Other mutations in this stock |
Total: 97 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
T |
A |
11: 9,244,615 (GRCm39) |
Y2159* |
probably null |
Het |
Abca3 |
A |
G |
17: 24,602,901 (GRCm39) |
T499A |
probably benign |
Het |
Abcb5 |
T |
A |
12: 118,899,702 (GRCm39) |
T322S |
probably damaging |
Het |
Adamts4 |
T |
A |
1: 171,078,419 (GRCm39) |
M1K |
probably null |
Het |
Adamtsl4 |
C |
T |
3: 95,592,765 (GRCm39) |
|
probably null |
Het |
Adh4 |
A |
T |
3: 138,129,950 (GRCm39) |
I259F |
probably damaging |
Het |
Aff3 |
G |
A |
1: 38,220,505 (GRCm39) |
S1135F |
probably damaging |
Het |
Arhgef16 |
T |
C |
4: 154,370,105 (GRCm39) |
D280G |
probably benign |
Het |
Baiap3 |
T |
C |
17: 25,470,707 (GRCm39) |
E71G |
probably damaging |
Het |
Calb2 |
A |
G |
8: 110,879,332 (GRCm39) |
I91T |
possibly damaging |
Het |
Ccr5 |
A |
G |
9: 123,924,697 (GRCm39) |
N100S |
probably benign |
Het |
Cep57 |
G |
T |
9: 13,732,871 (GRCm39) |
R25S |
probably damaging |
Het |
Chadl |
A |
G |
15: 81,580,079 (GRCm39) |
L52P |
probably damaging |
Het |
Clec12b |
T |
C |
6: 129,362,438 (GRCm39) |
T6A |
probably damaging |
Het |
Cnga1 |
T |
A |
5: 72,775,593 (GRCm39) |
N43Y |
probably damaging |
Het |
Col20a1 |
A |
T |
2: 180,628,316 (GRCm39) |
|
probably null |
Het |
Csmd2 |
T |
C |
4: 128,356,682 (GRCm39) |
|
probably null |
Het |
Ctps1 |
A |
T |
4: 120,411,300 (GRCm39) |
|
probably null |
Het |
Cyp39a1 |
T |
A |
17: 43,996,099 (GRCm39) |
W224R |
possibly damaging |
Het |
Defb29 |
A |
T |
2: 152,380,848 (GRCm39) |
Y54N |
probably benign |
Het |
Dmbt1 |
A |
T |
7: 130,708,003 (GRCm39) |
D1241V |
probably damaging |
Het |
Dnah1 |
A |
T |
14: 30,996,323 (GRCm39) |
I2671K |
probably benign |
Het |
Dnah2 |
C |
A |
11: 69,407,395 (GRCm39) |
E158* |
probably null |
Het |
Dynlt2b |
A |
G |
16: 32,238,718 (GRCm39) |
Y31C |
probably damaging |
Het |
Edar |
A |
G |
10: 58,464,463 (GRCm39) |
S59P |
possibly damaging |
Het |
Egr2 |
T |
A |
10: 67,376,596 (GRCm39) |
C339* |
probably null |
Het |
Eif5b |
G |
A |
1: 38,084,765 (GRCm39) |
V871I |
possibly damaging |
Het |
Eif5b |
G |
A |
1: 38,090,328 (GRCm39) |
G1169E |
probably damaging |
Het |
Erap1 |
A |
G |
13: 74,810,531 (GRCm39) |
Y290C |
probably damaging |
Het |
Fastkd5 |
T |
A |
2: 130,456,221 (GRCm39) |
T790S |
possibly damaging |
Het |
Fkrp |
C |
T |
7: 16,544,849 (GRCm39) |
V338M |
probably damaging |
Het |
Gabra6 |
T |
C |
11: 42,198,317 (GRCm39) |
T378A |
probably benign |
Het |
Gm4924 |
C |
A |
10: 82,214,475 (GRCm39) |
Q17K |
possibly damaging |
Het |
Gm9847 |
A |
G |
12: 14,545,000 (GRCm39) |
|
noncoding transcript |
Het |
Gpr108 |
A |
G |
17: 57,543,919 (GRCm39) |
F429S |
probably damaging |
Het |
Gpr162 |
G |
A |
6: 124,837,901 (GRCm39) |
R250* |
probably null |
Het |
Gtf2a1 |
A |
T |
12: 91,534,368 (GRCm39) |
D295E |
possibly damaging |
Het |
Gtf2h3 |
C |
T |
5: 124,722,360 (GRCm39) |
T121I |
probably benign |
Het |
Herc1 |
T |
A |
9: 66,372,819 (GRCm39) |
M3125K |
possibly damaging |
Het |
Hoxb6 |
T |
A |
11: 96,191,580 (GRCm39) |
Y167* |
probably null |
Het |
Hrob |
T |
A |
11: 102,146,659 (GRCm39) |
S312T |
probably damaging |
Het |
Htt |
T |
C |
5: 35,006,419 (GRCm39) |
Y1443H |
probably damaging |
Het |
Il21r |
A |
G |
7: 125,224,470 (GRCm39) |
