|
UTSW |
11 |
113,721,620 (GRCm39) |
missense |
probably benign |
0.44 |
R3720:Sdk2
|
UTSW |
11 |
113,691,070 (GRCm39) |
missense |
probably damaging |
1.00 |
R3795:Sdk2
|
UTSW |
11 |
113,747,522 (GRCm39) |
nonsense |
probably null |
|
R4037:Sdk2
|
UTSW |
11 |
113,685,881 (GRCm39) |
missense |
probably damaging |
1.00 |
R4171:Sdk2
|
UTSW |
11 |
113,757,815 (GRCm39) |
splice site |
probably null |
|
R4717:Sdk2
|
UTSW |
11 |
113,745,195 (GRCm39) |
missense |
probably damaging |
0.96 |
R4758:Sdk2
|
UTSW |
11 |
113,717,880 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4857:Sdk2
|
UTSW |
11 |
113,712,208 (GRCm39) |
nonsense |
probably null |
|
R4924:Sdk2
|
UTSW |
11 |
113,748,584 (GRCm39) |
missense |
probably damaging |
1.00 |
R5015:Sdk2
|
UTSW |
11 |
113,684,587 (GRCm39) |
missense |
probably damaging |
1.00 |
R5171:Sdk2
|
UTSW |
11 |
113,741,808 (GRCm39) |
missense |
probably benign |
0.01 |
R5243:Sdk2
|
UTSW |
11 |
113,715,912 (GRCm39) |
missense |
possibly damaging |
0.76 |
R5279:Sdk2
|
UTSW |
11 |
113,757,857 (GRCm39) |
missense |
probably benign |
0.31 |
R5535:Sdk2
|
UTSW |
11 |
113,833,984 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5634:Sdk2
|
UTSW |
11 |
113,742,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R5637:Sdk2
|
UTSW |
11 |
113,724,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R5726:Sdk2
|
UTSW |
11 |
113,742,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R5793:Sdk2
|
UTSW |
11 |
113,759,778 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5798:Sdk2
|
UTSW |
11 |
113,717,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R5834:Sdk2
|
UTSW |
11 |
113,745,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R5863:Sdk2
|
UTSW |
11 |
113,725,810 (GRCm39) |
missense |
probably damaging |
0.98 |
R5869:Sdk2
|
UTSW |
11 |
113,742,708 (GRCm39) |
missense |
probably damaging |
0.96 |
R5875:Sdk2
|
UTSW |
11 |
113,720,885 (GRCm39) |
missense |
probably benign |
0.00 |
R5953:Sdk2
|
UTSW |
11 |
113,684,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R5991:Sdk2
|
UTSW |
11 |
113,834,080 (GRCm39) |
missense |
probably damaging |
0.97 |
R6018:Sdk2
|
UTSW |
11 |
113,720,889 (GRCm39) |
missense |
probably benign |
0.00 |
R6116:Sdk2
|
UTSW |
11 |
113,745,190 (GRCm39) |
missense |
probably damaging |
0.99 |
R6328:Sdk2
|
UTSW |
11 |
113,684,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R6348:Sdk2
|
UTSW |
11 |
113,784,334 (GRCm39) |
missense |
probably benign |
0.07 |
R6383:Sdk2
|
UTSW |
11 |
113,723,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R6824:Sdk2
|
UTSW |
11 |
113,758,760 (GRCm39) |
missense |
probably benign |
0.43 |
R6835:Sdk2
|
UTSW |
11 |
113,720,874 (GRCm39) |
missense |
probably damaging |
0.98 |
R6853:Sdk2
|
UTSW |
11 |
113,671,755 (GRCm39) |
missense |
probably damaging |
0.99 |
R6912:Sdk2
|
UTSW |
11 |
113,793,946 (GRCm39) |
missense |
probably benign |
0.03 |
R7000:Sdk2
|
UTSW |
11 |
113,693,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R7099:Sdk2
|
UTSW |
11 |
113,725,731 (GRCm39) |
missense |
probably damaging |
0.98 |
R7102:Sdk2
|
UTSW |
11 |
113,733,516 (GRCm39) |
nonsense |
probably null |
|
R7177:Sdk2
|
UTSW |
11 |
113,720,795 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7381:Sdk2
|
UTSW |
11 |
113,729,315 (GRCm39) |
missense |
probably damaging |
0.98 |
R7412:Sdk2
|
UTSW |
11 |
113,758,909 (GRCm39) |
splice site |
probably null |
|
R7504:Sdk2
|
UTSW |
11 |
113,758,793 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7552:Sdk2
|
UTSW |
11 |
113,764,039 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7604:Sdk2
|
UTSW |
11 |
113,720,795 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7647:Sdk2
|
UTSW |
11 |
113,684,563 (GRCm39) |
missense |
probably damaging |
1.00 |
R7897:Sdk2
|
UTSW |
11 |
113,764,027 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7931:Sdk2
|
UTSW |
11 |
113,784,267 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7998:Sdk2
|
UTSW |
11 |
113,750,764 (GRCm39) |
missense |
probably benign |
0.18 |
R8052:Sdk2
|
UTSW |
11 |
113,745,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R8053:Sdk2
|
UTSW |
11 |
113,745,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R8084:Sdk2
|
UTSW |
11 |
113,717,915 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8136:Sdk2
|
UTSW |
11 |
113,742,539 (GRCm39) |
missense |
probably damaging |
1.00 |
R8151:Sdk2
|
UTSW |
11 |
113,763,683 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8394:Sdk2
|
UTSW |
11 |
113,729,542 (GRCm39) |
missense |
probably benign |
|
R8715:Sdk2
|
UTSW |
11 |
113,671,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R8774:Sdk2
|
UTSW |
11 |
113,730,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R8774-TAIL:Sdk2
|
UTSW |
11 |
113,730,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R8804:Sdk2
|
UTSW |
11 |
113,763,978 (GRCm39) |
nonsense |
probably null |
|
R9136:Sdk2
|
UTSW |
11 |
113,697,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R9147:Sdk2
|
UTSW |
11 |
113,714,226 (GRCm39) |
missense |
probably benign |
0.18 |
R9300:Sdk2
|
UTSW |
11 |
113,715,856 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9354:Sdk2
|
UTSW |
11 |
113,725,757 (GRCm39) |
missense |
probably benign |
0.00 |
R9450:Sdk2
|
UTSW |
11 |
113,697,105 (GRCm39) |
missense |
probably benign |
|
R9462:Sdk2
|
UTSW |
11 |
113,760,744 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9616:Sdk2
|
UTSW |
11 |
113,691,061 (GRCm39) |
missense |
probably benign |
0.05 |
R9678:Sdk2
|
UTSW |
11 |
113,685,789 (GRCm39) |
nonsense |
probably null |
|
RF002:Sdk2
|
UTSW |
11 |
113,776,078 (GRCm39) |
missense |
probably benign |
0.00 |
V1662:Sdk2
|
UTSW |
11 |
113,725,734 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Sdk2
|
UTSW |
11 |
113,742,662 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1176:Sdk2
|
UTSW |
11 |
113,730,148 (GRCm39) |
missense |
probably benign |
0.41 |
Z1177:Sdk2
|
UTSW |
11 |
113,750,782 (GRCm39) |
missense |
probably benign |
|
Z1177:Sdk2
|
UTSW |
11 |
113,730,146 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Sdk2
|
UTSW |
11 |
113,729,485 (GRCm39) |
missense |
probably damaging |
0.99 |
|