Other mutations in this stock |
Total: 95 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700029H14Rik |
T |
C |
8: 13,612,237 (GRCm39) |
R38G |
possibly damaging |
Het |
4930590J08Rik |
T |
C |
6: 91,892,203 (GRCm39) |
V155A |
possibly damaging |
Het |
Adgb |
A |
G |
10: 10,302,349 (GRCm39) |
S406P |
probably damaging |
Het |
Adgrb2 |
C |
A |
4: 129,905,668 (GRCm39) |
T893N |
probably damaging |
Het |
Adgrf5 |
T |
C |
17: 43,735,484 (GRCm39) |
|
probably null |
Het |
Alms1 |
T |
A |
6: 85,605,487 (GRCm39) |
I2379N |
probably damaging |
Het |
Arap3 |
C |
T |
18: 38,122,965 (GRCm39) |
V512I |
probably benign |
Het |
Atf4 |
C |
T |
15: 80,141,414 (GRCm39) |
T268I |
probably benign |
Het |
Cblif |
G |
A |
19: 11,735,179 (GRCm39) |
M266I |
probably damaging |
Het |
Ccdc154 |
T |
C |
17: 25,382,156 (GRCm39) |
L25P |
probably damaging |
Het |
Ccdc9 |
G |
A |
7: 16,010,161 (GRCm39) |
S381F |
probably damaging |
Het |
Cdk17 |
C |
T |
10: 93,044,112 (GRCm39) |
T17M |
probably damaging |
Het |
Cep128 |
T |
C |
12: 91,314,352 (GRCm39) |
N142S |
probably benign |
Het |
Cep78 |
A |
G |
19: 15,936,900 (GRCm39) |
I602T |
probably damaging |
Het |
Clasp1 |
C |
T |
1: 118,475,755 (GRCm39) |
T935I |
probably damaging |
Het |
Cnr1 |
T |
C |
4: 33,945,000 (GRCm39) |
S463P |
probably damaging |
Het |
Cntnap1 |
T |
A |
11: 101,075,449 (GRCm39) |
W876R |
probably damaging |
Het |
Cntnap5c |
A |
G |
17: 58,349,545 (GRCm39) |
D286G |
probably damaging |
Het |
Copa |
C |
T |
1: 171,931,711 (GRCm39) |
R321C |
probably damaging |
Het |
Cspg4b |
A |
G |
13: 113,505,266 (GRCm39) |
T2132A |
possibly damaging |
Het |
Ctla2a |
T |
G |
13: 61,083,256 (GRCm39) |
E98A |
probably damaging |
Het |
Cux1 |
A |
T |
5: 136,421,176 (GRCm39) |
D183E |
probably damaging |
Het |
Cxcl15 |
A |
C |
5: 90,949,323 (GRCm39) |
T163P |
unknown |
Het |
Ddias |
T |
C |
7: 92,508,571 (GRCm39) |
N448S |
probably benign |
Het |
Dhx8 |
T |
C |
11: 101,657,564 (GRCm39) |
F1152S |
probably damaging |
Het |
Dnah12 |
C |
A |
14: 26,488,071 (GRCm39) |
Q992K |
probably benign |
Het |
Eno3 |
G |
T |
11: 70,552,251 (GRCm39) |
W301L |
possibly damaging |
Het |
Faap100 |
A |
T |
11: 120,268,059 (GRCm39) |
V238E |
probably damaging |
Het |
Fgf4 |
A |
G |
7: 144,416,049 (GRCm39) |
S137G |
probably benign |
Het |
Fhod3 |
A |
C |
18: 25,253,367 (GRCm39) |
D1439A |
possibly damaging |
Het |
Frem2 |
A |
G |
3: 53,560,778 (GRCm39) |
L1243P |
probably damaging |
Het |
Gkn3 |
T |
G |
6: 87,365,817 (GRCm39) |
M1L |
probably benign |
Het |
Gm10250 |
T |
C |
15: 5,150,509 (GRCm39) |
|
probably benign |
Het |
Gm12185 |
T |
C |
11: 48,798,859 (GRCm39) |
T545A |
possibly damaging |
Het |
Gm14226 |
T |
A |
2: 154,867,378 (GRCm39) |
L445H |
probably damaging |
Het |
Gm3404 |
A |
T |
5: 146,463,036 (GRCm39) |
M73L |
probably benign |
Het |
Gm973 |
G |
T |
1: 59,673,169 (GRCm39) |
R976S |
unknown |
Het |
Gpr146 |
A |
T |
5: 139,379,137 (GRCm39) |
H313L |
probably benign |
Het |
Gys2 |
T |
A |
6: 142,418,432 (GRCm39) |
E32D |
probably damaging |
Het |
Igsf9b |
A |
T |
9: 27,245,548 (GRCm39) |
T1172S |
possibly damaging |
Het |
Itga8 |
T |
A |
2: 12,270,144 (GRCm39) |
N114I |
possibly damaging |
Het |
Itsn2 |
T |
A |
12: 4,708,160 (GRCm39) |
V795E |
possibly damaging |
Het |
Kdm1b |
T |
A |
13: 47,214,244 (GRCm39) |
S197T |
probably benign |