D28G |
probably damaging |
Het |
Impact |
T |
G |
18: 13,107,819 (GRCm39) |
V29G |
probably damaging |
Het |
Itpr3 |
A |
G |
17: 27,334,926 (GRCm39) |
T2147A |
possibly damaging |
Het |
Itsn2 |
T |
A |
12: 4,676,554 (GRCm39) |
L50Q |
probably damaging |
Het |
Jade1 |
A |
G |
3: 41,559,338 (GRCm39) |
D473G |
possibly damaging |
Het |
Kif26a |
T |
G |
12: 112,123,788 (GRCm39) |
L131R |
probably damaging |
Het |
Kif2a |
A |
T |
13: 107,130,432 (GRCm39) |
M1K |
probably null |
Het |
Lrsam1 |
C |
A |
2: 32,831,870 (GRCm39) |
Q368H |
probably damaging |
Het |
Macf1 |
T |
C |
4: 123,328,957 (GRCm39) |
Q4592R |
probably damaging |
Het |
Map3k5 |
T |
C |
10: 19,986,465 (GRCm39) |
V893A |
probably damaging |
Het |
Med13l |
G |
T |
5: 118,866,730 (GRCm39) |
V595F |
possibly damaging |
Het |
Mocs1 |
T |
A |
17: 49,761,211 (GRCm39) |
L435Q |
possibly damaging |
Het |
Mtmr4 |
T |
C |
11: 87,495,356 (GRCm39) |
L471P |
probably damaging |
Het |
Myo7a |
T |
C |
7: 97,714,023 (GRCm39) |
E1616G |
possibly damaging |
Het |
Nacad |
T |
A |
11: 6,552,136 (GRCm39) |
S352C |
probably damaging |
Het |
Nfat5 |
T |
A |
8: 108,095,767 (GRCm39) |
M817K |
possibly damaging |
Het |
Ofcc1 |
C |
A |
13: 40,248,129 (GRCm39) |
L668F |
probably damaging |
Het |
Or12j2 |
C |
A |
7: 139,915,980 (GRCm39) |
D68E |
probably damaging |
Het |
Or7e178 |
T |
C |
9: 20,225,265 (GRCm39) |
Q309R |
probably benign |
Het |
Or8j3c |
G |
A |
2: 86,253,721 (GRCm39) |
Q100* |
probably null |
Het |
Plxnb2 |
T |
C |
15: 89,048,223 (GRCm39) |
T696A |
probably benign |
Het |
Prkab2 |
T |
A |
3: 97,569,609 (GRCm39) |
F58L |
probably benign |
Het |
Prpf4 |
G |
T |
4: 62,334,206 (GRCm39) |
L220F |
probably benign |
Het |
Rad18 |
A |
T |
6: 112,658,307 (GRCm39) |
D199E |
probably benign |
Het |
Raet1e |
T |
C |
10: 22,050,304 (GRCm39) |
L29P |
probably damaging |
Het |
Ralgapb |
A |
C |
2: 158,336,630 (GRCm39) |
T1089P |
possibly damaging |
Het |
Rest |
A |
G |
5: 77,430,173 (GRCm39) |
E864G |
probably benign |
Het |
Rgsl1 |
T |
A |
1: 153,669,520 (GRCm39) |
I289F |
probably damaging |
Het |
Rint1 |
T |
C |
5: 24,015,951 (GRCm39) |
Y406H |
probably damaging |
Het |
Rmc1 |
T |
C |
18: 12,313,749 (GRCm39) |
I26T |
possibly damaging |
Het |
Rpl31 |
C |
T |
1: 39,409,108 (GRCm39) |
R41C |
probably benign |
Het |
Scn8a |
T |
C |
15: 100,872,415 (GRCm39) |
S485P |
probably damaging |
Het |
Slamf1 |
T |
A |
1: 171,615,538 (GRCm39) |
V249E |
possibly damaging |
Het |
Slc39a12 |
C |
T |
2: 14,412,414 (GRCm39) |
T362I |
possibly damaging |
Het |
Srcap |
T |
C |
7: 127,124,475 (GRCm39) |
F215S |
probably damaging |
Het |
Supt4a |
T |
A |
11: 87,634,113 (GRCm39) |
S110T |
probably benign |
Het |
Tbc1d30 |
T |
A |
10: 121,138,015 (GRCm39) |
T232S |
probably damaging |
Het |
Tenm3 |
A |
G |
8: 48,732,041 (GRCm39) |
C1288R |
probably damaging |
Het |
Tespa1 |
T |
A |
10: 130,191,356 (GRCm39) |
L100* |
probably null |
Het |
Tgm1 |
C |
A |
14: 55,949,893 (GRCm39) |
R105L |
probably damaging |
Het |
Tgoln1 |
G |
A |
6: 72,593,018 (GRCm39) |
T154I |
possibly damaging |
Het |
Trp53i13 |
G |
A |
11: 77,399,552 (GRCm39) |
T259I |
probably damaging |
Het |
Tubgcp4 |
T |
A |
2: 121,015,251 (GRCm39) |
F320I |
possibly damaging |
Het |
Tut7 |
A |
T |
13: 59,936,443 (GRCm39) |
