Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930447F04Rik |
T |
C |
X: 65,347,274 (GRCm39) |
E91G |
unknown |
Het |
Acot1 |
A |
G |
12: 84,064,113 (GRCm39) |
Q407R |
probably benign |
Het |
Adcy10 |
T |
A |
1: 165,398,297 (GRCm39) |
Y1465N |
probably damaging |
Het |
Ahsa2 |
T |
A |
11: 23,440,702 (GRCm39) |
I249F |
probably damaging |
Het |
Arhgap10 |
T |
C |
8: 77,977,594 (GRCm39) |
N721S |
probably damaging |
Het |
Arrdc4 |
T |
G |
7: 68,391,619 (GRCm39) |
E216A |
probably damaging |
Het |
Axin1 |
T |
C |
17: 26,392,637 (GRCm39) |
V306A |
probably benign |
Het |
Cct3 |
T |
C |
3: 88,210,173 (GRCm39) |
|
probably null |
Het |
Cfap58 |
G |
A |
19: 47,963,119 (GRCm39) |
|
probably null |
Het |
Chd9 |
T |
C |
8: 91,699,859 (GRCm39) |
S49P |
possibly damaging |
Het |
Clcn2 |
C |
A |
16: 20,529,178 (GRCm39) |
|
probably null |
Het |
Col26a1 |
T |
C |
5: 136,783,047 (GRCm39) |
N286D |
probably benign |
Het |
Cpt1b |
T |
A |
15: 89,308,596 (GRCm39) |
I111F |
possibly damaging |
Het |
Cyp4f16 |
T |
A |
17: 32,756,061 (GRCm39) |
I30N |
probably damaging |
Het |
Ddc |
T |
G |
11: 11,830,587 (GRCm39) |
D19A |
possibly damaging |
Het |
Depdc1a |
T |
A |
3: 159,222,537 (GRCm39) |
|
probably null |
Het |
Evc2 |
T |
A |
5: 37,574,828 (GRCm39) |
C1028S |
possibly damaging |
Het |
Fam228a |
T |
C |
12: 4,781,457 (GRCm39) |
E134G |
probably damaging |
Het |
Fasl |
T |
C |
1: 161,615,523 (GRCm39) |
E111G |
probably benign |
Het |
Fbxw10 |
A |
G |
11: 62,767,564 (GRCm39) |
N800S |
possibly damaging |
Het |
Fras1 |
T |
C |
5: 96,910,524 (GRCm39) |
S3318P |
probably damaging |
Het |
G3bp1 |
T |
C |
11: 55,389,452 (GRCm39) |
F383L |
probably damaging |
Het |
Gad1 |
T |
A |
2: 70,409,545 (GRCm39) |
M212K |
probably damaging |
Het |
Gm17455 |
T |
G |
10: 60,238,752 (GRCm39) |
S6A |
probably benign |
Het |
Grm5 |
T |
C |
7: 87,779,997 (GRCm39) |
S1146P |
probably damaging |
Het |
Gsn |
T |
C |
2: 35,194,651 (GRCm39) |
L649P |
probably damaging |
Het |
H2-DMb1 |
A |
G |
17: 34,374,685 (GRCm39) |
T112A |
probably benign |
Het |
Hcn3 |
T |
A |
3: 89,060,201 (GRCm39) |
I148F |
probably damaging |
Het |
Hdac10 |
T |
C |
15: 89,009,961 (GRCm39) |
|
probably null |
Het |
Hk3 |
C |
A |
13: 55,156,518 (GRCm39) |
D619Y |
probably damaging |
Het |
Ifi44 |
T |
A |
3: 151,451,134 (GRCm39) |
R272S |
possibly damaging |
Het |
Il1rap |
A |
C |
16: 26,517,625 (GRCm39) |
D275A |
probably damaging |
Het |
Irag2 |
A |
G |
6: 145,113,710 (GRCm39) |
R293G |
possibly damaging |
Het |
Itgam |
A |
T |
7: 127,707,152 (GRCm39) |
N660I |
probably benign |
Het |
Itpr3 |
T |
C |
17: 27,332,793 (GRCm39) |
M1853T |
probably benign |
Het |
Lrrc8c |
A |
C |
5: 105,754,965 (GRCm39) |
K247Q |
probably damaging |
Het |
Map3k21 |
T |
C |
8: 126,668,858 (GRCm39) |
S815P |
probably benign |
Het |
Mast4 |
A |
G |
13: 102,888,068 (GRCm39) |
S1114P |
probably damaging |
Het |
Myh8 |
C |
T |
11: 67,194,591 (GRCm39) |
Q1601* |
probably null |
Het |
Nhlrc2 |
A |
G |
19: 56,558,959 (GRCm39) |
D148G |
probably damaging |
Het |
Nos1 |
T |
A |
5: 118,081,385 (GRCm39) |
S1196T |
probably benign |
Het |
Nsmaf |
C |
T |
4: 6,424,874 (GRCm39) |
|
probably null |
Het |
Obscn |
T |
C |