Het |
Kif5c |
G |
A |
2: 49,613,145 (GRCm39) |
R161Q |
probably benign |
Het |
Krt33b |
T |
C |
11: 99,916,361 (GRCm39) |
Y232C |
probably damaging |
Het |
Lonrf2 |
G |
A |
1: 38,852,357 (GRCm39) |
P165S |
probably benign |
Het |
Lrp1 |
A |
T |
10: 127,424,453 (GRCm39) |
N744K |
possibly damaging |
Het |
Mcm10 |
C |
A |
2: 5,008,861 (GRCm39) |
L369F |
probably damaging |
Het |
Muc5ac |
T |
A |
7: 141,355,268 (GRCm39) |
I1018N |
possibly damaging |
Het |
Myom2 |
T |
C |
8: 15,115,795 (GRCm39) |
L70P |
probably benign |
Het |
Myt1l |
T |
A |
12: 29,877,241 (GRCm39) |
N297K |
unknown |
Het |
Ncr1 |
C |
T |
7: 4,343,807 (GRCm39) |
T98I |
probably benign |
Het |
Nek3 |
T |
C |
8: 22,650,278 (GRCm39) |
E78G |
probably damaging |
Het |
Nfatc3 |
T |
A |
8: 106,825,768 (GRCm39) |
N606K |
probably damaging |
Het |
Nup107 |
T |
G |
10: 117,597,248 (GRCm39) |
D669A |
probably damaging |
Het |
Or10ag52 |
A |
T |
2: 87,043,758 (GRCm39) |
Q174L |
probably benign |
Het |
Or10c1 |
A |
T |
17: 37,522,204 (GRCm39) |
I180N |
possibly damaging |
Het |
Or4c3 |
T |
C |
2: 89,851,673 (GRCm39) |
T246A |
probably benign |
Het |
Or8b55 |
A |
T |
9: 38,726,871 (GRCm39) |
H24L |
probably benign |
Het |
Pcnx1 |
T |
C |
12: 82,030,258 (GRCm39) |
V1711A |
probably benign |
Het |
Pik3c3 |
A |
G |
18: 30,410,063 (GRCm39) |
D99G |
probably damaging |
Het |
Pinx1 |
C |
A |
14: 64,157,024 (GRCm39) |
T317K |
probably benign |
Het |
Ppargc1b |
G |
T |
18: 61,431,857 (GRCm39) |
|
probably null |
Het |
Pradc1 |
T |
A |
6: 85,424,203 (GRCm39) |
I119F |
possibly damaging |
Het |
Psat1 |
G |
T |
19: 15,892,243 (GRCm39) |
T242K |
probably damaging |
Het |
Psma6 |
G |
A |
12: 55,454,317 (GRCm39) |
C28Y |
probably damaging |
Het |
Pyurf |
A |
T |
6: 57,668,817 (GRCm39) |
C58* |
probably null |
Het |
Rab3gap2 |
C |
A |
1: 185,016,081 (GRCm39) |
A1331E |
probably benign |
Het |
Rnase4 |
T |
C |
14: 51,342,722 (GRCm39) |
*149Q |
probably null |
Het |
Ruvbl2 |
T |
C |
7: 45,074,586 (GRCm39) |
K184R |
probably benign |
Het |
Scn7a |
T |
G |
2: 66,510,527 (GRCm39) |
M1292L |
probably benign |
Het |
Scn7a |
A |
T |
2: 66,531,231 (GRCm39) |
Y549N |
probably damaging |
Het |
Selp |
A |
G |
1: 163,959,854 (GRCm39) |
D370G |
possibly damaging |
Het |
Slc22a15 |
G |
A |
3: 101,767,769 (GRCm39) |
Q386* |
probably null |
Het |
Slc22a29 |
A |
G |
19: 8,195,126 (GRCm39) |
|
probably null |
Het |
Slc26a7 |
A |
C |
4: 14,548,491 (GRCm39) |
I266S |
possibly damaging |
Het |
Smpd4 |
T |
C |
16: 17,443,872 (GRCm39) |
S112P |
probably damaging |
Het |
Smpd4 |
T |
A |
16: 17,458,744 (GRCm39) |
L165Q |
probably damaging |
Het |
Snx33 |
A |
G |
9: 56,833,982 (GRCm39) |
I29T |
probably benign |
Het |
Spen |
G |
A |
4: 141,203,686 (GRCm39) |
P1647L |
unknown |
Het |
Strip2 |
T |
C |
6: 29,941,940 (GRCm39) |
|
probably null |
Het |
Swsap1 |
C |
T |
9: 21,867,280 (GRCm39) |
R75* |
probably null |
Het |
Tesl1 |
A |
G |
X: 23,772,990 (GRCm39) |
I164V |
probably benign |
Het |
Tmem210 |
C |
T |
2: 25,178,435 (GRCm39) |
T32I |
probably damaging |
Het |
Tnn |
C |
T |
1: 159,975,154 (GRCm39) |
R91H |
possibly damaging |
Het |
Tnni1 |
G |
A |
1: 135,736,420 (GRCm39) |
R94H |
probably damaging |
Het |
Tnrc6c |
T |
A |
11: 117,651,556 (GRCm39) |
V1693D |
probably benign |
Het |
Trip4 |
G |
A |
9: 65,782,259 (GRCm39) |
Q158* |
probably null |
