Other mutations in this stock |
Total: 123 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl2fm3 |
T |
A |
3: 59,776,435 (GRCm39) |
|
probably null |
Het |
Adam3 |
T |
A |
8: 25,184,321 (GRCm39) |
I560L |
probably benign |
Het |
Agxt |
T |
C |
1: 93,063,436 (GRCm39) |
F113L |
probably benign |
Het |
Aknad1 |
T |
A |
3: 108,688,568 (GRCm39) |
|
probably null |
Het |
Alpk2 |
T |
A |
18: 65,399,357 (GRCm39) |
K2074* |
probably null |
Het |
Apob |
A |
G |
12: 8,057,848 (GRCm39) |
Y2077C |
probably damaging |
Het |
Arhgap17 |
A |
T |
7: 122,907,600 (GRCm39) |
L254Q |
probably damaging |
Het |
Arhgap26 |
T |
A |
18: 39,126,690 (GRCm39) |
|
probably benign |
Het |
Arhgef5 |
A |
G |
6: 43,249,762 (GRCm39) |
D171G |
probably benign |
Het |
Arid1b |
T |
A |
17: 5,392,478 (GRCm39) |
S2003T |
probably damaging |
Het |
Armc5 |
T |
G |
7: 127,839,900 (GRCm39) |
L406R |
possibly damaging |
Het |
Arsb |
T |
C |
13: 93,908,485 (GRCm39) |
V67A |
probably benign |
Het |
Aspm |
A |
G |
1: 139,419,281 (GRCm39) |
Y2982C |
probably damaging |
Het |
Bltp1 |
C |
A |
3: 37,052,348 (GRCm39) |
T3016K |
probably damaging |
Het |
Btbd7 |
A |
G |
12: 102,774,307 (GRCm39) |
L487P |
probably damaging |
Het |
Card11 |
C |
G |
5: 140,860,169 (GRCm39) |
D1063H |
probably damaging |
Het |
Ccdc186 |
G |
A |
19: 56,787,123 (GRCm39) |
T615M |
probably damaging |
Het |
Cd101 |
T |
A |
3: 100,901,205 (GRCm39) |
T960S |
probably benign |
Het |
Cdca7l |
C |
A |
12: 117,837,520 (GRCm39) |
S191* |
probably null |
Het |
Cemip |
A |
T |
7: 83,646,619 (GRCm39) |
I143N |
probably damaging |
Het |
Cep170 |
C |
T |
1: 176,609,829 (GRCm39) |
E161K |
possibly damaging |
Het |
Cfhr4 |
T |
G |
1: 139,702,301 (GRCm39) |
D61A |
probably damaging |
Het |
Chrm2 |
A |
T |
6: 36,501,168 (GRCm39) |
T342S |
probably benign |
Het |
Cib2 |
A |
G |
9: 54,457,163 (GRCm39) |
F34L |
probably benign |
Het |
Cnot1 |
A |
T |
8: 96,459,859 (GRCm39) |
I1836N |
probably benign |
Het |
Col4a3 |
C |
A |
1: 82,650,400 (GRCm39) |
P552Q |
unknown |
Het |
Cp |
T |
A |
3: 20,043,388 (GRCm39) |
|
probably benign |
Het |
Cul3 |
C |
T |
1: 80,267,806 (GRCm39) |
V112I |
probably benign |
Het |
Dcdc5 |
A |
G |
2: 106,195,895 (GRCm39) |
|
noncoding transcript |
Het |
Disp1 |
A |
T |
1: 182,917,027 (GRCm39) |
V133E |
probably damaging |
Het |
Dlg4 |
A |
G |
11: 69,921,751 (GRCm39) |
D30G |
probably damaging |
Het |
Dop1a |
C |
T |
9: 86,374,114 (GRCm39) |
T191I |
probably damaging |
Het |
Enam |
T |
G |
5: 88,650,173 (GRCm39) |
S561A |
probably benign |
Het |
Fbxw8 |
G |
T |
5: 118,263,092 (GRCm39) |
|
probably null |
Het |
Filip1 |
A |
G |
9: 79,725,214 (GRCm39) |
V1135A |
probably benign |
Het |
Galnt6 |
T |
C |
15: 100,614,059 (GRCm39) |
T81A |
probably benign |
Het |
Ghdc |
T |
C |
11: 100,657,814 (GRCm39) |
K472E |
probably benign |
Het |
Gm10568 |
T |
G |
1: 3,751,164 (GRCm39) |
|
noncoding transcript |
Het |
Gm4953 |
T |
A |
1: 158,995,929 (GRCm39) |
|
noncoding transcript |
Het |
Gm6871 |
T |
A |
7: 41,223,016 (GRCm39) |
H24L |
probably benign |
Het |
Gpr155 |
G |
A |
2: 73,197,882 (GRCm39) |
Q413* |
probably null |
Het |
Grhl2 |
A |