11: 58,890,449 (GRCm39) |
D7361G |
unknown |
Het |
Or2t35 |
T |
C |
14: 14,407,777 (GRCm38) |
V183A |
probably damaging |
Het |
Or52ad1 |
C |
A |
7: 102,996,085 (GRCm39) |
A17S |
probably benign |
Het |
Or5bw2 |
C |
T |
7: 6,573,359 (GRCm39) |
A123V |
probably damaging |
Het |
Pank3 |
T |
G |
11: 35,668,536 (GRCm39) |
M175R |
probably benign |
Het |
Papolg |
A |
G |
11: 23,829,868 (GRCm39) |
|
probably null |
Het |
Pcdhb21 |
G |
A |
18: 37,647,566 (GRCm39) |
D232N |
probably damaging |
Het |
Pcdhb22 |
T |
C |
18: 37,651,925 (GRCm39) |
F131S |
probably damaging |
Het |
Pik3r6 |
G |
A |
11: 68,419,608 (GRCm39) |
A140T |
possibly damaging |
Het |
Pinlyp |
T |
C |
7: 24,241,947 (GRCm39) |
T87A |
possibly damaging |
Het |
Pld1 |
T |
C |
3: 28,178,724 (GRCm39) |
S873P |
probably damaging |
Het |
Pld5 |
T |
A |
1: 176,102,295 (GRCm39) |
Y49F |
probably benign |
Het |
Polq |
T |
C |
16: 36,855,252 (GRCm39) |
V449A |
probably damaging |
Het |
Prkca |
A |
G |
11: 107,869,106 (GRCm39) |
V69A |
probably benign |
Het |
Ptk6 |
A |
G |
2: 180,844,075 (GRCm39) |
S75P |
possibly damaging |
Het |
Ptprq |
G |
A |
10: 107,418,391 (GRCm39) |
Q1662* |
probably null |
Het |
Ptprt |
C |
A |
2: 161,395,742 (GRCm39) |
A1144S |
probably damaging |
Het |
Rrm1 |
T |
A |
7: 102,116,133 (GRCm39) |
W684R |
probably damaging |
Het |
Ryr1 |
T |
A |
7: 28,735,500 (GRCm39) |
M4093L |
probably damaging |
Het |
Scnn1a |
C |
T |
6: 125,299,189 (GRCm39) |
L90F |
probably damaging |
Het |
Slc25a19 |
G |
T |
11: 115,508,423 (GRCm39) |
Y188* |
probably null |
Het |
Slc31a1 |
C |
T |
4: 62,303,866 (GRCm39) |
|
probably benign |
Het |
Slc5a11 |
C |
G |
7: 122,864,458 (GRCm39) |
S351R |
possibly damaging |
Het |
Slc6a17 |
A |
G |
3: 107,384,183 (GRCm39) |
L387P |
probably benign |
Het |
Slitrk6 |
A |
T |
14: 110,987,364 (GRCm39) |
L781H |
probably damaging |
Het |
Spam1 |
T |
A |
6: 24,797,837 (GRCm39) |
L331Q |
probably damaging |
Het |
Spata32 |
A |
G |
11: 103,100,125 (GRCm39) |
W127R |
probably damaging |
Het |
Spring1 |
A |
G |
5: 118,393,886 (GRCm39) |
E88G |
possibly damaging |
Het |
St6galnac4 |
A |
G |
2: 32,484,330 (GRCm39) |
Y176C |
probably damaging |
Het |
Stk10 |
A |
G |
11: 32,546,724 (GRCm39) |
E327G |
probably damaging |
Het |
Stxbp5l |
T |
A |
16: 36,954,646 (GRCm39) |
Y912F |
possibly damaging |
Het |
Tchp |
G |
A |
5: 114,858,243 (GRCm39) |
E459K |
probably benign |
Het |
Terf2 |
C |
T |
8: 107,822,842 (GRCm39) |
W100* |
probably null |
Het |
Thoc2l |
T |
G |
5: 104,666,077 (GRCm39) |
S200A |
probably benign |
Het |
Thrsp |
T |
C |
7: 97,066,634 (GRCm39) |
N26S |
probably damaging |
Het |
Tln1 |
C |
A |
4: 43,553,504 (GRCm39) |
R297L |
probably benign |
Het |
Tmeff2 |
C |
A |
1: 50,967,234 (GRCm39) |
T43N |
possibly damaging |
Het |
Tmx1 |
C |
T |
12: 70,499,947 (GRCm39) |
A2V |
possibly damaging |
Het |
Tnks1bp1 |
T |
A |
2: 84,902,481 (GRCm39) |
L1053Q |
probably damaging |
Het |
Trmt10b |
A |
T |
4: 45,304,286 (GRCm39) |
K107N |
probably damaging |
Het |
Trpa1 |
A |
T |
1: 14,955,972 (GRCm39) |
|
probably null |
Het |
Trrap |
A |
G |
5: 144,783,287 (GRCm39) |
K3371R |
probably damaging |
Het |
Tuba3b |
G |
A |
6: 145,563,995 (GRCm39) |
V14I |
probably benign |
