Other mutations in this stock |
Total: 115 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700067K01Rik |
T |
C |
8: 84,729,637 (GRCm39) |
|
probably benign |
Het |
A530064D06Rik |
G |
A |
17: 48,473,824 (GRCm39) |
T31I |
probably benign |
Het |
Abca17 |
A |
G |
17: 24,500,223 (GRCm39) |
F1323L |
probably benign |
Het |
Abcf3 |
T |
A |
16: 20,369,237 (GRCm39) |
N206K |
probably damaging |
Het |
Adam10 |
A |
G |
9: 70,673,223 (GRCm39) |
|
probably benign |
Het |
Adamtsl3 |
A |
T |
7: 82,172,390 (GRCm39) |
Q451L |
probably damaging |
Het |
Adgrl3 |
T |
A |
5: 81,708,752 (GRCm39) |
I413N |
probably benign |
Het |
Asb18 |
G |
T |
1: 89,920,893 (GRCm39) |
A128E |
probably damaging |
Het |
Atf7ip2 |
T |
C |
16: 10,059,743 (GRCm39) |
S428P |
possibly damaging |
Het |
Atp8b5 |
G |
T |
4: 43,291,672 (GRCm39) |
C15F |
possibly damaging |
Het |
Bahcc1 |
A |
G |
11: 120,178,146 (GRCm39) |
E2235G |
probably damaging |
Het |
Blnk |
G |
T |
19: 40,926,111 (GRCm39) |
S330* |
probably null |
Het |
Bpnt1 |
T |
G |
1: 185,088,808 (GRCm39) |
N319K |
probably benign |
Het |
Brip1 |
G |
A |
11: 86,043,493 (GRCm39) |
T357I |
possibly damaging |
Het |
Cadm1 |
T |
A |
9: 47,725,104 (GRCm39) |
D288E |
probably benign |
Het |
Calcoco2 |
A |
G |
11: 95,998,354 (GRCm39) |
V23A |
probably damaging |
Het |
Cand2 |
G |
A |
6: 115,780,766 (GRCm39) |
E1217K |
probably damaging |
Het |
Ccdc154 |
G |
T |
17: 25,386,259 (GRCm39) |
|
probably benign |
Het |
Cdk12 |
T |
C |
11: 98,120,935 (GRCm39) |
|
probably benign |
Het |
Clec4a3 |
A |
G |
6: 122,930,993 (GRCm39) |
|
probably null |
Het |
Cpne2 |
T |
A |
8: 95,274,970 (GRCm39) |
|
probably benign |
Het |
Cyfip1 |
T |
C |
7: 55,573,710 (GRCm39) |
|
probably null |
Het |
Cyp26c1 |
A |
G |
19: 37,675,009 (GRCm39) |
H110R |
probably damaging |
Het |
Cyp2j13 |
A |
G |
4: 95,959,932 (GRCm39) |
Y75H |
probably damaging |
Het |
Defb43 |
T |
A |
14: 63,249,287 (GRCm39) |
V10D |
probably damaging |
Het |
Dhx36 |
G |
A |
3: 62,401,162 (GRCm39) |
S368L |
possibly damaging |
Het |
Dock6 |
G |
A |
9: 21,715,923 (GRCm39) |
|
probably benign |
Het |
Elp2 |
T |
C |
18: 24,745,499 (GRCm39) |
|
probably benign |
Het |
Emilin3 |
A |
G |
2: 160,750,249 (GRCm39) |
L453P |
probably damaging |
Het |
Eml6 |
A |
T |
11: 29,755,065 (GRCm39) |
D903E |
probably benign |
Het |
Ep300 |
T |
C |
15: 81,500,335 (GRCm39) |
|
probably benign |
Het |
Ep400 |
G |
A |
5: 110,836,062 (GRCm39) |
T1899M |
unknown |
Het |
Fancg |
A |
G |
4: 43,002,998 (GRCm39) |
S620P |
probably benign |
Het |
Fbxo42 |
G |
A |
4: 140,922,550 (GRCm39) |
V239M |
probably damaging |
Het |
Fermt2 |
T |
C |
14: 45,706,776 (GRCm39) |
D340G |
probably benign |
Het |
Filip1 |
A |
T |
9: 79,726,672 (GRCm39) |
V649E |
probably damaging |
Het |
Fut8 |
G |
A |
12: 77,521,791 (GRCm39) |
E477K |
probably damaging |
Het |
Gbp3 |
G |
A |
3: 142,271,151 (GRCm39) |
G185D |
probably benign |
Het |
Gclc |