G |
15: 37,291,920 (GRCm39) |
|
probably null |
Het |
Ighv1-31 |
G |
C |
12: 114,793,128 (GRCm39) |
S36* |
probably null |
Het |
Ighv8-5 |
A |
G |
12: 115,031,462 (GRCm39) |
S26P |
probably damaging |
Het |
Igkv17-134 |
A |
C |
6: 67,697,910 (GRCm39) |
|
probably benign |
Het |
Igkv5-48 |
A |
C |
6: 69,703,833 (GRCm39) |
L24R |
probably damaging |
Het |
Isg20l2 |
T |
A |
3: 87,846,570 (GRCm39) |
V340E |
probably damaging |
Het |
Lrrtm1 |
A |
G |
6: 77,221,884 (GRCm39) |
Y447C |
probably damaging |
Het |
Ltbp1 |
T |
C |
17: 75,634,287 (GRCm39) |
S855P |
probably damaging |
Het |
Mgat4e |
A |
T |
1: 134,469,602 (GRCm39) |
N147K |
probably damaging |
Het |
Mlc1 |
A |
G |
15: 88,842,415 (GRCm39) |
L315P |
possibly damaging |
Het |
Mrgpra2a |
A |
G |
7: 47,076,292 (GRCm39) |
V322A |
probably benign |
Het |
Mroh7 |
T |
C |
4: 106,567,152 (GRCm39) |
|
probably null |
Het |
Mybpc1 |
T |
A |
10: 88,391,586 (GRCm39) |
K304* |
probably null |
Het |
Nlrp14 |
A |
C |
7: 106,785,790 (GRCm39) |
D622A |
possibly damaging |
Het |
Nlrp1b |
T |
A |
11: 71,108,103 (GRCm39) |
H466L |
probably benign |
Het |
Nlrp4d |
T |
A |
7: 10,112,336 (GRCm39) |
|
noncoding transcript |
Het |
Nrxn3 |
A |
G |
12: 89,227,130 (GRCm39) |
E628G |
possibly damaging |
Het |
Nup133 |
T |
C |
8: 124,653,870 (GRCm39) |
R530G |
possibly damaging |
Het |
Nup98 |
A |
G |
7: 101,845,007 (GRCm39) |
S21P |
unknown |
Het |
Or2h2b-ps1 |
T |
C |
17: 37,480,934 (GRCm39) |
I202V |
probably benign |
Het |
Or2l13b |
T |
C |
16: 19,348,768 (GRCm39) |
T301A |
probably benign |
Het |
Or4f14b |
A |
T |
2: 111,775,423 (GRCm39) |
I126K |
possibly damaging |
Het |
Or52e8 |
G |
A |
7: 104,624,686 (GRCm39) |
P169S |
possibly damaging |
Het |
Or5k1 |
T |
A |
16: 58,617,805 (GRCm39) |
T135S |
probably benign |
Het |
Or6c66 |
T |
C |
10: 129,461,676 (GRCm39) |
T85A |
probably damaging |
Het |
Or8c11 |
T |
A |
9: 38,290,038 (GRCm39) |
V287E |
probably null |
Het |
Otog |
A |
T |
7: 45,913,486 (GRCm39) |
Y773F |
probably damaging |
Het |
Otog |
A |
T |
7: 45,947,958 (GRCm39) |
I2320F |
probably damaging |
Het |
Otogl |
T |
C |
10: 107,715,378 (GRCm39) |
S433G |
probably benign |
Het |
Pcdhb17 |
A |
T |
18: 37,618,212 (GRCm39) |
M1L |
possibly damaging |
Het |
Pde7b |
T |
A |
10: 20,600,480 (GRCm39) |
|
probably benign |
Het |
Pgm1 |
T |
C |
4: 99,820,724 (GRCm39) |
V207A |
probably damaging |
Het |
Pkd1 |
T |
A |
17: 24,791,661 (GRCm39) |
V1116E |
probably damaging |
Het |
Pkd1l1 |
T |
A |
11: 8,879,360 (GRCm39) |
Y497F |
possibly damaging |
Het |
Pomgnt2 |
T |
C |
9: 121,812,013 (GRCm39) |
N256S |
probably benign |
Het |
Pot1a |
A |
T |
6: 25,746,020 (GRCm39) |
|
probably benign |
Het |
Prdm9 |
T |
C |
17: 15,764,585 (GRCm39) |
T732A |
probably benign |
Het |
Prg4 |
T |
A |
1: 150,331,574 (GRCm39) |
|
probably benign |
Het |
Ptpro |
T |
C |
6: 137,345,336 (GRCm39) |
V114A |
probably damaging |
Het |
Pyurf |
A |
G |
6: 57,668,933 (GRCm39) |
S20P |
unknown |
Het |
Rasgrf1 |
A |
G |
9: 89,858,805 (GRCm39) |
T488A |
probably benign |
Het |
Rassf8 |
A |
T |
6: 145,761,006 (GRCm39) |
K111* |
probably null |
Het |
Reps1 |
A |
T |
