Other mutations in this stock |
Total: 95 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
T |
C |
3: 137,774,780 (GRCm39) |
V1323A |
probably damaging |
Het |
Abcb1a |
T |
C |
5: 8,773,214 (GRCm39) |
L814P |
probably damaging |
Het |
Acat1 |
C |
A |
9: 53,502,756 (GRCm39) |
G191V |
probably damaging |
Het |
Acsbg3 |
A |
G |
17: 57,190,500 (GRCm39) |
|
probably null |
Het |
Adamts20 |
A |
T |
15: 94,224,277 (GRCm39) |
D1184E |
probably benign |
Het |
Adss1 |
T |
C |
12: 112,601,147 (GRCm39) |
L283P |
probably damaging |
Het |
Arid4a |
A |
G |
12: 71,070,272 (GRCm39) |
|
probably null |
Het |
Arid4b |
T |
A |
13: 14,359,023 (GRCm39) |
D599E |
probably benign |
Het |
AW146154 |
T |
C |
7: 41,130,057 (GRCm39) |
K353R |
possibly damaging |
Het |
Axdnd1 |
G |
T |
1: 156,204,216 (GRCm39) |
R547S |
possibly damaging |
Het |
Bcat1 |
A |
T |
6: 144,961,201 (GRCm39) |
F134Y |
probably damaging |
Het |
Camk2d |
C |
A |
3: 126,573,646 (GRCm39) |
|
probably benign |
Het |
Catsperg2 |
T |
G |
7: 29,400,550 (GRCm39) |
K268T |
probably damaging |
Het |
Ccar1 |
A |
C |
10: 62,581,114 (GRCm39) |
F1103L |
unknown |
Het |
Ccdc141 |
T |
A |
2: 76,905,260 (GRCm39) |
E395D |
probably damaging |
Het |
Cdc37l1 |
A |
G |
19: 28,967,983 (GRCm39) |
T16A |
probably benign |
Het |
Cdca2 |
T |
A |
14: 67,931,202 (GRCm39) |
|
probably null |
Het |
Cfap96 |
T |
C |
8: 46,420,952 (GRCm39) |
I159V |
probably damaging |
Het |
Cntn5 |
T |
G |
9: 9,976,288 (GRCm39) |
K219Q |
probably damaging |
Het |
Col23a1 |
C |
A |
11: 51,448,413 (GRCm39) |
A202E |
unknown |
Het |
Csmd1 |
G |
A |
8: 16,177,310 (GRCm39) |
L1318F |
probably damaging |
Het |
Csnk1g3 |
C |
T |
18: 54,028,895 (GRCm39) |
A16V |
possibly damaging |
Het |
Cspg4b |
A |
G |
13: 113,504,696 (GRCm39) |
I1942V |
probably benign |
Het |
Dab2 |
A |
G |
15: 6,454,162 (GRCm39) |
D224G |
probably damaging |
Het |
Ddr1 |
A |
T |
17: 35,996,005 (GRCm39) |
C625S |
probably damaging |
Het |
Dennd4a |
T |
C |
9: 64,796,338 (GRCm39) |
V788A |
probably damaging |
Het |
Dgcr2 |
T |
C |
16: 17,660,617 (GRCm39) |
E402G |
possibly damaging |
Het |
Dhcr7 |
T |
G |
7: 143,391,654 (GRCm39) |
I81S |
probably damaging |
Het |
Exd1 |
C |
T |
2: 119,350,807 (GRCm39) |
A485T |
probably benign |
Het |
Fat1 |
C |
T |
8: 45,489,199 (GRCm39) |
T3467I |
probably damaging |
Het |
Fblim1 |
T |
C |
4: 141,312,020 (GRCm39) |
E235G |
probably damaging |
Het |
Fbxo38 |
T |
A |
18: 62,651,662 (GRCm39) |
M548L |
probably benign |
Het |
Fstl5 |
T |
C |
3: 76,229,489 (GRCm39) |
Y97H |
probably damaging |
Het |
Glb1l |
A |
T |
1: 75,176,994 (GRCm39) |
S481T |
probably damaging |
Het |
Gp2 |
A |
T |
7: 119,056,407 (GRCm39) |
V22E |
possibly damaging |
Het |
Grin1 |
A |
G |
2: 25,208,736 (GRCm39) |
S55P |
possibly damaging |
Het |
Herc2 |
A |
G |
7: 55,756,240 (GRCm39) |
D760G |
probably benign |
Het |
Hpn |
A |
G |
7: 30,798,300 (GRCm39) |
|
probably benign |
Het |
Hsf2 |
T |
C |
10: 57,372,266 (GRCm39) |
V73A |
probably damaging |
Het |
Ighv1-42 |
T |
C |
12: 114,900,788 (GRCm39) |
Y80C |
probably benign |
Het |
Ighv1-64 |
T |
C |
12: 115,471,346 (GRCm39) |
K57R |
probably benign |
Het |
Klc1 |
T |
C |
12: 111,762,037 (GRCm39) |
I569T |
probably damaging |
Het |
Klra3 |
T |
G |
6: 130,300,579 (GRCm39) |
K263N |
probably benign |
Het |
Lrcol1 |
C |
A |
5: 110,502,393 (GRCm39) |
H90N |
probably benign |
Het |
Mamdc4 |
T |
C |
2: 25,455,368 (GRCm39) |
E921G |
possibly damaging |
Het |
Mark1 |
G |
A |
1: 184,637,724 (GRCm39) |
R622W |
possibly damaging |
Het |
Mdga1 |
A |
G |
17: 30,065,343 (GRCm39) |
S696P |
possibly damaging |
Het |
Mmp1b |
C |
T |
