Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aaas |
A |
C |
15: 102,255,520 (GRCm39) |
D86E |
probably benign |
Het |
Akap3 |
A |
G |
6: 126,843,130 (GRCm39) |
D583G |
possibly damaging |
Het |
Alms1 |
T |
A |
6: 85,598,556 (GRCm39) |
D1127E |
probably benign |
Het |
Anks4b |
T |
A |
7: 119,773,307 (GRCm39) |
|
probably null |
Het |
Ano8 |
A |
T |
8: 71,935,724 (GRCm39) |
F298Y |
probably benign |
Het |
Arhgef2 |
C |
A |
3: 88,536,850 (GRCm39) |
Q7K |
probably benign |
Het |
Brd10 |
T |
C |
19: 29,693,890 (GRCm39) |
I1868V |
probably benign |
Het |
Cand2 |
T |
C |
6: 115,769,941 (GRCm39) |
L917P |
probably damaging |
Het |
Car8 |
T |
C |
4: 8,238,083 (GRCm39) |
D44G |
probably benign |
Het |
Cdk1 |
T |
C |
10: 69,176,435 (GRCm39) |
N224S |
probably benign |
Het |
Cep162 |
T |
C |
9: 87,114,064 (GRCm39) |
E336G |
probably benign |
Het |
Chd7 |
T |
C |
4: 8,866,069 (GRCm39) |
M2792T |
probably benign |
Het |
Cyp4f40 |
A |
T |
17: 32,886,957 (GRCm39) |
K143* |
probably null |
Het |
Cyth1 |
T |
A |
11: 118,074,768 (GRCm39) |
M178L |
probably benign |
Het |
Dcaf11 |
C |
T |
14: 55,798,023 (GRCm39) |
|
probably benign |
Het |
Dlec1 |
T |
G |
9: 118,967,225 (GRCm39) |
W1203G |
probably damaging |
Het |
Fgd4 |
A |
T |
16: 16,302,133 (GRCm39) |
S141T |
probably benign |
Het |
Firrm |
A |
G |
1: 163,786,895 (GRCm39) |
S725P |
probably damaging |
Het |
Flg2 |
T |
A |
3: 93,108,120 (GRCm39) |
D49E |
probably damaging |
Het |
Fyb2 |
T |
A |
4: 104,861,086 (GRCm39) |
D647E |
unknown |
Het |
Gstp1 |
T |
C |
19: 4,086,698 (GRCm39) |
Y109C |
probably damaging |
Het |
Gtf3c3 |
T |
C |
1: 54,468,031 (GRCm39) |
E202G |
probably benign |
Het |
Hephl1 |
A |
G |
9: 14,985,563 (GRCm39) |
F698L |
probably benign |
Het |
Hephl1 |
G |
T |
9: 15,023,280 (GRCm39) |
P41T |
probably damaging |
Het |
Hmcn1 |
T |
A |
1: 150,509,371 (GRCm39) |
E3659V |
probably benign |
Het |
Il27ra |
A |
T |
8: 84,765,988 (GRCm39) |
D229E |
probably damaging |
Het |
Itih2 |
T |
A |
2: 10,103,369 (GRCm39) |
D706V |
probably damaging |
Het |
Itpr2 |
A |
T |
6: 146,133,926 (GRCm39) |
C1893S |
probably benign |
Het |
Lama5 |
T |
C |
2: 179,832,714 (GRCm39) |
N1646S |
probably benign |
Het |
Laptm4b |
A |
G |
15: 34,273,420 (GRCm39) |
D111G |
probably damaging |
Het |
Ldb3 |
T |
A |
14: 34,299,256 (GRCm39) |
S123C |
probably damaging |
Het |
Lgals12 |
C |
T |
19: 7,581,345 (GRCm39) |
E121K |
possibly damaging |
Het |
Mmp13 |
T |
A |
9: 7,277,996 (GRCm39) |
S296R |
possibly damaging |
Het |
Mpeg1 |
T |
C |
19: 12,439,238 (GRCm39) |
F232S |
probably damaging |
Het |
Ncapd2 |
A |
T |
6: 125,148,817 (GRCm39) |
C990S |
possibly damaging |
Het |
Nckap5 |
A |
T |
1: 125,954,279 (GRCm39) |
C758S |
possibly damaging |
Het |
Nwd1 |
A |
T |
8: 73,394,192 (GRCm39) |
D485V |
probably damaging |
Het |
Or13a21 |
T |
G |
7: 139,999,417 (GRCm39) |
S90R |
probably benign |
Het |
Or6c2 |
T |
C |
10: 129,362,332 (GRCm39) |
F79L |
possibly damaging |
Het |
Or8g50 |
T |
A |
9: 39,648,786 (GRCm39) |
I225N |
probably damaging |
Het |
Pcgf3 |
G |
A |
5: 108,634,108 (GRCm39) |
R122Q |
probably benign |
Het |
Pgm5 |
T |
A |
19: 24,812,212 (GRCm39) |
I107F |
probably damaging |
Het |
Pid1 |
G |
T |
1: 84,016,066 (GRCm39) |
