Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsf2 |
G |
T |
11: 94,453,700 (GRCm39) |
N420K |
probably benign |
Het |
Adam26a |
A |
T |
8: 44,022,229 (GRCm39) |
C420* |
probably null |
Het |
Afap1l1 |
T |
C |
18: 61,874,909 (GRCm39) |
Y424C |
probably damaging |
Het |
Agl |
A |
G |
3: 116,576,246 (GRCm39) |
V553A |
probably benign |
Het |
Akr7a5 |
T |
A |
4: 139,045,434 (GRCm39) |
M325K |
probably damaging |
Het |
Aldh7a1 |
C |
A |
18: 56,692,341 (GRCm39) |
E87* |
probably null |
Het |
Arhgap29 |
A |
G |
3: 121,767,578 (GRCm39) |
K7E |
probably damaging |
Het |
Brca2 |
T |
A |
5: 150,466,114 (GRCm39) |
D1959E |
probably benign |
Het |
Cdh20 |
G |
A |
1: 109,988,862 (GRCm39) |
V255I |
probably benign |
Het |
Chil5 |
G |
T |
3: 105,925,409 (GRCm39) |
Q171K |
probably benign |
Het |
Cul9 |
C |
G |
17: 46,833,101 (GRCm39) |
A1326P |
probably damaging |
Het |
Dhrs7c |
A |
T |
11: 67,702,476 (GRCm39) |
I155F |
probably damaging |
Het |
Dip2c |
A |
G |
13: 9,603,300 (GRCm39) |
|
probably null |
Het |
Fam124b |
T |
C |
1: 80,191,056 (GRCm39) |
Y109C |
possibly damaging |
Het |
Gak |
T |
A |
5: 108,739,011 (GRCm39) |
K156M |
probably damaging |
Het |
Gm17535 |
A |
G |
9: 3,035,804 (GRCm39) |
Y224C |
probably null |
Het |
Got1l1 |
C |
G |
8: 27,690,745 (GRCm39) |
|
probably null |
Het |
Grm1 |
T |
C |
10: 10,955,879 (GRCm39) |
D135G |
probably benign |
Het |
Hrh3 |
T |
G |
2: 179,744,547 (GRCm39) |
D131A |
probably damaging |
Het |
Itpr1 |
A |
T |
6: 108,366,514 (GRCm39) |
Q979L |
probably null |
Het |
Klb |
G |
C |
5: 65,506,089 (GRCm39) |
R112P |
possibly damaging |
Het |
Lingo2 |
A |
T |
4: 35,709,420 (GRCm39) |
C187S |
possibly damaging |
Het |
Lrp1 |
T |
A |
10: 127,417,760 (GRCm39) |
|
probably null |
Het |
Ltbp4 |
T |
C |
7: 27,028,464 (GRCm39) |
N266S |
unknown |
Het |
Mgam |
G |
A |
6: 40,643,815 (GRCm39) |
S581N |
possibly damaging |
Het |
Mrgpra9 |
T |
A |
7: 46,885,386 (GRCm39) |
I94L |
probably benign |
Het |
Msantd4 |
A |
T |
9: 4,384,023 (GRCm39) |
I115F |
probably benign |
Het |
Nrxn1 |
A |
C |
17: 90,950,481 (GRCm39) |
L566R |
probably benign |
Het |
Or5p59 |
T |
A |
7: 107,702,822 (GRCm39) |
I102N |
probably benign |
Het |
Prl7d1 |
A |
T |
13: 27,893,180 (GRCm39) |
F243I |
possibly damaging |
Het |
Rbm27 |
T |
C |
18: 42,450,746 (GRCm39) |
S509P |
probably damaging |
Het |
Rnf44 |
C |
T |
13: 54,829,821 (GRCm39) |
E306K |
probably damaging |
Het |
Rp1 |
T |
C |
1: 4,416,520 (GRCm39) |
R1531G |
possibly damaging |
Het |
Sf3b4 |
A |
G |
3: 96,080,953 (GRCm39) |
|
probably null |
Het |
Sfi1 |
TCGC |
TC |
11: 3,096,254 (GRCm39) |
|
probably null |
Het |
Sfi1 |
CCTCTC |
CCTCTCTC |
11: 3,127,419 (GRCm39) |
|
probably benign |
Het |
Sp110 |
T |
G |
1: 85,506,800 (GRCm39) |
E421A |
probably benign |
Het |
Stk4 |
C |
T |
2: 163,942,448 (GRCm39) |
T360M |
probably benign |
Het |
Vcan |
T |
A |
13: 89,836,603 (GRCm39) |
E2980D |
probably benign |
Het |
Vwa2 |
C |
T |
19: 56,869,570 (GRCm39) |
P2S |
unknown |
Het |
Wdr77 |
G |
A |
3: 105,874,573 (GRCm39) |
V322I |
possibly damaging |
Het |
Zfp12 |
C |
A |
5: 143,230,535 (GRCm39) |
Y287* |
probably null |
Het |
Zfp937 |
T |
A |
2: 150,080,868 (GRCm39) |
Y299* |
probably null |
Het |
|
Other mutations in Hspg2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00089:Hspg2
|
APN |
4 |
137,256,131 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00339:Hspg2
|
APN |
4 |
137,266,506 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00943:Hspg2
|
APN |
4 |
137,289,512 (GRCm39) |
missense |
probably benign |
0.15 |
IGL00970:Hspg2
|
APN |
4 |