G |
T |
9: 77,694,080 (GRCm39) |
D345Y |
probably damaging |
Het |
Gfus |
A |
G |
15: 75,800,807 (GRCm39) |
V27A |
possibly damaging |
Het |
Gkn2 |
A |
G |
6: 87,352,800 (GRCm39) |
D43G |
possibly damaging |
Het |
Gnptab |
A |
G |
10: 88,279,166 (GRCm39) |
|
probably benign |
Het |
Greb1l |
C |
T |
18: 10,474,303 (GRCm39) |
T206I |
probably damaging |
Het |
Grk4 |
A |
G |
5: 34,905,611 (GRCm39) |
N452S |
probably benign |
Het |
Hcn2 |
G |
C |
10: 79,570,066 (GRCm39) |
|
probably null |
Het |
Hpn |
T |
C |
7: 30,808,585 (GRCm39) |
K76E |
possibly damaging |
Het |
Immt |
A |
T |
6: 71,848,541 (GRCm39) |
Q467L |
possibly damaging |
Het |
Kalrn |
T |
C |
16: 33,936,778 (GRCm39) |
S1636G |
probably benign |
Het |
Kcnh8 |
T |
A |
17: 53,285,141 (GRCm39) |
L1037* |
probably null |
Het |
Klhl33 |
T |
C |
14: 51,129,851 (GRCm39) |
T548A |
probably damaging |
Het |
Klri2 |
T |
C |
6: 129,717,171 (GRCm39) |
I71V |
probably benign |
Het |
Kmt2c |
A |
T |
5: 25,609,363 (GRCm39) |
C254S |
probably damaging |
Het |
Lama3 |
T |
C |
18: 12,610,647 (GRCm39) |
I1170T |
possibly damaging |
Het |
Med12l |
A |
G |
3: 59,172,350 (GRCm39) |
Q1702R |
probably damaging |
Het |
Mga |
A |
T |
2: 119,750,391 (GRCm39) |
|
probably null |
Het |
Mis18a |
A |
T |
16: 90,517,561 (GRCm39) |
I172K |
possibly damaging |
Het |
Mrgpre |
T |
C |
7: 143,335,254 (GRCm39) |
D83G |
probably benign |
Het |
Mroh2a |
C |
A |
1: 88,170,142 (GRCm39) |
A685D |
possibly damaging |
Het |
Mrpl39 |
T |
C |
16: 84,531,282 (GRCm39) |
|
probably benign |
Het |
Mrrf |
C |
T |
2: 36,043,710 (GRCm39) |
A149V |
probably benign |
Het |
Mycbp2 |
A |
T |
14: 103,432,024 (GRCm39) |
M2338K |
possibly damaging |
Het |
Myo18b |
T |
C |
5: 112,840,632 (GRCm39) |
Q2387R |
probably benign |
Het |
N4bp2 |
T |
C |
5: 65,964,780 (GRCm39) |
I943T |
probably damaging |
Het |
Ncapd3 |
T |
A |
9: 26,998,773 (GRCm39) |
N1254K |
probably benign |
Het |
Ncoa1 |
A |
T |
12: 4,299,758 (GRCm39) |
|
probably null |
Het |
Ncor2 |
C |
T |
5: 125,126,451 (GRCm39) |
A136T |
probably benign |
Het |
Opa1 |
T |
C |
16: 29,421,025 (GRCm39) |
|
probably benign |
Het |
Or13a25 |
A |
G |
7: 140,247,590 (GRCm39) |
D123G |
probably damaging |
Het |
Or5p59 |
C |
A |
7: 107,703,363 (GRCm39) |
Y282* |
probably null |
Het |
Or8b39 |
T |
A |
9: 37,996,423 (GRCm39) |
M97K |
possibly damaging |
Het |
Or9e1 |
T |
A |
11: 58,732,681 (GRCm39) |
I247N |
possibly damaging |
Het |
Pcdhb4 |
T |
C |
18: 37,440,795 (GRCm39) |
M35T |
probably benign |
Het |
Per3 |
T |
C |
4: 151,113,288 (GRCm39) |
I347V |
probably benign |
Het |
Pex13 |
G |
A |
11: 23,615,831 (GRCm39) |
P5L |
possibly damaging |
Het |
Phkb |
T |
A |
8: 86,602,322 (GRCm39) |
W38R |
probably damaging |
Het |
Plekhf1 |
A |
T |
7: 37,920,826 (GRCm39) |
D247E |
probably benign |
Het |
Plxnb2 |
A |
G |
15: 89,042,184 (GRCm39) |
S1607P |
probably benign |
Het |
Plxnc1 |
T |
A |
10: 94,635,194 (GRCm39) |