Het |
Usp19 |
T |
C |
9: 108,371,439 (GRCm39) |
|
probably null |
Het |
Usp28 |
C |
A |
9: 48,950,401 (GRCm39) |
D615E |
possibly damaging |
Het |
Utp20 |
T |
C |
10: 88,657,931 (GRCm39) |
D43G |
probably benign |
Het |
Vmn1r58 |
T |
G |
7: 5,413,997 (GRCm39) |
K78Q |
possibly damaging |
Het |
Vmn2r10 |
T |
C |
5: 109,151,327 (GRCm39) |
M96V |
probably benign |
Het |
Wdr90 |
T |
C |
17: 26,079,023 (GRCm39) |
E273G |
probably damaging |
Het |
Xpc |
C |
T |
6: 91,468,208 (GRCm39) |
A860T |
probably benign |
Het |
Zscan21 |
T |
C |
5: 138,131,865 (GRCm39) |
I463T |
possibly damaging |
Het |
|
Other mutations in Spta1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00979:Spta1
|
APN |
1 |
174,035,956 (GRCm39) |
nonsense |
probably null |
|
IGL01095:Spta1
|
APN |
1 |
174,041,051 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01144:Spta1
|
APN |
1 |
174,014,829 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01455:Spta1
|
APN |
1 |
174,030,877 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL01541:Spta1
|
APN |
1 |
174,044,725 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01613:Spta1
|
APN |
1 |
174,035,960 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01804:Spta1
|
APN |
1 |
174,071,746 (GRCm39) |
missense |
probably benign |
0.42 |
IGL01859:Spta1
|
APN |
1 |
174,001,938 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01898:Spta1
|
APN |
1 |
174,041,428 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02106:Spta1
|
APN |
1 |
174,030,860 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02166:Spta1
|
APN |
1 |
174,017,797 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02224:Spta1
|
APN |
1 |
174,045,255 (GRCm39) |
critical splice donor site |
probably benign |
|
IGL02318:Spta1
|
APN |
1 |
174,002,029 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL02392:Spta1
|
APN |
1 |
174,046,380 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02852:Spta1
|
APN |
1 |
174,071,676 (GRCm39) |
missense |
probably benign |
0.24 |
IGL02861:Spta1
|
APN |
1 |
174,039,164 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02982:Spta1
|
APN |
1 |
174,014,854 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03057:Spta1
|
APN |
1 |
174,008,624 (GRCm39) |
missense |
probably benign |
0.19 |
IGL03215:Spta1
|
APN |
1 |
174,046,309 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03263:Spta1
|
APN |
1 |
174,041,484 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03272:Spta1
|
APN |
1 |
174,041,710 (GRCm39) |
missense |
probably benign |
0.08 |
bounced
|
UTSW |
1 |
174,052,023 (GRCm39) |
missense |
probably damaging |
1.00 |
Capillus
|
UTSW |
1 |
174,045,254 (GRCm39) |
critical splice donor site |
probably null |
|
Deflection
|
UTSW |
1 |
174,068,653 (GRCm39) |
missense |
probably damaging |
1.00 |
Goldfoil
|
UTSW |
1 |
174,046,078 (GRCm39) |
missense |
probably damaging |
1.00 |
hanging
|
UTSW |
1 |
174,006,315 (GRCm39) |
missense |
probably damaging |
0.99 |
Klimt
|
UTSW |
1 |
174,029,952 (GRCm39) |
missense |
probably damaging |
1.00 |
Rutherford
|
UTSW |
1 |
174,034,676 (GRCm39) |
missense |
probably null |
1.00 |
Thread
|
UTSW |
1 |
174,025,201 (GRCm39) |
nonsense |
probably null |