137,269,901 (GRCm39) |
missense |
probably benign |
0.09 |
IGL01011:Hspg2
|
APN |
4 |
137,286,646 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01148:Hspg2
|
APN |
4 |
137,273,969 (GRCm39) |
missense |
probably benign |
0.11 |
IGL01333:Hspg2
|
APN |
4 |
137,267,625 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01367:Hspg2
|
APN |
4 |
137,265,800 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01455:Hspg2
|
APN |
4 |
137,281,128 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01540:Hspg2
|
APN |
4 |
137,247,017 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01578:Hspg2
|
APN |
4 |
137,266,494 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01603:Hspg2
|
APN |
4 |
137,280,114 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01632:Hspg2
|
APN |
4 |
137,242,084 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01658:Hspg2
|
APN |
4 |
137,292,237 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01760:Hspg2
|
APN |
4 |
137,239,982 (GRCm39) |
missense |
possibly damaging |
0.60 |
IGL01976:Hspg2
|
APN |
4 |
137,289,237 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02024:Hspg2
|
APN |
4 |
137,267,384 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02033:Hspg2
|
APN |
4 |
137,279,565 (GRCm39) |
missense |
probably benign |
|
IGL02051:Hspg2
|
APN |
4 |
137,295,700 (GRCm39) |
unclassified |
probably benign |
|
IGL02124:Hspg2
|
APN |
4 |
137,246,125 (GRCm39) |
splice site |
probably null |
|
IGL02128:Hspg2
|
APN |
4 |
137,291,327 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02177:Hspg2
|
APN |
4 |
137,242,627 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02230:Hspg2
|
APN |
4 |
137,245,956 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02266:Hspg2
|
APN |
4 |
137,237,888 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02313:Hspg2
|
APN |
4 |
137,235,700 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02477:Hspg2
|
APN |
4 |
137,271,823 (GRCm39) |
splice site |
probably benign |
|
IGL02514:Hspg2
|
APN |
4 |
137,296,887 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02613:Hspg2
|
APN |
4 |
137,271,731 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02625:Hspg2
|
APN |
4 |
137,239,953 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02646:Hspg2
|
APN |
4 |
137,279,159 (GRCm39) |
missense |
possibly damaging |
0.60 |
IGL02651:Hspg2
|
APN |
4 |
137,284,756 (GRCm39) |
splice site |
probably benign |
|
IGL02701:Hspg2
|
APN |
4 |
137,284,485 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02833:Hspg2
|
APN |
4 |
137,282,441 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02985:Hspg2
|
APN |
4 |
137,235,114 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03040:Hspg2
|
APN |
4 |
137,289,136 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03181:Hspg2
|
APN |
4 |
137,243,248 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03349:Hspg2
|
APN |
4 |
137,287,833 (GRCm39) |
splice site |
probably benign |
|
G1patch:Hspg2
|
UTSW |
4 |
137,242,618 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4305001:Hspg2
|
UTSW |
4 |
137,277,684 (GRCm39) |
missense |
possibly damaging |
0.55 |
R0006:Hspg2
|
UTSW |
4 |
137,247,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R0036:Hspg2
|
UTSW |
4 |
137,270,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R0109:Hspg2
|
UTSW |
4 |
137,289,512 (GRCm39) |
missense |
probably benign |
0.15 |
R0131:Hspg2
|
UTSW |
4 |
137,279,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R0131:Hspg2
|
UTSW |
4 |
137,279,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R0132:Hspg2