Het |
Ttc39b |
T |
C |
4: 83,155,586 (GRCm39) |
E474G |
probably damaging |
Het |
Usp50 |
C |
A |
2: 126,617,782 (GRCm39) |
C221F |
probably damaging |
Het |
Vmn1r171 |
T |
C |
7: 23,331,781 (GRCm39) |
I2T |
probably benign |
Het |
Wdr62 |
T |
A |
7: 29,967,328 (GRCm39) |
I309F |
probably damaging |
Het |
Xdh |
A |
T |
17: 74,217,204 (GRCm39) |
V688E |
probably damaging |
Het |
Zfyve26 |
A |
G |
12: 79,285,718 (GRCm39) |
L2353P |
probably damaging |
Het |
Zgpat |
C |
A |
2: 181,020,633 (GRCm39) |
R269S |
probably damaging |
Het |
|
Other mutations in Igsf10 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00773:Igsf10
|
APN |
3 |
59,238,960 (GRCm39) |
missense |
probably benign |
0.03 |
IGL00790:Igsf10
|
APN |
3 |
59,226,938 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00916:Igsf10
|
APN |
3 |
59,238,548 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL00928:Igsf10
|
APN |
3 |
59,238,018 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01066:Igsf10
|
APN |
3 |
59,235,203 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01107:Igsf10
|
APN |
3 |
59,238,945 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01420:Igsf10
|
APN |
3 |
59,227,071 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01533:Igsf10
|
APN |
3 |
59,226,651 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01537:Igsf10
|
APN |
3 |
59,237,452 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01676:Igsf10
|
APN |
3 |
59,236,756 (GRCm39) |
missense |
probably benign |
0.17 |
IGL01676:Igsf10
|
APN |
3 |
59,233,432 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01960:Igsf10
|
APN |
3 |
59,226,158 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02123:Igsf10
|
APN |
3 |
59,226,081 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02198:Igsf10
|
APN |
3 |
59,233,399 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02268:Igsf10
|
APN |
3 |
59,238,573 (GRCm39) |
nonsense |
probably null |
|
IGL02313:Igsf10
|
APN |
3 |
59,238,111 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02368:Igsf10
|
APN |
3 |
59,235,652 (GRCm39) |
missense |
probably benign |
|
IGL02494:Igsf10
|
APN |
3 |
59,235,427 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02549:Igsf10
|
APN |
3 |
59,236,662 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02616:Igsf10
|
APN |
3 |
59,226,027 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02957:Igsf10
|
APN |
3 |
59,238,285 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03067:Igsf10
|
APN |
3 |
59,226,339 (GRCm39) |
missense |
probably benign |
0.25 |
IGL03104:Igsf10
|
APN |
3 |
59,226,905 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03124:Igsf10
|
APN |
3 |
59,227,086 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03212:Igsf10
|
APN |
3 |
59,235,586 (GRCm39) |
missense |
probably benign |
0.09 |
IGL03347:Igsf10
|
APN |
3 |
59,239,321 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03357:Igsf10
|
APN |
3 |
59,243,632 (GRCm39) |
missense |
probably benign |
0.35 |
F6893:Igsf10
|
UTSW |
3 |
59,238,481 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4449:Igsf10
|
UTSW |
3 |
59,226,531 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT1430001:Igsf10
|
UTSW |
3 |
59,235,579 (GRCm39) |
missense |
probably benign |
0.06 |
PIT4402001:Igsf10
|
UTSW |
3 |
59,233,000 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4810001:Igsf10