H114N |
probably damaging |
Het |
Pkdrej |
T |
C |
15: 85,703,807 (GRCm39) |
T710A |
probably benign |
Het |
Plpbp |
T |
A |
8: 27,535,165 (GRCm39) |
|
probably null |
Het |
Ppfibp2 |
T |
G |
7: 107,343,432 (GRCm39) |
F824V |
probably damaging |
Het |
Ppp1r16b |
G |
A |
2: 158,593,098 (GRCm39) |
D226N |
probably damaging |
Het |
Psg17 |
T |
A |
7: 18,550,836 (GRCm39) |
T340S |
possibly damaging |
Het |
Pstpip2 |
T |
C |
18: 77,961,133 (GRCm39) |
S239P |
probably damaging |
Het |
Ralbp1 |
A |
C |
17: 66,166,036 (GRCm39) |
S383A |
possibly damaging |
Het |
Ranbp2 |
T |
A |
10: 58,300,969 (GRCm39) |
L613* |
probably null |
Het |
Rgs11 |
T |
C |
17: 26,422,346 (GRCm39) |
V49A |
probably damaging |
Het |
Ryr1 |
C |
T |
7: 28,791,693 (GRCm39) |
V1404I |
probably benign |
Het |
Secisbp2 |
G |
A |
13: 51,833,869 (GRCm39) |
V670I |
possibly damaging |
Het |
Slc22a13 |
T |
A |
9: 119,038,126 (GRCm39) |
M1L |
probably damaging |
Het |
Slc5a1 |
A |
T |
5: 33,316,526 (GRCm39) |
I591L |
probably benign |
Het |
Tacr2 |
T |
A |
10: 62,088,733 (GRCm39) |
V46E |
possibly damaging |
Het |
Tet2 |
C |
T |
3: 133,194,039 (GRCm39) |
G132S |
probably damaging |
Het |
Tmco3 |
A |
T |
8: 13,341,782 (GRCm39) |
I19L |
probably benign |
Het |
Tnfrsf1a |
T |
A |
6: 125,334,768 (GRCm39) |
L14Q |
probably benign |
Het |
Tpm1 |
A |
T |
9: 66,935,371 (GRCm39) |
L248Q |
probably benign |
Het |
Tprn |
T |
A |
2: 25,154,027 (GRCm39) |
I443N |
probably benign |
Het |
Unc80 |
A |
T |
1: 66,651,290 (GRCm39) |
H1545L |
possibly damaging |
Het |
Vmn2r97 |
T |
A |
17: 19,168,104 (GRCm39) |
M786K |
probably damaging |
Het |
Wipi1 |
C |
T |
11: 109,494,645 (GRCm39) |
V63M |
probably damaging |
Het |
Zcchc4 |
G |
A |
5: 52,976,724 (GRCm39) |
R506H |
unknown |
Het |
Zfand6 |
A |
T |
7: 84,281,899 (GRCm39) |
V110E |
probably benign |
Het |
Zfp866 |
A |
T |
8: 70,219,381 (GRCm39) |
Y80N |
possibly damaging |
Het |
|
Other mutations in Thsd7a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00562:Thsd7a
|
APN |
6 |
12,379,658 (GRCm39) |
splice site |
probably null |
|
IGL00563:Thsd7a
|
APN |
6 |
12,379,658 (GRCm39) |
splice site |
probably null |
|
IGL00753:Thsd7a
|
APN |
6 |
12,327,528 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00835:Thsd7a
|
APN |
6 |
12,554,933 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01486:Thsd7a
|
APN |
6 |
12,471,079 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01730:Thsd7a
|
APN |
6 |
12,554,980 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01931:Thsd7a
|
APN |
6 |
12,504,098 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01935:Thsd7a
|
APN |
6 |
12,317,418 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01978:Thsd7a
|
APN |
6 |
12,331,005 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02233:Thsd7a
|
APN |
6 |
12,555,257 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02354:Thsd7a
|
APN |
6 |
12,348,192 (GRCm39) |
splice site |
probably benign |
|
IGL02361:Thsd7a
|
APN |
6 |
12,348,192 (GRCm39) |
splice site |
probably benign |
|
IGL02375:Thsd7a
|
APN |
6 |
12,343,264 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02468:Thsd7a
|
APN |
6 |
12,318,170 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02616:Thsd7a
