Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc12 |
A |
G |
8: 87,258,197 (GRCm39) |
I773T |
probably benign |
Het |
Adamtsl1 |
T |
A |
4: 86,260,960 (GRCm39) |
I1057N |
possibly damaging |
Het |
Anxa5 |
G |
A |
3: 36,504,821 (GRCm39) |
A247V |
probably damaging |
Het |
Ascc3 |
T |
G |
10: 50,611,425 (GRCm39) |
W1589G |
probably damaging |
Het |
Atp2b2 |
G |
A |
6: 113,770,743 (GRCm39) |
P389S |
probably damaging |
Het |
Bpifa6 |
T |
A |
2: 153,824,851 (GRCm39) |
S9T |
probably benign |
Het |
Cfhr4 |
T |
A |
1: 139,682,009 (GRCm39) |
T196S |
probably damaging |
Het |
Chd8 |
A |
G |
14: 52,442,783 (GRCm39) |
V589A |
probably benign |
Het |
Chrnb2 |
T |
C |
3: 89,671,713 (GRCm39) |
M1V |
probably null |
Het |
Col16a1 |
T |
A |
4: 129,960,889 (GRCm39) |
V449E |
unknown |
Het |
Cttnbp2nl |
T |
G |
3: 104,913,173 (GRCm39) |
K237T |
probably damaging |
Het |
Dazap1 |
T |
G |
10: 80,114,060 (GRCm39) |
|
probably null |
Het |
Fam187b |
T |
A |
7: 30,688,545 (GRCm39) |
V22E |
probably damaging |
Het |
Fat2 |
A |
T |
11: 55,164,037 (GRCm39) |
S3073T |
probably benign |
Het |
Fcgbpl1 |
A |
G |
7: 27,837,040 (GRCm39) |
R320G |
probably damaging |
Het |
Gm16069 |
T |
C |
3: 89,088,232 (GRCm39) |
|
probably benign |
Het |
H2-T24 |
T |
A |
17: 36,325,878 (GRCm39) |
I238F |
probably damaging |
Het |
Hectd4 |
A |
G |
5: 121,471,087 (GRCm39) |
E2658G |
probably benign |
Het |
Herc1 |
A |
C |
9: 66,388,192 (GRCm39) |
I3826L |
probably benign |
Het |
Hinfp |
A |
G |
9: 44,211,060 (GRCm39) |
C67R |
probably damaging |
Het |
Hp1bp3 |
C |
T |
4: 137,964,520 (GRCm39) |
S348F |
probably damaging |
Het |
Htr1f |
A |
G |
16: 64,747,091 (GRCm39) |
V67A |
probably damaging |
Het |
Iqcc |
T |
G |
4: 129,510,392 (GRCm39) |
E374D |
probably damaging |
Het |
Kcnj9 |
T |
C |
1: 172,153,765 (GRCm39) |
T120A |
probably damaging |
Het |
Kif3a |
A |
G |
11: 53,477,743 (GRCm39) |
K404R |
possibly damaging |
Het |
Kitl |
C |
T |
10: 99,923,226 (GRCm39) |
P208S |
probably benign |
Het |
Lpcat4 |
A |
G |
2: 112,077,093 (GRCm39) |
Y479C |
probably damaging |
Het |
Lrrc74b |
T |
C |
16: 17,371,016 (GRCm39) |
N227S |
probably damaging |
Het |
Mdc1 |
T |
A |
17: 36,163,473 (GRCm39) |
V1007D |
probably damaging |
Het |
Mocos |
T |
G |
18: 24,812,819 (GRCm39) |
I571S |
probably benign |
Het |
Myh8 |
A |
G |
11: 67,183,014 (GRCm39) |
N659D |
probably damaging |
Het |
Naip2 |
A |
G |
13: 100,320,296 (GRCm39) |
V240A |
probably benign |
Het |
Nap1l1 |
T |
C |
10: 111,321,370 (GRCm39) |
S37P |
probably benign |
Het |
Nin |
T |
G |
12: 70,097,915 (GRCm39) |
K515T |
probably damaging |
Het |
Npl |
T |
A |
1: 153,384,864 (GRCm39) |
K258* |
probably null |
Het |
Ntn4 |
T |
A |
10: 93,480,569 (GRCm39) |
S98T |
possibly damaging |
Het |
Or10x1 |
T |
C |