|
UTSW |
3 |
59,225,903 (GRCm39) |
missense |
probably damaging |
1.00 |
R0068:Igsf10
|
UTSW |
3 |
59,238,045 (GRCm39) |
missense |
probably damaging |
0.98 |
R0095:Igsf10
|
UTSW |
3 |
59,238,617 (GRCm39) |
nonsense |
probably null |
|
R0095:Igsf10
|
UTSW |
3 |
59,238,617 (GRCm39) |
nonsense |
probably null |
|
R0112:Igsf10
|
UTSW |
3 |
59,233,429 (GRCm39) |
missense |
probably benign |
0.00 |
R0141:Igsf10
|
UTSW |
3 |
59,238,253 (GRCm39) |
missense |
probably damaging |
1.00 |
R0538:Igsf10
|
UTSW |
3 |
59,227,527 (GRCm39) |
missense |
probably damaging |
0.99 |
R0551:Igsf10
|
UTSW |
3 |
59,236,089 (GRCm39) |
missense |
probably benign |
0.01 |
R0556:Igsf10
|
UTSW |
3 |
59,236,296 (GRCm39) |
missense |
probably benign |
0.02 |
R0582:Igsf10
|
UTSW |
3 |
59,227,188 (GRCm39) |
missense |
probably benign |
0.00 |
R0630:Igsf10
|
UTSW |
3 |
59,233,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R0675:Igsf10
|
UTSW |
3 |
59,236,015 (GRCm39) |
missense |
probably benign |
0.14 |
R0948:Igsf10
|
UTSW |
3 |
59,238,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R1252:Igsf10
|
UTSW |
3 |
59,239,269 (GRCm39) |
missense |
probably benign |
0.03 |
R1412:Igsf10
|
UTSW |
3 |
59,235,196 (GRCm39) |
splice site |
probably benign |
|
R1473:Igsf10
|
UTSW |
3 |
59,226,188 (GRCm39) |
missense |
probably damaging |
1.00 |
R1585:Igsf10
|
UTSW |
3 |
59,237,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R1650:Igsf10
|
UTSW |
3 |
59,233,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R1660:Igsf10
|
UTSW |
3 |
59,238,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R1671:Igsf10
|
UTSW |
3 |
59,235,921 (GRCm39) |
nonsense |
probably null |
|
R1748:Igsf10
|
UTSW |
3 |
59,226,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R1856:Igsf10
|
UTSW |
3 |
59,238,693 (GRCm39) |
missense |
possibly damaging |
0.63 |
R1912:Igsf10
|
UTSW |
3 |
59,236,993 (GRCm39) |
missense |
probably benign |
0.40 |
R2148:Igsf10
|
UTSW |
3 |
59,243,998 (GRCm39) |
missense |
possibly damaging |
0.77 |
R2155:Igsf10
|
UTSW |
3 |
59,239,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R2509:Igsf10
|
UTSW |
3 |
59,239,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R2511:Igsf10
|
UTSW |
3 |
59,239,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R2680:Igsf10
|
UTSW |
3 |
59,232,875 (GRCm39) |
missense |
probably benign |
0.14 |
R2913:Igsf10
|
UTSW |
3 |
59,239,157 (GRCm39) |
missense |
possibly damaging |
0.70 |
R2927:Igsf10
|
UTSW |
3 |
59,236,848 (GRCm39) |
missense |
probably benign |
|
R3547:Igsf10
|
UTSW |
3 |
59,243,935 (GRCm39) |
missense |
probably damaging |
1.00 |
R3547:Igsf10
|
UTSW |
3 |
59,237,962 (GRCm39) |
missense |
probably benign |
0.02 |
R3548:Igsf10
|
UTSW |
3 |
59,243,935 (GRCm39) |
missense |
probably damaging |
1.00 |
R3620:Igsf10
|
UTSW |
3 |
59,243,752 (GRCm39) |
missense |
probably damaging |
1.00 |
R3732:Igsf10
|
UTSW |
3 |
59,233,135 (GRCm39) |
missense |
probably benign |
0.29 |
R3743:Igsf10
|
UTSW |
3 |
59,233,546 (GRCm39) |
missense |
possibly damaging |
0.69 |
R3973:Igsf10
|
UTSW |
3 |
59,239,345 (GRCm39) |
missense |
probably damaging |
1.00 |
R4005:Igsf10
|
UTSW |
3 |
59,235,981 (GRCm39) |
missense |
probably benign |
0.00 |
R4184:Igsf10
|
UTSW |
3 |
59,227,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R4302:Igsf10