|
H8786:Spta1
|
UTSW |
1 |
174,007,405 (GRCm39) |
missense |
probably damaging |
0.98 |
R0003:Spta1
|
UTSW |
1 |
174,032,839 (GRCm39) |
missense |
probably damaging |
0.98 |
R0003:Spta1
|
UTSW |
1 |
174,032,839 (GRCm39) |
missense |
probably damaging |
0.98 |
R0010:Spta1
|
UTSW |
1 |
174,045,509 (GRCm39) |
missense |
probably benign |
0.03 |
R0010:Spta1
|
UTSW |
1 |
174,045,509 (GRCm39) |
missense |
probably benign |
0.03 |
R0078:Spta1
|
UTSW |
1 |
174,034,598 (GRCm39) |
splice site |
probably benign |
|
R0172:Spta1
|
UTSW |
1 |
174,058,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R0206:Spta1
|
UTSW |
1 |
174,020,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R0208:Spta1
|
UTSW |
1 |
174,020,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R0276:Spta1
|
UTSW |
1 |
174,045,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R0288:Spta1
|
UTSW |
1 |
174,070,745 (GRCm39) |
missense |
probably damaging |
0.99 |
R0323:Spta1
|
UTSW |
1 |
174,046,017 (GRCm39) |
missense |
probably damaging |
1.00 |
R0508:Spta1
|
UTSW |
1 |
174,052,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R0698:Spta1
|
UTSW |
1 |
174,008,670 (GRCm39) |
missense |
probably damaging |
1.00 |
R0751:Spta1
|
UTSW |
1 |
174,012,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R0925:Spta1
|
UTSW |
1 |
174,001,992 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0941:Spta1
|
UTSW |
1 |
174,072,771 (GRCm39) |
unclassified |
probably benign |
|
R1131:Spta1
|
UTSW |
1 |
174,013,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R1171:Spta1
|
UTSW |
1 |
174,039,180 (GRCm39) |
nonsense |
probably null |
|
R1184:Spta1
|
UTSW |
1 |
174,012,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R1401:Spta1
|
UTSW |
1 |
174,050,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R1489:Spta1
|
UTSW |
1 |
174,058,891 (GRCm39) |
missense |
probably damaging |
0.97 |
R1532:Spta1
|
UTSW |
1 |
174,074,919 (GRCm39) |
missense |
probably damaging |
0.99 |
R1551:Spta1
|
UTSW |
1 |
174,067,732 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1555:Spta1
|
UTSW |
1 |
174,006,315 (GRCm39) |
missense |
probably damaging |
0.99 |
R1566:Spta1
|
UTSW |
1 |
174,012,272 (GRCm39) |
missense |
probably benign |
0.00 |
R1586:Spta1
|
UTSW |
1 |
174,041,061 (GRCm39) |
missense |
probably benign |
0.00 |
R1676:Spta1
|
UTSW |
1 |
174,007,405 (GRCm39) |
missense |
probably damaging |
0.98 |
R1711:Spta1
|
UTSW |
1 |
174,068,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R1795:Spta1
|
UTSW |
1 |
174,073,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R1823:Spta1
|
UTSW |
1 |
174,074,115 (GRCm39) |
missense |
probably benign |
0.05 |
R1842:Spta1
|
UTSW |
1 |
174,023,513 (GRCm39) |
missense |
probably benign |
0.00 |
R1867:Spta1
|
UTSW |
1 |
174,047,405 (GRCm39) |
missense |
probably benign |
0.33 |
R1970:Spta1
|
UTSW |
1 |
174,067,933 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2042:Spta1
|
UTSW |
1 |
174,039,213 (GRCm39) |
missense |
probably benign |
0.20 |
R2095:Spta1
|
UTSW |
1 |
174,071,764 (GRCm39) |
missense |
possibly damaging |
0.75 |
R2125:Spta1
|
UTSW |
1 |
174,035,910 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2145:Spta1
|
