Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9530002B09Rik |
C |
A |
4: 122,596,151 (GRCm39) |
Y127* |
probably null |
Het |
Adam33 |
C |
T |
2: 130,895,629 (GRCm39) |
G562D |
probably damaging |
Het |
Adh1 |
T |
C |
3: 137,988,557 (GRCm39) |
F177L |
probably damaging |
Het |
Arhgef17 |
T |
C |
7: 100,530,470 (GRCm39) |
T1439A |
probably damaging |
Het |
Arl5c |
C |
T |
11: 97,884,277 (GRCm39) |
E105K |
probably damaging |
Het |
Armc3 |
T |
A |
2: 19,293,740 (GRCm39) |
D510E |
possibly damaging |
Het |
Bbx |
T |
C |
16: 50,045,052 (GRCm39) |
E395G |
possibly damaging |
Het |
Cacna2d2 |
G |
A |
9: 107,404,364 (GRCm39) |
E1087K |
probably benign |
Het |
Casq1 |
T |
C |
1: 172,043,529 (GRCm39) |
N113S |
probably benign |
Het |
Cbfa2t3 |
A |
G |
8: 123,361,727 (GRCm39) |
S432P |
probably benign |
Het |
Ccn2 |
T |
C |
10: 24,472,377 (GRCm39) |
V140A |
probably benign |
Het |
Cd163 |
A |
G |
6: 124,294,781 (GRCm39) |
D615G |
probably damaging |
Het |
Chrnb2 |
A |
T |
3: 89,668,744 (GRCm39) |
D190E |
probably benign |
Het |
Clec9a |
T |
C |
6: 129,393,321 (GRCm39) |
L115P |
possibly damaging |
Het |
Cluh |
C |
T |
11: 74,552,550 (GRCm39) |
R532* |
probably null |
Het |
Cntnap5a |
T |
A |
1: 116,369,990 (GRCm39) |
L869Q |
probably damaging |
Het |
Cyp3a57 |
A |
T |
5: 145,305,944 (GRCm39) |
K143* |
probably null |
Het |
Dcaf12 |
G |
T |
4: 41,294,085 (GRCm39) |
H351N |
probably benign |
Het |
Dtna |
T |
A |
18: 23,702,805 (GRCm39) |
L112Q |
probably damaging |
Het |
Fnta |
G |
A |
8: 26,489,907 (GRCm39) |
Q303* |
probably null |
Het |
Frs2 |
T |
C |
10: 116,910,507 (GRCm39) |
E285G |
probably benign |
Het |
Gabra4 |
T |
C |
5: 71,781,455 (GRCm39) |
I293V |
probably damaging |
Het |
Gm2431 |
A |
T |
7: 141,811,518 (GRCm39) |
C129S |
unknown |
Het |
Gnl2 |
C |
T |
4: 124,928,111 (GRCm39) |
R49C |
probably damaging |
Het |
Helz |
T |
A |
11: 107,536,972 (GRCm39) |
Y275N |
probably damaging |
Het |
Hydin |
A |
G |
8: 111,189,289 (GRCm39) |
E1231G |
probably damaging |
Het |
Kctd11 |
T |
A |
11: 69,770,402 (GRCm39) |
D212V |
probably damaging |
Het |
Klf3 |
T |
A |
5: 64,979,245 (GRCm39) |
M29K |
probably benign |
Het |
Klhl21 |
T |
C |
4: 152,093,850 (GRCm39) |
S151P |
probably benign |
Het |
Lsm14b |
A |
T |
2: 179,673,580 (GRCm39) |
|
probably benign |
Het |
Mlxipl |
T |
C |
5: 135,150,974 (GRCm39) |
|
probably benign |
Het |
Mov10 |
G |
A |
3: 104,708,847 (GRCm39) |
R389C |
probably damaging |
Het |
Msh6 |
A |
G |
17: 88,295,661 (GRCm39) |
M1071V |
possibly damaging |
Het |
Myh8 |
G |
T |
11: 67,177,050 (GRCm39) |
A401S |
probably benign |
Het |
Ndufv3 |
T |
C |
17: 31,746,460 (GRCm39) |
S117P |
possibly damaging |
Het |
Obscn |
A |
T |
11: 58,984,410 (GRCm39) |
|
probably null |
Het |
Or1e22 |
T |
A |
11: 73,377,420 (GRCm39) |
T77S |
probably damaging |
Het |
Or2l13 |
T |
C |
16: 19,305,681 (GRCm39) |
I31T |
probably benign |
Het |
Or4c11c |
T |
C |
2: 88,661,634 (GRCm39) |
Y58H |
probably damaging |
Het |
Or8g50 |
T |
A |
9: 39,648,557 (GRCm39) |
Y149N |
probably damaging |
Het |
Pcdhb17 |
T |
A |
18: 37,619,375 (GRCm39) |
D388E |
probably benign |
Het |
Pgm3 |
T |
C |
9: 86,438,394 (GRCm39) |
T423A |
probably damaging |
Het |
Rufy4 |
T |
C |
1: 74,186,822 (GRCm39) |
C537R |
probably damaging |
Het |
S1pr5 |
T |
A |
9: 21,156,154 (GRCm39) |
T91S |
probably benign |
Het |
Sgcz |
T |
C |
8: 38,007,546 (GRCm39) |
|
probably benign |
Het |
Slc33a1 |
A |
G |
3: 63,871,376 (GRCm39) |
L79P |
probably damaging |
Het |
Slco2a1 |
A |
G |
9: 102,954,167 (GRCm39) |
T383A |
probably benign |
Het |
Slit1 |
G |
A |
19: 41,594,819 (GRCm39) |
R1184W |
probably damaging |
Het |
Stub1 |
A |
G |
17: 26,049,864 (GRCm39) |
Y304H |
probably damaging |
Het |
Taar7e |
T |
A |
10: 23,913,949 (GRCm39) |
Y146* |
probably null |
Het |
Tbc1d1 |
C |
T |
5: 64,473,844 (GRCm39) |
S660L |
probably benign |
Het |
Tcea2 |
C |
A |
2: 181,328,725 (GRCm39) |
F259L |
probably damaging |
Het |
Tcp11l1 |
T |
A |
2: 104,512,185 (GRCm39) |
K482N |
probably damaging |
Het |
Trpv6 |
C |
T |
6: 41,598,690 (GRCm39) |
R645Q |
probably damaging |
Het |
Uaca |
T |
A |
9: 60,748,125 (GRCm39) |
S30T |
probably benign |
Het |
Ubap2 |
C |
G |
4: 41,206,901 (GRCm39) |
V492L |
possibly damaging |
Het |
Ube3c |
T |
C |
5: 29,873,038 (GRCm39) |
F1026S |
probably damaging |
Het |
Vmn2r8 |
T |
G |
5: 108,956,487 (GRCm39) |
D45A |
possibly damaging |
Het |
Zfp738 |
G |
T |
13: 67,819,422 (GRCm39) |
L180I |
probably 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 |
R0454:Spta1
|
UTSW |
1 |
174,041,508 (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 |
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 |
|