|
UTSW |
3 |
59,226,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R4404:Igsf10
|
UTSW |
3 |
59,236,972 (GRCm39) |
missense |
probably benign |
0.04 |
R4575:Igsf10
|
UTSW |
3 |
59,237,521 (GRCm39) |
missense |
probably benign |
|
R4676:Igsf10
|
UTSW |
3 |
59,233,370 (GRCm39) |
missense |
probably benign |
0.23 |
R4700:Igsf10
|
UTSW |
3 |
59,227,751 (GRCm39) |
missense |
probably damaging |
0.99 |
R4765:Igsf10
|
UTSW |
3 |
59,237,126 (GRCm39) |
missense |
probably benign |
0.01 |
R4986:Igsf10
|
UTSW |
3 |
59,236,027 (GRCm39) |
missense |
probably benign |
0.24 |
R5012:Igsf10
|
UTSW |
3 |
59,226,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R5070:Igsf10
|
UTSW |
3 |
59,235,714 (GRCm39) |
missense |
probably benign |
0.02 |
R5083:Igsf10
|
UTSW |
3 |
59,233,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R5336:Igsf10
|
UTSW |
3 |
59,227,553 (GRCm39) |
missense |
probably damaging |
1.00 |
R5462:Igsf10
|
UTSW |
3 |
59,233,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R5648:Igsf10
|
UTSW |
3 |
59,235,574 (GRCm39) |
missense |
probably benign |
0.01 |
R5810:Igsf10
|
UTSW |
3 |
59,226,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R5871:Igsf10
|
UTSW |
3 |
59,237,832 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5880:Igsf10
|
UTSW |
3 |
59,238,252 (GRCm39) |
missense |
probably damaging |
1.00 |
R5935:Igsf10
|
UTSW |
3 |
59,235,578 (GRCm39) |
missense |
probably benign |
0.12 |
R5979:Igsf10
|
UTSW |
3 |
59,243,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R6145:Igsf10
|
UTSW |
3 |
59,239,077 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6222:Igsf10
|
UTSW |
3 |
59,226,336 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6224:Igsf10
|
UTSW |
3 |
59,232,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R6264:Igsf10
|
UTSW |
3 |
59,235,928 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6283:Igsf10
|
UTSW |
3 |
59,226,870 (GRCm39) |
missense |
probably damaging |
1.00 |
R6336:Igsf10
|
UTSW |
3 |
59,237,760 (GRCm39) |
missense |
probably benign |
0.00 |
R6490:Igsf10
|
UTSW |
3 |
59,236,992 (GRCm39) |
missense |
probably benign |
0.06 |
R6785:Igsf10
|
UTSW |
3 |
59,226,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R6873:Igsf10
|
UTSW |
3 |
59,235,865 (GRCm39) |
missense |
probably benign |
|
R6889:Igsf10
|
UTSW |
3 |
59,239,354 (GRCm39) |
missense |
probably benign |
|
R7024:Igsf10
|
UTSW |
3 |
59,239,122 (GRCm39) |
missense |
probably benign |
0.00 |
R7056:Igsf10
|
UTSW |
3 |
59,238,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R7128:Igsf10
|
UTSW |
3 |
59,236,326 (GRCm39) |
missense |
probably benign |
|
R7251:Igsf10
|
UTSW |
3 |
59,226,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R7313:Igsf10
|
UTSW |
3 |
59,236,837 (GRCm39) |
missense |
probably benign |
0.05 |
R7340:Igsf10
|
UTSW |
3 |
59,233,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R7447:Igsf10
|
UTSW |
3 |
59,239,222 (GRCm39) |
missense |
probably benign |
0.39 |
R7506:Igsf10
|
UTSW |
3 |
59,226,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R7678:Igsf10
|
UTSW |
3 |
59,226,761 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7695:Igsf10
|
UTSW |
3 |
59,233,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R7709:Igsf10
|
UTSW |
3 |
59,238,964 (GRCm39) |
missense |
probably damaging |
0.96 |