UTSW |
1 |
174,040,180 (GRCm39) |
missense |
probably benign |
0.00 |
R2158:Spta1
|
UTSW |
1 |
174,056,824 (GRCm39) |
missense |
probably benign |
0.41 |
R2187:Spta1
|
UTSW |
1 |
174,020,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R2250:Spta1
|
UTSW |
1 |
174,071,680 (GRCm39) |
missense |
probably damaging |
1.00 |
R2258:Spta1
|
UTSW |
1 |
174,001,907 (GRCm39) |
missense |
possibly damaging |
0.76 |
R2319:Spta1
|
UTSW |
1 |
174,006,222 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3782:Spta1
|
UTSW |
1 |
174,035,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R4058:Spta1
|
UTSW |
1 |
174,068,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R4080:Spta1
|
UTSW |
1 |
174,041,632 (GRCm39) |
missense |
probably benign |
0.00 |
R4081:Spta1
|
UTSW |
1 |
174,041,632 (GRCm39) |
missense |
probably benign |
0.00 |
R4082:Spta1
|
UTSW |
1 |
174,041,632 (GRCm39) |
missense |
probably benign |
0.00 |
R4108:Spta1
|
UTSW |
1 |
174,002,122 (GRCm39) |
missense |
probably benign |
0.01 |
R4115:Spta1
|
UTSW |
1 |
174,067,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R4303:Spta1
|
UTSW |
1 |
174,007,418 (GRCm39) |
missense |
probably damaging |
1.00 |
R4419:Spta1
|
UTSW |
1 |
174,074,990 (GRCm39) |
nonsense |
probably null |
|
R4525:Spta1
|
UTSW |
1 |
174,034,676 (GRCm39) |
missense |
probably null |
1.00 |
R4614:Spta1
|
UTSW |
1 |
174,020,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R4673:Spta1
|
UTSW |
1 |
174,018,628 (GRCm39) |
splice site |
probably null |
|
R4782:Spta1
|
UTSW |
1 |
174,058,232 (GRCm39) |
missense |
probably benign |
0.01 |
R4825:Spta1
|
UTSW |
1 |
174,071,608 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4829:Spta1
|
UTSW |
1 |
174,065,493 (GRCm39) |
missense |
probably benign |
0.01 |
R4873:Spta1
|
UTSW |
1 |
174,003,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R4875:Spta1
|
UTSW |
1 |
174,003,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R4898:Spta1
|
UTSW |
1 |
174,065,400 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4910:Spta1
|
UTSW |
1 |
174,045,429 (GRCm39) |
splice site |
probably null |
|
R4911:Spta1
|
UTSW |
1 |
174,013,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R4928:Spta1
|
UTSW |
1 |
174,018,622 (GRCm39) |
missense |
probably benign |
0.15 |
R4959:Spta1
|
UTSW |
1 |
174,074,174 (GRCm39) |
missense |
probably damaging |
0.97 |
R5009:Spta1
|
UTSW |
1 |
174,067,789 (GRCm39) |
missense |
possibly damaging |
0.62 |
R5149:Spta1
|
UTSW |
1 |
174,075,000 (GRCm39) |
missense |
probably damaging |
0.99 |
R5293:Spta1
|
UTSW |
1 |
174,023,551 (GRCm39) |
missense |
probably damaging |
0.99 |
R5421:Spta1
|
UTSW |
1 |
174,043,095 (GRCm39) |
missense |
probably damaging |
0.99 |
R5457:Spta1
|
UTSW |
1 |
174,044,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R5590:Spta1
|
UTSW |
1 |
174,003,336 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5606:Spta1
|
UTSW |
1 |
174,047,468 (GRCm39) |
missense |
probably damaging |
1.00 |
R5736:Spta1
|
UTSW |
1 |
174,041,821 (GRCm39) |
critical splice donor site |
probably null |
|
R5834:Spta1
|
UTSW |
1 |
174,012,363 (GRCm39) |
splice site |
probably null |
|
R5845:Spta1
|
UTSW |
1 |
174,068,662 (GRCm39) |