|
UTSW |
4 |
137,279,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R0245:Hspg2
|
UTSW |
4 |
137,242,033 (GRCm39) |
missense |
probably damaging |
1.00 |
R0388:Hspg2
|
UTSW |
4 |
137,238,469 (GRCm39) |
missense |
probably damaging |
1.00 |
R0389:Hspg2
|
UTSW |
4 |
137,242,734 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0468:Hspg2
|
UTSW |
4 |
137,260,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R0480:Hspg2
|
UTSW |
4 |
137,277,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R0546:Hspg2
|
UTSW |
4 |
137,229,605 (GRCm39) |
missense |
probably benign |
|
R0599:Hspg2
|
UTSW |
4 |
137,239,712 (GRCm39) |
missense |
probably damaging |
0.98 |
R0652:Hspg2
|
UTSW |
4 |
137,242,033 (GRCm39) |
missense |
probably damaging |
1.00 |
R0671:Hspg2
|
UTSW |
4 |
137,280,591 (GRCm39) |
missense |
probably damaging |
1.00 |
R0760:Hspg2
|
UTSW |
4 |
137,239,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R0883:Hspg2
|
UTSW |
4 |
137,268,751 (GRCm39) |
missense |
probably benign |
0.00 |
R1417:Hspg2
|
UTSW |
4 |
137,244,947 (GRCm39) |
missense |
probably benign |
|
R1497:Hspg2
|
UTSW |
4 |
137,275,407 (GRCm39) |
missense |
probably damaging |
0.98 |
R1509:Hspg2
|
UTSW |
4 |
137,238,552 (GRCm39) |
splice site |
probably benign |
|
R1625:Hspg2
|
UTSW |
4 |
137,246,282 (GRCm39) |
missense |
probably benign |
0.23 |
R1630:Hspg2
|
UTSW |
4 |
137,245,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R1651:Hspg2
|
UTSW |
4 |
137,260,748 (GRCm39) |
nonsense |
probably null |
|
R1699:Hspg2
|
UTSW |
4 |
137,275,323 (GRCm39) |
splice site |
probably null |
|
R1703:Hspg2
|
UTSW |
4 |
137,286,462 (GRCm39) |
missense |
probably damaging |
1.00 |
R1761:Hspg2
|
UTSW |
4 |
137,241,984 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1775:Hspg2
|
UTSW |
4 |
137,247,467 (GRCm39) |
missense |
probably damaging |
0.99 |
R1779:Hspg2
|
UTSW |
4 |
137,245,820 (GRCm39) |
missense |
probably damaging |
1.00 |
R1843:Hspg2
|
UTSW |
4 |
137,272,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R1891:Hspg2
|
UTSW |
4 |
137,292,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R1930:Hspg2
|
UTSW |
4 |
137,267,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R1931:Hspg2
|
UTSW |
4 |
137,267,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R1942:Hspg2
|
UTSW |
4 |
137,269,863 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1959:Hspg2
|
UTSW |
4 |
137,292,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R2042:Hspg2
|
UTSW |
4 |
137,295,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R2062:Hspg2
|
UTSW |
4 |
137,286,678 (GRCm39) |
missense |
possibly damaging |
0.79 |
R2098:Hspg2
|
UTSW |
4 |
137,247,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R2158:Hspg2
|
UTSW |
4 |
137,244,915 (GRCm39) |
missense |
probably damaging |
1.00 |
R2280:Hspg2
|
UTSW |
4 |
137,249,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R2890:Hspg2
|
UTSW |
4 |
137,276,885 (GRCm39) |
missense |
probably damaging |
1.00 |
R2927:Hspg2
|
UTSW |
4 |
137,246,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R3428:Hspg2
|
UTSW |
4 |
137,282,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R3744:Hspg2
|
UTSW |
4 |
137,292,815 (GRCm39) |
splice site |
probably benign |
|
R3873:Hspg2
|
UTSW |
4 |
137,266,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R3874:Hspg2
|
UTSW |
4 |
137,266,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R3917:Hspg2
|
UTSW |
4 |
137,286,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R3932:Hspg2
|
UTSW |
4 |
137,242,879 (GRCm39) |
missense |