H1344L |
possibly damaging |
Het |
Potefam1 |
A |
C |
2: 111,034,482 (GRCm39) |
V350G |
possibly damaging |
Het |
Ptk7 |
T |
G |
17: 46,901,238 (GRCm39) |
N196H |
possibly damaging |
Het |
Rab27a |
G |
T |
9: 72,982,715 (GRCm39) |
D7Y |
probably damaging |
Het |
Rars2 |
T |
A |
4: 34,630,505 (GRCm39) |
C82* |
probably null |
Het |
Rccd1 |
A |
T |
7: 79,969,965 (GRCm39) |
|
probably benign |
Het |
Riiad1 |
T |
C |
3: 94,379,546 (GRCm39) |
I56V |
possibly damaging |
Het |
Rnase4 |
A |
G |
14: 51,342,507 (GRCm39) |
E77G |
probably damaging |
Het |
Rnf126 |
A |
T |
10: 79,597,441 (GRCm39) |
I157N |
possibly damaging |
Het |
Rnf207 |
T |
C |
4: 152,391,925 (GRCm39) |
R623G |
probably benign |
Het |
Rpusd1 |
T |
G |
17: 25,947,498 (GRCm39) |
F62V |
possibly damaging |
Het |
Rxfp1 |
T |
C |
3: 79,570,600 (GRCm39) |
|
probably null |
Het |
Scfd1 |
A |
T |
12: 51,459,411 (GRCm39) |
Q324L |
probably benign |
Het |
Skint3 |
G |
T |
4: 112,112,974 (GRCm39) |
E195* |
probably null |
Het |
Slc7a10 |
A |
T |
7: 34,896,758 (GRCm39) |
T165S |
probably benign |
Het |
Smagp |
A |
G |
15: 100,519,733 (GRCm39) |
I97T |
probably damaging |
Het |
Sostdc1 |
A |
G |
12: 36,367,340 (GRCm39) |
H172R |
probably damaging |
Het |
Spast |
A |
G |
17: 74,646,446 (GRCm39) |
|
probably benign |
Het |
Sspo |
G |
T |
6: 48,467,325 (GRCm39) |
|
probably benign |
Het |
Ston2 |
C |
T |
12: 91,707,240 (GRCm39) |
|
probably null |
Het |
Tas2r103 |
T |
G |
6: 133,013,313 (GRCm39) |
E251A |
probably benign |
Het |
Tbc1d2b |
A |
T |
9: 90,104,558 (GRCm39) |
|
probably benign |
Het |
Telo2 |
G |
A |
17: 25,332,139 (GRCm39) |
P143L |
probably benign |
Het |
Tgfbi |
A |
T |
13: 56,786,539 (GRCm39) |
Y674F |
probably null |
Het |
Tha1 |
T |
A |
11: 117,763,983 (GRCm39) |
|
probably benign |
Het |
Timp4 |
T |
A |
6: 115,226,814 (GRCm39) |
S110C |
probably damaging |
Het |
Tlr6 |
T |
C |
5: 65,111,935 (GRCm39) |
K324R |
probably benign |
Het |
Tnip3 |
A |
G |
6: 65,574,347 (GRCm39) |
E137G |
probably damaging |
Het |
Top6bl |
A |
G |
19: 4,676,216 (GRCm39) |
S639P |
probably damaging |
Het |
Trak1 |
T |
C |
9: 121,278,021 (GRCm39) |
|
probably null |
Het |
Trim47 |
A |
G |
11: 115,999,178 (GRCm39) |
S233P |
probably benign |
Het |
Tspoap1 |
A |
T |
11: 87,653,635 (GRCm39) |
E155V |
probably damaging |
Het |
Uggt1 |
A |
T |
1: 36,194,209 (GRCm39) |
L1343Q |
probably damaging |
Het |
Utp14b |
T |
C |
1: 78,642,452 (GRCm39) |
S117P |
probably benign |
Het |
Vmn1r124 |
A |
T |
7: 20,994,436 (GRCm39) |
V36D |
probably damaging |
Het |
Wdr27 |
T |
C |
17: 15,148,658 (GRCm39) |
T112A |
probably benign |
Het |
Wdr90 |
T |
C |
17: 26,065,367 (GRCm39) |
T1630A |
probably benign |
Het |
Zfp352 |
A |
G |
4: 90,112,156 (GRCm39) |
T99A |
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 |
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 |
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 |
|