missense |
probably damaging |
0.97 |
R5987:Spta1
|
UTSW |
1 |
174,050,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R6102:Spta1
|
UTSW |
1 |
174,052,086 (GRCm39) |
missense |
probably benign |
0.01 |
R6221:Spta1
|
UTSW |
1 |
174,009,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R6276:Spta1
|
UTSW |
1 |
174,046,078 (GRCm39) |
missense |
probably damaging |
1.00 |
R6317:Spta1
|
UTSW |
1 |
174,068,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R6329:Spta1
|
UTSW |
1 |
174,041,743 (GRCm39) |
missense |
possibly damaging |
0.60 |
R6352:Spta1
|
UTSW |
1 |
174,039,212 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6374:Spta1
|
UTSW |
1 |
174,041,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R6376:Spta1
|
UTSW |
1 |
174,030,888 (GRCm39) |
missense |
probably benign |
|
R6387:Spta1
|
UTSW |
1 |
174,058,899 (GRCm39) |
missense |
probably benign |
0.01 |
R6451:Spta1
|
UTSW |
1 |
174,044,767 (GRCm39) |
missense |
probably damaging |
0.97 |
R6480:Spta1
|
UTSW |
1 |
174,014,714 (GRCm39) |
splice site |
probably null |
|
R6533:Spta1
|
UTSW |
1 |
174,071,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R6585:Spta1
|
UTSW |
1 |
174,006,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R6695:Spta1
|
UTSW |
1 |
174,071,608 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6945:Spta1
|
UTSW |
1 |
174,036,891 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7020:Spta1
|
UTSW |
1 |
174,036,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R7086:Spta1
|
UTSW |
1 |
174,027,050 (GRCm39) |
missense |
probably damaging |
0.98 |
R7087:Spta1
|
UTSW |
1 |
174,002,076 (GRCm39) |
missense |
probably benign |
|
R7151:Spta1
|
UTSW |
1 |
174,025,317 (GRCm39) |
missense |
probably damaging |
1.00 |
R7193:Spta1
|
UTSW |
1 |
174,012,178 (GRCm39) |
missense |
probably damaging |
1.00 |
R7199:Spta1
|
UTSW |
1 |
174,050,837 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7219:Spta1
|
UTSW |
1 |
174,050,203 (GRCm39) |
missense |
probably damaging |
0.96 |
R7343:Spta1
|
UTSW |
1 |
174,050,915 (GRCm39) |
missense |
probably damaging |
0.99 |
R7372:Spta1
|
UTSW |
1 |
174,025,201 (GRCm39) |
nonsense |
probably null |
|
R7472:Spta1
|
UTSW |
1 |
174,074,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R7516:Spta1
|
UTSW |
1 |
174,025,349 (GRCm39) |
missense |
probably damaging |
1.00 |
R7627:Spta1
|
UTSW |
1 |
174,032,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R7770:Spta1
|
UTSW |
1 |
174,023,547 (GRCm39) |
nonsense |
probably null |
|
R7784:Spta1
|
UTSW |
1 |
174,030,017 (GRCm39) |
missense |
probably damaging |
1.00 |
R7804:Spta1
|
UTSW |
1 |
174,023,471 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7854:Spta1
|
UTSW |
1 |
174,046,396 (GRCm39) |
critical splice donor site |
probably null |
|
R7862:Spta1
|
UTSW |
1 |
174,025,351 (GRCm39) |
critical splice donor site |
probably null |
|
R7958:Spta1
|
UTSW |
1 |
174,001,956 (GRCm39) |
missense |
probably benign |
0.03 |
R8015:Spta1
|
UTSW |
1 |
174,067,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R8059:Spta1
|
UTSW |
1 |
174,045,936 (GRCm39) |
intron |
probably benign |
|
R8076:Spta1
|
UTSW |
1 |
174,014,797 (GRCm39) |
missense |
probably benign |