probably damaging |
0.99 |
R3933:Hspg2
|
UTSW |
4 |
137,242,879 (GRCm39) |
missense |
probably damaging |
0.99 |
R4134:Hspg2
|
UTSW |
4 |
137,283,968 (GRCm39) |
missense |
probably damaging |
0.99 |
R4272:Hspg2
|
UTSW |
4 |
137,246,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R4273:Hspg2
|
UTSW |
4 |
137,246,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R4274:Hspg2
|
UTSW |
4 |
137,246,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R4275:Hspg2
|
UTSW |
4 |
137,246,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R4288:Hspg2
|
UTSW |
4 |
137,246,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R4289:Hspg2
|
UTSW |
4 |
137,246,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R4354:Hspg2
|
UTSW |
4 |
137,196,222 (GRCm39) |
missense |
probably benign |
0.17 |
R4355:Hspg2
|
UTSW |
4 |
137,256,729 (GRCm39) |
missense |
probably damaging |
0.98 |
R4400:Hspg2
|
UTSW |
4 |
137,275,433 (GRCm39) |
missense |
probably benign |
0.01 |
R4411:Hspg2
|
UTSW |
4 |
137,289,535 (GRCm39) |
missense |
probably benign |
|
R4421:Hspg2
|
UTSW |
4 |
137,275,433 (GRCm39) |
missense |
probably benign |
0.01 |
R4592:Hspg2
|
UTSW |
4 |
137,246,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R4612:Hspg2
|
UTSW |
4 |
137,266,886 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4612:Hspg2
|
UTSW |
4 |
137,246,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R4619:Hspg2
|
UTSW |
4 |
137,273,884 (GRCm39) |
missense |
probably damaging |
1.00 |
R4658:Hspg2
|
UTSW |
4 |
137,261,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R4667:Hspg2
|
UTSW |
4 |
137,266,956 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4724:Hspg2
|
UTSW |
4 |
137,249,438 (GRCm39) |
missense |
probably damaging |
0.96 |
R4739:Hspg2
|
UTSW |
4 |
137,297,384 (GRCm39) |
unclassified |
probably benign |
|
R4793:Hspg2
|
UTSW |
4 |
137,256,784 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4826:Hspg2
|
UTSW |
4 |
137,292,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R4838:Hspg2
|
UTSW |
4 |
137,268,977 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4896:Hspg2
|
UTSW |
4 |
137,246,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R4926:Hspg2
|
UTSW |
4 |
137,269,841 (GRCm39) |
missense |
probably damaging |
1.00 |
R4939:Hspg2
|
UTSW |
4 |
137,235,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R5032:Hspg2
|
UTSW |
4 |
137,246,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R5033:Hspg2
|
UTSW |
4 |
137,246,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R5071:Hspg2
|
UTSW |
4 |
137,267,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R5072:Hspg2
|
UTSW |
4 |
137,267,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R5114:Hspg2
|
UTSW |
4 |
137,239,237 (GRCm39) |
missense |
probably damaging |
1.00 |
R5177:Hspg2
|
UTSW |
4 |
137,246,083 (GRCm39) |
missense |
probably damaging |
1.00 |
R5223:Hspg2
|
UTSW |
4 |
137,271,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R5433:Hspg2
|
UTSW |
4 |
137,256,105 (GRCm39) |
splice site |
probably null |
|
R5529:Hspg2
|
UTSW |
4 |
137,279,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R5541:Hspg2
|
UTSW |
4 |
137,270,136 (GRCm39) |
missense |
probably benign |
0.17 |
R5541:Hspg2
|
UTSW |
4 |
137,247,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R5546:Hspg2
|
UTSW |
4 |
137,275,485 (GRCm39) |
critical splice donor site |
probably null |
|
R5728:Hspg2
|
UTSW |
4 |
137,270,077 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5764:Hspg2
|
UTSW |
4 |
137,289,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R5920:Hspg2