1: 174,197,152 (GRCm39) |
V223A |
probably damaging |
Het |
Or2z8 |
C |
T |
8: 72,812,244 (GRCm39) |
T240M |
probably damaging |
Het |
Or5k14 |
C |
A |
16: 58,693,269 (GRCm39) |
M81I |
probably benign |
Het |
Or8u10 |
T |
C |
2: 85,915,844 (GRCm39) |
I92M |
probably damaging |
Het |
Pkp2 |
T |
C |
16: 16,058,577 (GRCm39) |
|
probably benign |
Het |
Ppox |
C |
A |
1: 171,106,849 (GRCm39) |
A192S |
possibly damaging |
Het |
Prkdc |
T |
C |
16: 15,531,517 (GRCm39) |
L1380S |
probably benign |
Het |
Psd4 |
C |
A |
2: 24,295,363 (GRCm39) |
A839E |
probably damaging |
Het |
Ptprn2 |
T |
G |
12: 116,685,711 (GRCm39) |
F57V |
probably damaging |
Het |
Ptprt |
C |
T |
2: 162,120,030 (GRCm39) |
V146I |
probably benign |
Het |
R3hdm2 |
T |
A |
10: 127,334,322 (GRCm39) |
M915K |
probably damaging |
Het |
Rab26 |
C |
T |
17: 24,749,759 (GRCm39) |
|
probably null |
Het |
Rnf213 |
A |
G |
11: 119,321,187 (GRCm39) |
E1215G |
probably benign |
Het |
Rprd2 |
T |
C |
3: 95,681,673 (GRCm39) |
K407E |
probably damaging |
Het |
Siah3 |
G |
A |
14: 75,693,574 (GRCm39) |
V27I |
possibly damaging |
Het |
Slc14a2 |
T |
A |
18: 78,235,338 (GRCm39) |
N280Y |
probably damaging |
Het |
Slc17a3 |
C |
T |
13: 24,039,841 (GRCm39) |
S293F |
probably damaging |
Het |
Slc25a35 |
A |
G |
11: 68,862,786 (GRCm39) |
Y247C |
probably damaging |
Het |
Slc29a4 |
A |
G |
5: 142,691,285 (GRCm39) |
D55G |
probably benign |
Het |
Slc35d1 |
C |
T |
4: 103,065,378 (GRCm39) |
V189I |
probably benign |
Het |
Srrm1 |
G |
A |
4: 135,067,884 (GRCm39) |
R322* |
probably null |
Het |
Stac3 |
A |
T |
10: 127,339,519 (GRCm39) |
R138S |
probably damaging |
Het |
Tbc1d9b |
T |
C |
11: 50,026,751 (GRCm39) |
I73T |
probably benign |
Het |
Tgtp1 |
A |
G |
11: 48,878,159 (GRCm39) |
F182S |
probably benign |
Het |
Tmcc3 |
T |
C |
10: 94,381,437 (GRCm39) |
|
probably benign |
Het |
Tmem116 |
A |
G |
5: 121,631,845 (GRCm39) |
|
probably benign |
Het |
Tmem260 |
T |
A |
14: 48,720,779 (GRCm39) |
C306* |
probably null |
Het |
Tspyl1 |
A |
G |
10: 34,159,085 (GRCm39) |
N270S |
probably damaging |
Het |
Tusc1 |
A |
T |
4: 93,223,070 (GRCm39) |
H196Q |
probably benign |
Het |
Ugt2a1 |
T |
A |
5: 87,622,720 (GRCm39) |
K293* |
probably null |
Het |
Vmn2r102 |
A |
C |
17: 19,899,025 (GRCm39) |
T456P |
probably benign |
Het |
Vmn2r90 |
T |
A |
17: 17,932,511 (GRCm39) |
S139R |
probably benign |
Het |
Zfp879 |
C |
A |
11: 50,724,426 (GRCm39) |
G210V |
probably damaging |
Het |
Zmym2 |
A |
G |
14: 57,180,715 (GRCm39) |
N876D |
probably benign |
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 |
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 |
R1403:Hspg2
|
UTSW |
4 |
137,267,411 (GRCm39) |
missense |
possibly damaging |
0.90 |
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 |
|