|
APN |
6 |
12,408,984 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02820:Thsd7a
|
APN |
6 |
12,321,071 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02858:Thsd7a
|
APN |
6 |
12,500,994 (GRCm39) |
missense |
probably benign |
0.16 |
IGL03074:Thsd7a
|
APN |
6 |
12,324,680 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03234:Thsd7a
|
APN |
6 |
12,343,177 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03244:Thsd7a
|
APN |
6 |
12,504,167 (GRCm39) |
splice site |
probably benign |
|
IGL03337:Thsd7a
|
APN |
6 |
12,405,173 (GRCm39) |
missense |
probably damaging |
1.00 |
G1patch:Thsd7a
|
UTSW |
6 |
12,555,630 (GRCm39) |
missense |
possibly damaging |
0.87 |
PIT4354001:Thsd7a
|
UTSW |
6 |
12,331,926 (GRCm39) |
critical splice donor site |
probably null |
|
R0095:Thsd7a
|
UTSW |
6 |
12,320,969 (GRCm39) |
missense |
probably damaging |
0.99 |
R0127:Thsd7a
|
UTSW |
6 |
12,554,907 (GRCm39) |
missense |
probably benign |
0.01 |
R0142:Thsd7a
|
UTSW |
6 |
12,418,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R0226:Thsd7a
|
UTSW |
6 |
12,321,899 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0242:Thsd7a
|
UTSW |
6 |
12,503,915 (GRCm39) |
missense |
probably benign |
0.32 |
R0242:Thsd7a
|
UTSW |
6 |
12,503,915 (GRCm39) |
missense |
probably benign |
0.32 |
R0359:Thsd7a
|
UTSW |
6 |
12,352,030 (GRCm39) |
missense |
probably damaging |
1.00 |
R0365:Thsd7a
|
UTSW |
6 |
12,321,886 (GRCm39) |
critical splice donor site |
probably null |
|
R0504:Thsd7a
|
UTSW |
6 |
12,379,593 (GRCm39) |
missense |
probably damaging |
0.99 |
R0512:Thsd7a
|
UTSW |
6 |
12,379,604 (GRCm39) |
missense |
possibly damaging |
0.67 |
R0540:Thsd7a
|
UTSW |
6 |
12,331,541 (GRCm39) |
splice site |
probably null |
|
R0577:Thsd7a
|
UTSW |
6 |
12,321,047 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0607:Thsd7a
|
UTSW |
6 |
12,331,541 (GRCm39) |
splice site |
probably null |
|
R0755:Thsd7a
|
UTSW |
6 |
12,555,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R0771:Thsd7a
|
UTSW |
6 |
12,327,576 (GRCm39) |
missense |
probably benign |
0.09 |
R0780:Thsd7a
|
UTSW |
6 |
12,337,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R0870:Thsd7a
|
UTSW |
6 |
12,337,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R0871:Thsd7a
|
UTSW |
6 |
12,337,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R0872:Thsd7a
|
UTSW |
6 |
12,337,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R0873:Thsd7a
|
UTSW |
6 |
12,337,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R1102:Thsd7a
|
UTSW |
6 |
12,555,701 (GRCm39) |
missense |
possibly damaging |
0.58 |
R1144:Thsd7a
|
UTSW |
6 |
12,471,026 (GRCm39) |
splice site |
probably benign |
|
R1265:Thsd7a
|
UTSW |
6 |
12,317,418 (GRCm39) |
missense |
probably damaging |
0.99 |
R1276:Thsd7a
|
UTSW |
6 |
12,418,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R1381:Thsd7a
|
UTSW |
6 |
12,555,438 (GRCm39) |
missense |
probably damaging |
1.00 |
R1473:Thsd7a
|
UTSW |
6 |
12,338,621 (GRCm39) |
missense |
probably benign |
0.08 |
R1519:Thsd7a
|
UTSW |
6 |
12,471,174 (GRCm39) |
missense |
probably benign |
0.01 |
R1633:Thsd7a
|
UTSW |
6 |
12,471,103 (GRCm39) |
nonsense |
probably null |
|