0.00 |
R8152:Spta1
|
UTSW |
1 |
174,045,510 (GRCm39) |
missense |
probably benign |
0.03 |
R8235:Spta1
|
UTSW |
1 |
174,029,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R8284:Spta1
|
UTSW |
1 |
174,007,387 (GRCm39) |
missense |
probably benign |
0.00 |
R8298:Spta1
|
UTSW |
1 |
174,074,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R8312:Spta1
|
UTSW |
1 |
174,067,777 (GRCm39) |
missense |
probably damaging |
1.00 |
R8495:Spta1
|
UTSW |
1 |
174,043,051 (GRCm39) |
missense |
probably benign |
0.00 |
R8550:Spta1
|
UTSW |
1 |
174,014,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R8675:Spta1
|
UTSW |
1 |
174,058,249 (GRCm39) |
missense |
probably benign |
0.01 |
R8757:Spta1
|
UTSW |
1 |
174,040,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R8759:Spta1
|
UTSW |
1 |
174,040,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R8848:Spta1
|
UTSW |
1 |
174,025,310 (GRCm39) |
missense |
probably benign |
0.05 |
R8883:Spta1
|
UTSW |
1 |
174,021,145 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8884:Spta1
|
UTSW |
1 |
174,045,254 (GRCm39) |
critical splice donor site |
probably null |
|
R8896:Spta1
|
UTSW |
1 |
174,045,548 (GRCm39) |
missense |
probably damaging |
1.00 |
R8953:Spta1
|
UTSW |
1 |
174,058,241 (GRCm39) |
missense |
probably benign |
0.10 |
R9006:Spta1
|
UTSW |
1 |
174,047,537 (GRCm39) |
missense |
probably damaging |
1.00 |
R9013:Spta1
|
UTSW |
1 |
174,050,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R9077:Spta1
|
UTSW |
1 |
174,045,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R9129:Spta1
|
UTSW |
1 |
174,058,911 (GRCm39) |
missense |
possibly damaging |
0.77 |
R9207:Spta1
|
UTSW |
1 |
174,039,139 (GRCm39) |
missense |
probably benign |
0.01 |
R9229:Spta1
|
UTSW |
1 |
174,067,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R9281:Spta1
|
UTSW |
1 |
174,047,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R9290:Spta1
|
UTSW |
1 |
174,045,204 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9307:Spta1
|
UTSW |
1 |
174,035,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R9489:Spta1
|
UTSW |
1 |
174,035,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R9605:Spta1
|
UTSW |
1 |
174,035,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R9685:Spta1
|
UTSW |
1 |
174,032,925 (GRCm39) |
missense |
probably damaging |
1.00 |
RF002:Spta1
|
UTSW |
1 |
174,058,926 (GRCm39) |
missense |
possibly damaging |
0.62 |
RF018:Spta1
|
UTSW |
1 |
174,036,885 (GRCm39) |
missense |
probably damaging |
1.00 |
RF020:Spta1
|
UTSW |
1 |
174,045,469 (GRCm39) |
missense |
probably damaging |
1.00 |
RF020:Spta1
|
UTSW |
1 |
174,041,010 (GRCm39) |
missense |
probably benign |
0.42 |
T0722:Spta1
|
UTSW |
1 |
174,018,632 (GRCm39) |
splice site |
probably benign |
|
X0028:Spta1
|
UTSW |
1 |
174,052,016 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Spta1
|
UTSW |
1 |
174,067,933 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Spta1
|
UTSW |
1 |
174,018,617 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Spta1
|
UTSW |
1 |
174,073,255 (GRCm39) |
missense |
probably benign |
0.02 |
Z1177:Spta1
|
UTSW |
1 |
174,017,728 (GRCm39) |
missense |
probably benign |
0.09 |
|