Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca12 |
A |
C |
1: 71,297,257 (GRCm39) |
L2411R |
probably damaging |
Het |
Als2 |
A |
G |
1: 59,245,746 (GRCm39) |
W577R |
probably damaging |
Het |
Aox1 |
C |
A |
1: 58,346,518 (GRCm39) |
R551S |
probably benign |
Het |
Areg |
A |
T |
5: 91,294,577 (GRCm39) |
H245L |
possibly damaging |
Het |
Arhgap35 |
T |
C |
7: 16,297,392 (GRCm39) |
T558A |
possibly damaging |
Het |
Arhgef28 |
A |
T |
13: 98,073,368 (GRCm39) |
C1322* |
probably null |
Het |
Arhgef38 |
T |
C |
3: 132,912,719 (GRCm39) |
R107G |
possibly damaging |
Het |
Atf7ip |
T |
A |
6: 136,548,500 (GRCm39) |
F695L |
probably damaging |
Het |
AW209491 |
C |
T |
13: 14,812,365 (GRCm39) |
A406V |
probably benign |
Het |
Bche |
T |
G |
3: 73,556,011 (GRCm39) |
Q549P |
possibly damaging |
Het |
Blnk |
A |
G |
19: 40,917,733 (GRCm39) |
F417L |
possibly damaging |
Het |
Bloc1s1 |
T |
G |
10: 128,759,255 (GRCm39) |
K17T |
probably damaging |
Het |
C330018D20Rik |
G |
T |
18: 57,090,968 (GRCm39) |
T65K |
probably damaging |
Het |
Ccdc168 |
A |
T |
1: 44,096,417 (GRCm39) |
N1560K |
probably benign |
Het |
Cers1 |
T |
A |
8: 70,774,228 (GRCm39) |
S162T |
possibly damaging |
Het |
Cgn |
T |
C |
3: 94,686,832 (GRCm39) |
K157E |
probably benign |
Het |
Cldn7 |
G |
A |
11: 69,858,494 (GRCm39) |
R196Q |
probably benign |
Het |
Clrn2 |
C |
A |
5: 45,611,369 (GRCm39) |
Q73K |
probably benign |
Het |
Cmss1 |
A |
G |
16: 57,122,608 (GRCm39) |
V262A |
probably benign |
Het |
Cpb2 |
T |
A |
14: 75,498,128 (GRCm39) |
V97E |
probably damaging |
Het |
Ctnnd2 |
G |
A |
15: 30,683,387 (GRCm39) |
V463I |
probably benign |
Het |
Cyp7a1 |
A |
T |
4: 6,268,476 (GRCm39) |
S416R |
probably benign |
Het |
Dip2b |
C |
T |
15: 100,087,960 (GRCm39) |
R965C |
probably damaging |
Het |
Dkk3 |
T |
C |
7: 111,749,865 (GRCm39) |
T102A |
probably benign |
Het |
Dmap1 |
C |
A |
4: 117,538,039 (GRCm39) |
|
probably null |
Het |
Dnah12 |
C |
A |
14: 26,608,828 (GRCm39) |
D3872E |
possibly damaging |
Het |
Dnah7b |
A |
G |
1: 46,158,558 (GRCm39) |
|
probably null |
Het |
Dnai1 |
C |
T |
4: 41,632,391 (GRCm39) |
T575I |
probably benign |
Het |
Dsg1a |
T |
A |
18: 20,464,599 (GRCm39) |
Y365N |
probably damaging |
Het |
Dusp11 |
T |
A |
6: 85,936,215 (GRCm39) |
K18* |
probably null |
Het |
E2f2 |
A |
T |
4: 135,900,245 (GRCm39) |
T52S |
probably benign |
Het |
Elavl4 |
A |
G |
4: 110,147,841 (GRCm39) |
L13S |
probably benign |
Het |
Epor |
T |
C |
9: 21,873,572 (GRCm39) |
D59G |
possibly damaging |
Het |
Eral1 |
A |
G |
11: 77,971,059 (GRCm39) |
C43R |
possibly damaging |
Het |
Fam135b |
A |
G |
15: 71,362,697 (GRCm39) |
V228A |
probably benign |
Het |
Gba1 |
T |
C |
3: 89,113,129 (GRCm39) |
S187P |
probably damaging |
Het |
Gcc2 |
G |
T |
10: 58,091,669 (GRCm39) |
|
probably benign |
Het |
Gdap2 |
C |
A |
3: 100,109,572 (GRCm39) |
|
probably benign |
Het |
Gm10271 |
A |
T |
10: 116,808,497 (GRCm39) |
F6L |
probably damaging |
Het |
Gm10801 |
C |
CGTG |
2: 98,494,152 (GRCm39) |
|
probably null |
Het |
Gpr160 |
T |
C |
3: 30,950,612 (GRCm39) |
L228P |
probably benign |
Het |
Gsdmc2 |
A |
C |
15: 63,702,715 (GRCm39) |
V184G |
probably benign |
Het |
Gtf2e2 |
A |
T |
8: 34,266,080 (GRCm39) |
K252M |
probably damaging |
Het |
Gtf2e2 |
G |
T |
8: 34,266,081 (GRCm39) |
K252N |
probably benign |
Het |
Gys1 |
T |
C |
7: 45,087,529 (GRCm39) |
Y102H |
probably benign |
Het |
H4c2 |
A |
G |
13: 23,941,209 (GRCm39) |
D69G |
probably damaging |
Het |
Ifit3b |
A |
C |
19: 34,589,598 (GRCm39) |
D258A |
probably damaging |
Het |
Itpr3 |
T |
A |