R7749:Igsf10
|
UTSW |
3 |
59,236,549 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7808:Igsf10
|
UTSW |
3 |
59,235,489 (GRCm39) |
missense |
probably benign |
0.00 |
R7850:Igsf10
|
UTSW |
3 |
59,227,053 (GRCm39) |
missense |
probably benign |
0.33 |
R7879:Igsf10
|
UTSW |
3 |
59,238,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R7886:Igsf10
|
UTSW |
3 |
59,235,748 (GRCm39) |
missense |
probably benign |
0.01 |
R7891:Igsf10
|
UTSW |
3 |
59,235,832 (GRCm39) |
nonsense |
probably null |
|
R7946:Igsf10
|
UTSW |
3 |
59,227,125 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7948:Igsf10
|
UTSW |
3 |
59,239,279 (GRCm39) |
missense |
probably benign |
0.02 |
R8004:Igsf10
|
UTSW |
3 |
59,237,130 (GRCm39) |
missense |
probably benign |
0.01 |
R8096:Igsf10
|
UTSW |
3 |
59,236,380 (GRCm39) |
missense |
probably damaging |
0.98 |
R8141:Igsf10
|
UTSW |
3 |
59,237,949 (GRCm39) |
missense |
probably damaging |
0.96 |
R8183:Igsf10
|
UTSW |
3 |
59,238,036 (GRCm39) |
missense |
probably benign |
0.04 |
R8203:Igsf10
|
UTSW |
3 |
59,236,254 (GRCm39) |
missense |
probably benign |
0.11 |
R8325:Igsf10
|
UTSW |
3 |
59,225,954 (GRCm39) |
missense |
probably damaging |
0.96 |
R8350:Igsf10
|
UTSW |
3 |
59,238,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R8387:Igsf10
|
UTSW |
3 |
59,236,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R8488:Igsf10
|
UTSW |
3 |
59,227,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R8697:Igsf10
|
UTSW |
3 |
59,226,308 (GRCm39) |
missense |
probably benign |
0.02 |
R8786:Igsf10
|
UTSW |
3 |
59,238,063 (GRCm39) |
missense |
probably benign |
0.25 |
R8804:Igsf10
|
UTSW |
3 |
59,243,876 (GRCm39) |
missense |
probably damaging |
1.00 |
R8886:Igsf10
|
UTSW |
3 |
59,237,410 (GRCm39) |
missense |
probably benign |
0.00 |
R8902:Igsf10
|
UTSW |
3 |
59,243,633 (GRCm39) |
missense |
probably benign |
0.00 |
R8906:Igsf10
|
UTSW |
3 |
59,233,739 (GRCm39) |
missense |
probably benign |
0.01 |
R8917:Igsf10
|
UTSW |
3 |
59,226,888 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9051:Igsf10
|
UTSW |
3 |
59,236,668 (GRCm39) |
missense |
probably benign |
0.00 |
R9178:Igsf10
|
UTSW |
3 |
59,233,480 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9228:Igsf10
|
UTSW |
3 |
59,243,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R9230:Igsf10
|
UTSW |
3 |
59,243,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R9231:Igsf10
|
UTSW |
3 |
59,243,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R9232:Igsf10
|
UTSW |
3 |
59,243,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R9417:Igsf10
|
UTSW |
3 |
59,236,526 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9609:Igsf10
|
UTSW |
3 |
59,226,869 (GRCm39) |
missense |
probably damaging |
1.00 |
R9631:Igsf10
|
UTSW |
3 |
59,237,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R9689:Igsf10
|
UTSW |
3 |
59,233,624 (GRCm39) |
missense |
probably damaging |
1.00 |
R9762:Igsf10
|
UTSW |
3 |
59,237,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R9770:Igsf10
|
UTSW |
3 |
59,227,199 (GRCm39) |
missense |
probably benign |
0.07 |
R9798:Igsf10
|
UTSW |
3 |
59,239,126 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Igsf10
|
UTSW |
3 |
59,237,359 (GRCm39) |
missense |
possibly damaging |
0.59 |
Z1177:Igsf10
|
UTSW |
3 |
59,237,026 (GRCm39) |
nonsense |
probably null |
|
|