|
UTSW |
4 |
137,281,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R5934:Hspg2
|
UTSW |
4 |
137,246,083 (GRCm39) |
missense |
probably damaging |
1.00 |
R6074:Hspg2
|
UTSW |
4 |
137,268,046 (GRCm39) |
missense |
probably benign |
|
R6164:Hspg2
|
UTSW |
4 |
137,241,966 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6175:Hspg2
|
UTSW |
4 |
137,296,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R6217:Hspg2
|
UTSW |
4 |
137,267,559 (GRCm39) |
missense |
probably damaging |
0.99 |
R6262:Hspg2
|
UTSW |
4 |
137,246,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R6299:Hspg2
|
UTSW |
4 |
137,272,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R6333:Hspg2
|
UTSW |
4 |
137,289,266 (GRCm39) |
missense |
probably damaging |
1.00 |
R6371:Hspg2
|
UTSW |
4 |
137,269,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R6430:Hspg2
|
UTSW |
4 |
137,266,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R6498:Hspg2
|
UTSW |
4 |
137,235,112 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6522:Hspg2
|
UTSW |
4 |
137,282,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R6680:Hspg2
|
UTSW |
4 |
137,293,048 (GRCm39) |
missense |
probably benign |
0.18 |
R6724:Hspg2
|
UTSW |
4 |
137,242,618 (GRCm39) |
missense |
probably damaging |
1.00 |
R6725:Hspg2
|
UTSW |
4 |
137,242,618 (GRCm39) |
missense |
probably damaging |
1.00 |
R6762:Hspg2
|
UTSW |
4 |
137,279,114 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6785:Hspg2
|
UTSW |
4 |
137,235,709 (GRCm39) |
missense |
probably damaging |
0.99 |
R6788:Hspg2
|
UTSW |
4 |
137,242,618 (GRCm39) |
missense |
probably damaging |
1.00 |
R6931:Hspg2
|
UTSW |
4 |
137,268,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R6959:Hspg2
|
UTSW |
4 |
137,246,600 (GRCm39) |
missense |
probably benign |
0.45 |
R6968:Hspg2
|
UTSW |
4 |
137,262,467 (GRCm39) |
missense |
probably damaging |
1.00 |
R6988:Hspg2
|
UTSW |
4 |
137,256,201 (GRCm39) |
missense |
probably damaging |
1.00 |
R7021:Hspg2
|
UTSW |
4 |
137,269,580 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7089:Hspg2
|
UTSW |
4 |
137,271,677 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7107:Hspg2
|
UTSW |
4 |
137,237,963 (GRCm39) |
missense |
probably damaging |
1.00 |
R7141:Hspg2
|
UTSW |
4 |
137,279,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R7161:Hspg2
|
UTSW |
4 |
137,242,030 (GRCm39) |
missense |
probably damaging |
1.00 |
R7189:Hspg2
|
UTSW |
4 |
137,260,872 (GRCm39) |
critical splice donor site |
probably null |
|
R7238:Hspg2
|
UTSW |
4 |
137,235,704 (GRCm39) |
missense |
probably damaging |
1.00 |
R7253:Hspg2
|
UTSW |
4 |
137,247,257 (GRCm39) |
missense |
probably benign |
0.15 |
R7278:Hspg2
|
UTSW |
4 |
137,278,436 (GRCm39) |
missense |
probably damaging |
0.98 |
R7287:Hspg2
|
UTSW |
4 |
137,256,867 (GRCm39) |
missense |
probably benign |
0.00 |
R7390:Hspg2
|
UTSW |
4 |
137,266,490 (GRCm39) |
missense |
probably damaging |
1.00 |
R7436:Hspg2
|
UTSW |
4 |
137,242,975 (GRCm39) |
missense |
probably damaging |
0.99 |
R7479:Hspg2
|
UTSW |
4 |
137,266,714 (GRCm39) |
missense |
probably benign |
0.17 |
R7516:Hspg2
|
UTSW |
4 |
137,269,931 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7540:Hspg2
|
UTSW |
4 |
137,268,751 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7603:Hspg2
|
UTSW |
4 |
137,284,503 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7603:Hspg2
|
UTSW |
4 |
137,275,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R7625:Hspg2
|
UTSW |
4 |
137,292,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R7696:Hspg2
|
UTSW |