R1659:Thsd7a
|
UTSW |
6 |
12,504,063 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1769:Thsd7a
|
UTSW |
6 |
12,555,714 (GRCm39) |
nonsense |
probably null |
|
R1824:Thsd7a
|
UTSW |
6 |
12,409,041 (GRCm39) |
splice site |
probably null |
|
R1840:Thsd7a
|
UTSW |
6 |
12,330,973 (GRCm39) |
missense |
probably benign |
0.03 |
R1845:Thsd7a
|
UTSW |
6 |
12,321,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R1874:Thsd7a
|
UTSW |
6 |
12,555,434 (GRCm39) |
missense |
possibly damaging |
0.76 |
R2023:Thsd7a
|
UTSW |
6 |
12,327,535 (GRCm39) |
missense |
probably benign |
0.16 |
R2039:Thsd7a
|
UTSW |
6 |
12,408,922 (GRCm39) |
missense |
possibly damaging |
0.77 |
R2058:Thsd7a
|
UTSW |
6 |
12,318,105 (GRCm39) |
splice site |
probably benign |
|
R2138:Thsd7a
|
UTSW |
6 |
12,471,072 (GRCm39) |
nonsense |
probably null |
|
R2155:Thsd7a
|
UTSW |
6 |
12,379,632 (GRCm39) |
missense |
probably damaging |
1.00 |
R2175:Thsd7a
|
UTSW |
6 |
12,331,943 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2216:Thsd7a
|
UTSW |
6 |
12,337,267 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2318:Thsd7a
|
UTSW |
6 |
12,405,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R2375:Thsd7a
|
UTSW |
6 |
12,337,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R3857:Thsd7a
|
UTSW |
6 |
12,555,225 (GRCm39) |
missense |
probably benign |
0.15 |
R3858:Thsd7a
|
UTSW |
6 |
12,555,225 (GRCm39) |
missense |
probably benign |
0.15 |
R3890:Thsd7a
|
UTSW |
6 |
12,418,336 (GRCm39) |
missense |
probably benign |
0.09 |
R3910:Thsd7a
|
UTSW |
6 |
12,331,548 (GRCm39) |
missense |
probably damaging |
0.96 |
R3933:Thsd7a
|
UTSW |
6 |
12,555,225 (GRCm39) |
missense |
probably benign |
0.15 |
R4369:Thsd7a
|
UTSW |
6 |
12,468,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R4447:Thsd7a
|
UTSW |
6 |
12,324,634 (GRCm39) |
missense |
probably damaging |
0.98 |
R4664:Thsd7a
|
UTSW |
6 |
12,504,012 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4664:Thsd7a
|
UTSW |
6 |
12,337,313 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4665:Thsd7a
|
UTSW |
6 |
12,504,012 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4665:Thsd7a
|
UTSW |
6 |
12,337,313 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4666:Thsd7a
|
UTSW |
6 |
12,504,012 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4666:Thsd7a
|
UTSW |
6 |
12,337,313 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4668:Thsd7a
|
UTSW |
6 |
12,408,967 (GRCm39) |
missense |
probably damaging |
0.98 |
R4886:Thsd7a
|
UTSW |
6 |
12,327,659 (GRCm39) |
nonsense |
probably null |
|
R4918:Thsd7a
|
UTSW |
6 |
12,327,558 (GRCm39) |
missense |
probably damaging |
1.00 |
R4938:Thsd7a
|
UTSW |
6 |
12,330,991 (GRCm39) |
missense |
probably benign |
0.09 |
R5064:Thsd7a
|
UTSW |
6 |
12,330,951 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5153:Thsd7a
|
UTSW |
6 |
12,338,654 (GRCm39) |
missense |
probably benign |
0.00 |
R5177:Thsd7a
|
UTSW |
6 |
12,379,582 (GRCm39) |
nonsense |
probably null |
|
R5242:Thsd7a
|
UTSW |
6 |
12,327,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R5267:Thsd7a
|
UTSW |
6 |
12,379,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R5442:Thsd7a
|
UTSW |
6 |
12,748,799 (GRCm39) |