17: 27,323,575 (GRCm39) |
M1200K |
probably damaging |
Het |
Kcng4 |
A |
T |
8: 120,353,098 (GRCm39) |
F271I |
probably damaging |
Het |
Klhdc2 |
C |
T |
12: 69,350,387 (GRCm39) |
S144L |
possibly damaging |
Het |
Lhcgr |
A |
G |
17: 89,063,006 (GRCm39) |
F222S |
probably damaging |
Het |
Lrp5 |
C |
G |
19: 3,678,299 (GRCm39) |
G519R |
probably damaging |
Het |
Magel2 |
T |
C |
7: 62,028,515 (GRCm39) |
V473A |
probably benign |
Het |
Map1a |
T |
C |
2: 121,134,776 (GRCm39) |
V1864A |
possibly damaging |
Het |
Mast4 |
T |
A |
13: 102,895,242 (GRCm39) |
Q760H |
probably damaging |
Het |
Mertk |
A |
G |
2: 128,613,294 (GRCm39) |
N437D |
probably benign |
Het |
Mettl18 |
G |
A |
1: 163,824,344 (GRCm39) |
V222I |
probably benign |
Het |
Mical2 |
C |
T |
7: 111,934,155 (GRCm39) |
T782M |
probably benign |
Het |
Mocos |
T |
A |
18: 24,819,750 (GRCm39) |
V664E |
probably damaging |
Het |
Neb |
G |
T |
2: 52,185,306 (GRCm39) |
N975K |
probably benign |
Het |
Nectin3 |
A |
T |
16: 46,284,508 (GRCm39) |
S59T |
probably benign |
Het |
Nelfb |
A |
T |
2: 25,093,900 (GRCm39) |
M11K |
probably damaging |
Het |
Nrp1 |
A |
G |
8: 129,202,650 (GRCm39) |
N545S |
probably damaging |
Het |
Or10ak11 |
T |
C |
4: 118,687,478 (GRCm39) |
D53G |
probably damaging |
Het |
Or2g1 |
T |
A |
17: 38,107,248 (GRCm39) |
N304K |
probably benign |
Het |
Or51b4 |
T |
A |
7: 103,530,907 (GRCm39) |
D181V |
probably damaging |
Het |
Or5b117 |
A |
T |
19: 13,431,324 (GRCm39) |
S186T |
possibly damaging |
Het |
Or5p67 |
T |
A |
7: 107,922,254 (GRCm39) |
T210S |
probably benign |
Het |
Or6c70 |
A |
T |
10: 129,710,390 (GRCm39) |
F79I |
probably damaging |
Het |
Or8g53 |
T |
C |
9: 39,683,836 (GRCm39) |
T87A |
probably benign |
Het |
P3h1 |
A |
G |
4: 119,103,862 (GRCm39) |
H587R |
probably damaging |
Het |
Paqr4 |
A |
G |
17: 23,958,832 (GRCm39) |
|
probably null |
Het |
Pde12 |
A |
G |
14: 26,390,253 (GRCm39) |
V152A |
probably benign |
Het |
Ppip5k1 |
C |
A |
2: 121,180,972 (GRCm39) |
E45* |
probably null |
Het |
Ptch2 |
C |
T |
4: 116,967,254 (GRCm39) |
A677V |
probably benign |
Het |
Rgs12 |
A |
G |
5: 35,177,689 (GRCm39) |
N93S |
probably damaging |
Het |
Rif1 |
C |
G |
2: 51,985,856 (GRCm39) |
L614V |
probably damaging |
Het |
Rnf32 |
T |
C |
5: 29,408,145 (GRCm39) |
S125P |
probably damaging |
Het |
Robo4 |
A |
G |
9: 37,322,696 (GRCm39) |
I850V |
probably damaging |
Het |
Scap |
T |
A |
9: 110,210,219 (GRCm39) |
I876N |
probably damaging |
Het |
Sin3a |
A |
G |
9: 57,034,484 (GRCm39) |
D1219G |
possibly damaging |
Het |
Skint5 |
T |
C |
4: 113,743,005 (GRCm39) |
E354G |
unknown |
Het |
Spart |
A |
G |
3: 55,033,962 (GRCm39) |
D396G |
probably benign |
Het |
Spindoc |
G |
A |
19: 7,351,024 (GRCm39) |
S311L |
probably benign |
Het |
Tbck |
T |
C |
3: 132,507,278 (GRCm39) |
I750T |
possibly damaging |
Het |
Tmem191 |
T |
C |
16: 17,094,334 (GRCm39) |
|
probably null |
Het |
Trgv1 |
A |
T |
13: 19,524,474 (GRCm39) |
Y66F |
probably benign |
Het |
Vmn2r125 |
A |
G |
4: 156,702,292 (GRCm39) |
Y26C |
probably damaging |
Het |
Zbtb17 |
T |
C |
4: 141,192,128 (GRCm39) |
C358R |
possibly damaging |
Het |
Zfp180 |
G |
A |
7: 23,804,859 (GRCm39) |
G426E |
probably damaging |
Het |
Zfp445 |
A |
G |
9: 122,682,951 (GRCm39) |
V330A |
probably benign |
Het |
Zfp595 |
A |
G |
13: 67,465,688 (GRCm39) |
C192R |
probably damaging |
Het |
Zkscan4 |
A |
G |
13: 21,668,623 (GRCm39) |
H387R |
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 |
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 |
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 |
|