4 |
137,239,277 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7767:Hspg2
|
UTSW |
4 |
137,239,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R7815:Hspg2
|
UTSW |
4 |
137,239,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R7825:Hspg2
|
UTSW |
4 |
137,286,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R7863:Hspg2
|
UTSW |
4 |
137,292,135 (GRCm39) |
missense |
probably benign |
0.03 |
R7885:Hspg2
|
UTSW |
4 |
137,244,148 (GRCm39) |
missense |
probably damaging |
1.00 |
R7899:Hspg2
|
UTSW |
4 |
137,275,427 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7937:Hspg2
|
UTSW |
4 |
137,278,243 (GRCm39) |
missense |
probably benign |
0.01 |
R7975:Hspg2
|
UTSW |
4 |
137,282,532 (GRCm39) |
missense |
probably benign |
0.26 |
R8078:Hspg2
|
UTSW |
4 |
137,235,333 (GRCm39) |
missense |
probably damaging |
1.00 |
R8285:Hspg2
|
UTSW |
4 |
137,239,974 (GRCm39) |
missense |
probably benign |
0.18 |
R8314:Hspg2
|
UTSW |
4 |
137,266,986 (GRCm39) |
missense |
probably benign |
0.12 |
R8322:Hspg2
|
UTSW |
4 |
137,246,290 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8323:Hspg2
|
UTSW |
4 |
137,246,290 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8324:Hspg2
|
UTSW |
4 |
137,246,290 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8341:Hspg2
|
UTSW |
4 |
137,246,290 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8383:Hspg2
|
UTSW |
4 |
137,271,681 (GRCm39) |
missense |
possibly damaging |
0.66 |
R8425:Hspg2
|
UTSW |
4 |
137,278,178 (GRCm39) |
nonsense |
probably null |
|
R8491:Hspg2
|
UTSW |
4 |
137,281,030 (GRCm39) |
missense |
probably benign |
0.00 |
R8525:Hspg2
|
UTSW |
4 |
137,266,759 (GRCm39) |
missense |
probably damaging |
0.98 |
R8978:Hspg2
|
UTSW |
4 |
137,291,341 (GRCm39) |
missense |
probably benign |
0.09 |
R9152:Hspg2
|
UTSW |
4 |
137,249,876 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9166:Hspg2
|
UTSW |
4 |
137,270,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R9175:Hspg2
|
UTSW |
4 |
137,256,657 (GRCm39) |
missense |
probably damaging |
0.98 |
R9210:Hspg2
|
UTSW |
4 |
137,289,790 (GRCm39) |
missense |
probably benign |
0.05 |
R9221:Hspg2
|
UTSW |
4 |
137,287,726 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9325:Hspg2
|
UTSW |
4 |
137,265,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R9339:Hspg2
|
UTSW |
4 |
137,278,480 (GRCm39) |
missense |
probably benign |
|
R9340:Hspg2
|
UTSW |
4 |
137,296,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R9358:Hspg2
|
UTSW |
4 |
137,244,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R9451:Hspg2
|
UTSW |
4 |
137,238,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R9534:Hspg2
|
UTSW |
4 |
137,268,072 (GRCm39) |
missense |
probably benign |
|
R9656:Hspg2
|
UTSW |
4 |
137,279,196 (GRCm39) |
missense |
probably benign |
|
R9664:Hspg2
|
UTSW |
4 |
137,266,887 (GRCm39) |
missense |
probably benign |
0.03 |
R9695:Hspg2
|
UTSW |
4 |
137,265,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R9741:Hspg2
|
UTSW |
4 |
137,239,962 (GRCm39) |
missense |
probably damaging |
1.00 |
V5622:Hspg2
|
UTSW |
4 |
137,261,049 (GRCm39) |
missense |
probably damaging |
0.99 |
V5622:Hspg2
|
UTSW |
4 |
137,261,049 (GRCm39) |
missense |
probably damaging |
0.99 |
X0028:Hspg2
|
UTSW |
4 |
137,277,702 (GRCm39) |
missense |
probably benign |
|
Z1177:Hspg2
|
UTSW |
4 |
137,295,684 (GRCm39) |
missense |
possibly damaging |
0.64 |
Z1177:Hspg2
|
UTSW |
4 |
137,291,829 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Hspg2
|
UTSW |
4 |
137,277,778 (GRCm39) |
missense |
probably damaging |
1.00 |
|