missense |
probably benign |
0.00 |
R5506:Thsd7a
|
UTSW |
6 |
12,332,016 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5525:Thsd7a
|
UTSW |
6 |
12,332,006 (GRCm39) |
missense |
possibly damaging |
0.52 |
R5544:Thsd7a
|
UTSW |
6 |
12,379,470 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5651:Thsd7a
|
UTSW |
6 |
12,343,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R5716:Thsd7a
|
UTSW |
6 |
12,343,147 (GRCm39) |
missense |
probably benign |
0.00 |
R5848:Thsd7a
|
UTSW |
6 |
12,503,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R5958:Thsd7a
|
UTSW |
6 |
12,337,261 (GRCm39) |
missense |
probably benign |
0.02 |
R6012:Thsd7a
|
UTSW |
6 |
12,379,388 (GRCm39) |
splice site |
probably null |
|
R6139:Thsd7a
|
UTSW |
6 |
12,379,572 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6243:Thsd7a
|
UTSW |
6 |
12,327,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R6257:Thsd7a
|
UTSW |
6 |
12,408,987 (GRCm39) |
nonsense |
probably null |
|
R6273:Thsd7a
|
UTSW |
6 |
12,408,835 (GRCm39) |
missense |
probably damaging |
0.99 |
R6300:Thsd7a
|
UTSW |
6 |
12,471,103 (GRCm39) |
nonsense |
probably null |
|
R6314:Thsd7a
|
UTSW |
6 |
12,554,996 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6392:Thsd7a
|
UTSW |
6 |
12,468,928 (GRCm39) |
missense |
probably damaging |
0.99 |
R6418:Thsd7a
|
UTSW |
6 |
12,555,081 (GRCm39) |
nonsense |
probably null |
|
R6515:Thsd7a
|
UTSW |
6 |
12,501,085 (GRCm39) |
missense |
possibly damaging |
0.47 |
R6725:Thsd7a
|
UTSW |
6 |
12,555,630 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6742:Thsd7a
|
UTSW |
6 |
12,408,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R6776:Thsd7a
|
UTSW |
6 |
12,555,636 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6838:Thsd7a
|
UTSW |
6 |
12,504,074 (GRCm39) |
missense |
probably damaging |
0.99 |
R7104:Thsd7a
|
UTSW |
6 |
12,379,429 (GRCm39) |
missense |
|
|
R7170:Thsd7a
|
UTSW |
6 |
12,352,090 (GRCm39) |
missense |
|
|
R7349:Thsd7a
|
UTSW |
6 |
12,352,067 (GRCm39) |
missense |
|
|
R7460:Thsd7a
|
UTSW |
6 |
12,554,933 (GRCm39) |
missense |
|
|
R7467:Thsd7a
|
UTSW |
6 |
12,331,584 (GRCm39) |
missense |
|
|
R7666:Thsd7a
|
UTSW |
6 |
12,379,437 (GRCm39) |
missense |
|
|
R7869:Thsd7a
|
UTSW |
6 |
12,471,123 (GRCm39) |
nonsense |
probably null |
|
R8032:Thsd7a
|
UTSW |
6 |
12,555,287 (GRCm39) |
missense |
|
|
R8165:Thsd7a
|
UTSW |
6 |
12,468,962 (GRCm39) |
missense |
|
|
R8167:Thsd7a
|
UTSW |
6 |
12,317,400 (GRCm39) |
nonsense |
probably null |
|
R8245:Thsd7a
|
UTSW |
6 |
12,379,592 (GRCm39) |
missense |
|
|
R8310:Thsd7a
|
UTSW |
6 |
12,396,612 (GRCm39) |
missense |
|
|
R8312:Thsd7a
|
UTSW |
6 |
12,471,181 (GRCm39) |
missense |
|
|
R8331:Thsd7a
|
UTSW |
6 |
12,471,157 (GRCm39) |
missense |
|
|
R8843:Thsd7a
|
UTSW |
6 |
12,501,136 (GRCm39) |
missense |
|
|
R8867:Thsd7a
|
UTSW |
6 |
12,338,686 (GRCm39) |
missense |
|
|
R8952:Thsd7a
|
UTSW |
6 |
12,468,992 (GRCm39) |
missense |
probably damaging |
0.98 |
R9036:Thsd7a
|
UTSW |
6 |
12,418,249 (GRCm39) |
missense |
|
|
R9299:Thsd7a
|
UTSW |
6 |
12,504,131 (GRCm39) |
missense |
|
|
R9366:Thsd7a
|
UTSW |
6 |
12,555,480 (GRCm39) |
missense |
|
|
R9489:Thsd7a
|
UTSW |
6 |
12,352,022 (GRCm39) |
missense |
|
|
|