9: 7,370,729 (GRCm39) |
|
probably null |
Het |
Mplkipl1 |
C |
T |
19: 61,164,364 (GRCm39) |
G24R |
unknown |
Het |
Mtnr1a |
T |
C |
8: 45,538,652 (GRCm39) |
|
probably benign |
Het |
Myo5a |
T |
C |
9: 75,043,689 (GRCm39) |
I226T |
probably damaging |
Het |
Ncoa6 |
G |
T |
2: 155,257,147 (GRCm39) |
P799T |
probably damaging |
Het |
Npc1l1 |
C |
T |
11: 6,164,010 (GRCm39) |
|
probably null |
Het |
Nxph3 |
T |
C |
11: 95,402,321 (GRCm39) |
E31G |
probably benign |
Het |
Obscn |
T |
C |
11: 58,945,072 (GRCm39) |
I4649V |
probably null |
Het |
Or10d4b |
A |
T |
9: 39,534,734 (GRCm39) |
H103L |
probably damaging |
Het |
Or8b12b |
G |
T |
9: 37,684,243 (GRCm39) |
C96F |
probably damaging |
Het |
Or8g35 |
A |
T |
9: 39,381,663 (GRCm39) |
Y120N |
probably damaging |
Het |
Or8h10 |
G |
A |
2: 86,808,918 (GRCm39) |
S74L |
probably damaging |
Het |
P3h3 |
G |
A |
6: 124,818,601 (GRCm39) |
|
probably benign |
Het |
Pcnx2 |
A |
T |
8: 126,587,797 (GRCm39) |
|
probably null |
Het |
Pirb |
C |
T |
7: 3,720,602 (GRCm39) |
G299S |
probably benign |
Het |
Pla2g4d |
A |
G |
2: 120,097,224 (GRCm39) |
S792P |
probably damaging |
Het |
Plppr4 |
A |
T |
3: 117,129,240 (GRCm39) |
L76M |
possibly damaging |
Het |
Ppp2r3d |
A |
T |
9: 101,089,709 (GRCm39) |
S205T |
possibly damaging |
Het |
Prkdc |
G |
A |
16: 15,519,939 (GRCm39) |
D1126N |
possibly damaging |
Het |
Prrt4 |
G |
A |
6: 29,177,181 (GRCm39) |
S196L |
probably benign |
Het |
Ptpn21 |
A |
C |
12: 98,655,555 (GRCm39) |
S471A |
probably damaging |
Het |
Ptprk |
C |
A |
10: 28,456,480 (GRCm39) |
S9* |
probably null |
Het |
Rassf4 |
A |
T |
6: 116,622,103 (GRCm39) |
I163K |
possibly damaging |
Het |
Rgs22 |
C |
A |
15: 36,104,034 (GRCm39) |
R142S |
probably damaging |
Het |
Rit2 |
C |
A |
18: 31,345,726 (GRCm39) |
L73F |
probably damaging |
Het |
Rrbp1 |
A |
C |
2: 143,831,607 (GRCm39) |
S187A |
probably benign |
Het |
Rspo2 |
A |
T |
15: 42,956,583 (GRCm39) |
Y83* |
probably null |
Het |
Scn5a |
C |
T |
9: 119,363,773 (GRCm39) |
V456M |
probably benign |
Het |
Scn9a |
T |
A |
2: 66,382,057 (GRCm39) |
H290L |
probably benign |
Het |
Smarca4 |
T |
C |
9: 21,550,623 (GRCm39) |
I452T |
probably damaging |
Het |
Smc2 |
T |
A |
4: 52,449,612 (GRCm39) |
I198K |
probably damaging |
Het |
Smim14 |
G |
A |
5: 65,617,946 (GRCm39) |
|
probably benign |
Het |
Spg11 |
A |
C |
2: 121,938,936 (GRCm39) |
N339K |
probably benign |
Het |
Stk4 |
T |
C |
2: 163,941,747 (GRCm39) |
|
probably null |
Het |
Sypl1 |
C |
T |
12: 33,017,645 (GRCm39) |
T121M |
probably damaging |
Het |
Tas2r120 |
T |
A |
6: 132,634,331 (GRCm39) |
F138I |
probably benign |
Het |
Tcstv4 |
G |
A |
13: 120,769,926 (GRCm39) |
C82Y |
possibly damaging |
Het |
Tet2 |
A |
C |
3: 133,182,381 (GRCm39) |
C1194W |
possibly damaging |
Het |
Tex29 |
T |
C |
8: 11,905,668 (GRCm39) |
|
probably benign |
Het |
Tnfrsf22 |
T |
A |
7: 143,197,067 (GRCm39) |
T91S |
possibly damaging |
Het |
Tnik |
A |
T |
3: 28,593,690 (GRCm39) |
|
probably benign |
Het |
Tnr |
A |
T |
1: 159,685,974 (GRCm39) |
I402F |
probably benign |
Het |
Unc93b1 |
A |
T |
19: 3,994,293 (GRCm39) |
S475C |
probably damaging |
Het |
Utrn |
T |
A |
10: 12,539,205 (GRCm39) |
E1937D |
probably benign |
Het |
Vmn1r227 |
A |
T |
17: 20,955,927 (GRCm39) |
|
noncoding transcript |
Het |
Vmn2r101 |
G |
A |
17: 19,832,229 (GRCm39) |
V742I |
probably benign |
Het |
Vmn2r81 |
T |
C |
10: 79,083,635 (GRCm39) |
L3P |
possibly damaging |
Het |
Zfp882 |
T |
G |
8: 72,668,233 (GRCm39) |
H353Q |
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 |
|
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 |
|