10: 17,983,436 (GRCm39) |
E426D |
probably damaging |
Het |
Robo2 |
T |
C |
16: 73,730,666 (GRCm39) |
K982R |
probably damaging |
Het |
Rps23 |
T |
C |
13: 91,071,871 (GRCm39) |
|
probably null |
Het |
Scamp4 |
T |
A |
10: 80,445,505 (GRCm39) |
V56E |
probably damaging |
Het |
Serpina1c |
C |
T |
12: 103,861,291 (GRCm39) |
V408I |
probably benign |
Het |
Sigirr |
A |
G |
7: 140,673,701 (GRCm39) |
W49R |
probably damaging |
Het |
Slc17a6 |
A |
T |
7: 51,308,489 (GRCm39) |
H271L |
possibly damaging |
Het |
Slc7a5 |
G |
T |
8: 122,611,861 (GRCm39) |
T389K |
probably damaging |
Het |
Slf1 |
T |
A |
13: 77,191,999 (GRCm39) |
H945L |
probably benign |
Het |
Slit3 |
T |
C |
11: 35,523,549 (GRCm39) |
S662P |
probably damaging |
Het |
Snta1 |
C |
A |
2: 154,218,938 (GRCm39) |
E466* |
probably null |
Het |
Sowaha |
A |
G |
11: 53,369,272 (GRCm39) |
L488P |
probably damaging |
Het |
Spata17 |
C |
A |
1: 186,926,208 (GRCm39) |
V41F |
probably damaging |
Het |
Srrm2 |
T |
A |
17: 24,034,362 (GRCm39) |
|
probably benign |
Het |
Stard13 |
T |
C |
5: 150,985,992 (GRCm39) |
N388S |
probably benign |
Het |
Stmn3 |
T |
C |
2: 180,950,630 (GRCm39) |
K59E |
probably damaging |
Het |
Sval1 |
A |
G |
6: 41,932,378 (GRCm39) |
N76S |
probably benign |
Het |
Svep1 |
T |
C |
4: 58,096,276 (GRCm39) |
H1448R |
possibly damaging |
Het |
Sycp2 |
A |
T |
2: 178,000,017 (GRCm39) |
D986E |
probably benign |
Het |
Sytl5 |
C |
T |
X: 9,781,841 (GRCm39) |
P181L |
possibly damaging |
Het |
Tbkbp1 |
G |
A |
11: 97,029,956 (GRCm39) |
S400L |
probably benign |
Het |
Tesc |
G |
T |
5: 118,194,531 (GRCm39) |
|
probably benign |
Het |
Tjp1 |
C |
T |
7: 64,993,475 (GRCm39) |
G33R |
probably damaging |
Het |
Tlr11 |
C |
A |
14: 50,600,346 (GRCm39) |
F777L |
probably benign |
Het |
Tmem156 |
A |
G |
5: 65,248,805 (GRCm39) |
|
probably benign |
Het |
Top3a |
A |
G |
11: 60,643,204 (GRCm39) |
|
probably benign |
Het |
Tpcn1 |
A |
G |
5: 120,694,584 (GRCm39) |
W162R |
probably damaging |
Het |
Tpd52l2 |
A |
T |
2: 181,157,005 (GRCm39) |
|
probably benign |
Het |
Trim80 |
G |
A |
11: 115,337,281 (GRCm39) |
G381D |
probably damaging |
Het |
Ugt1a10 |
C |
T |
1: 88,142,845 (GRCm39) |
P113L |
probably damaging |
Het |
Vmn2r117 |
TC |
T |
17: 23,698,487 (GRCm39) |
|
probably null |
Het |
Vmn2r56 |
T |
A |
7: 12,449,462 (GRCm39) |
I259F |
possibly damaging |
Het |
Vmn2r59 |
T |
C |
7: 41,693,077 (GRCm39) |
T508A |
probably benign |
Het |
Wdr73 |
A |
G |
7: 80,541,456 (GRCm39) |
V362A |
probably damaging |
Het |
Zdhhc21 |
G |
T |
4: 82,738,568 (GRCm39) |
T207K |
possibly damaging |
Het |
Zfp120 |
T |
A |
2: 149,959,872 (GRCm39) |
Q150L |
probably damaging |
Het |
Zfp212 |
C |
A |
6: 47,908,433 (GRCm39) |
Q471K |
possibly damaging |
Het |
Zfp804b |
C |
T |
5: 6,820,540 (GRCm39) |
G841D |
possibly damaging |
Het |
Znfx1 |
A |
T |
2: 166,878,724 (GRCm39) |
M1884K |
probably damaging |
Het |
Znfx1 |
G |
T |
2: 166,879,402 (GRCm39) |
A1658D |
probably benign |
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 |
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 |
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 |
|