C817* |
probably null |
Het |
Vmn1r21 |
A |
C |
6: 57,821,079 (GRCm39) |
Y122D |
probably benign |
Het |
Vmn1r75 |
T |
A |
7: 11,614,407 (GRCm39) |
D46E |
probably damaging |
Het |
Vmn2r120 |
A |
T |
17: 57,852,290 (GRCm39) |
L9M |
possibly damaging |
Het |
Vmn2r59 |
A |
G |
7: 41,696,247 (GRCm39) |
I165T |
possibly damaging |
Het |
Vmn2r76 |
A |
T |
7: 85,875,286 (GRCm39) |
Y564N |
probably damaging |
Het |
Wee1 |
G |
T |
7: 109,725,257 (GRCm39) |
E300* |
probably null |
Het |
Xdh |
T |
C |
17: 74,200,617 (GRCm39) |
D1168G |
probably damaging |
Het |
Zfp54 |
A |
G |
17: 21,653,706 (GRCm39) |
T67A |
probably damaging |
Het |
Zfp941 |
G |
T |
7: 140,392,679 (GRCm39) |
H227N |
probably benign |
Het |
Zpr1 |
T |
A |
9: 46,192,373 (GRCm39) |
V399D |
possibly damaging |
Het |
Zzz3 |
A |
G |
3: 152,161,461 (GRCm39) |
E285G |
probably damaging |
Het |
|
Other mutations in Sos1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00805:Sos1
|
APN |
17 |
80,705,953 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL00915:Sos1
|
APN |
17 |
80,741,367 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00929:Sos1
|
APN |
17 |
80,716,025 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01073:Sos1
|
APN |
17 |
80,730,176 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01116:Sos1
|
APN |
17 |
80,752,929 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01533:Sos1
|
APN |
17 |
80,722,511 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01546:Sos1
|
APN |
17 |
80,716,040 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01583:Sos1
|
APN |
17 |
80,741,329 (GRCm39) |
missense |
probably benign |
0.11 |
IGL01628:Sos1
|
APN |
17 |
80,730,106 (GRCm39) |
splice site |
probably benign |
|
IGL01837:Sos1
|
APN |
17 |
80,730,157 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02170:Sos1
|
APN |
17 |
80,705,719 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02426:Sos1
|
APN |
17 |
80,742,372 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02992:Sos1
|
APN |
17 |
80,726,445 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03037:Sos1
|
APN |
17 |
80,727,758 (GRCm39) |
missense |
probably damaging |
0.98 |
1mM(1):Sos1
|
UTSW |
17 |
80,762,486 (GRCm39) |
missense |
possibly damaging |
0.46 |
BB007:Sos1
|
UTSW |
17 |
80,714,267 (GRCm39) |
missense |
probably benign |
0.00 |
BB017:Sos1
|
UTSW |
17 |
80,714,267 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4354001:Sos1
|
UTSW |
17 |
80,756,785 (GRCm39) |
missense |
possibly damaging |
0.52 |
R0056:Sos1
|
UTSW |
17 |
80,721,050 (GRCm39) |
missense |
probably damaging |
1.00 |
R0348:Sos1
|
UTSW |
17 |
80,715,740 (GRCm39) |
missense |
probably benign |
|
R0373:Sos1
|
UTSW |
17 |
80,761,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R0477:Sos1
|
UTSW |
17 |
80,742,363 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0621:Sos1
|
UTSW |
17 |
80,759,408 (GRCm39) |
critical splice donor site |
probably null |
|
R0839:Sos1
|
UTSW |
17 |
80,741,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R1174:Sos1
|
UTSW |
17 |
80,753,037 (GRCm39) |
nonsense |
probably null |
|
R1490:Sos1
|
UTSW |
17 |
80,721,104 (GRCm39) |
missense |
probably benign |
0.11 |
R1566:Sos1
|
UTSW |
17 |
80,761,345 (GRCm39) |
missense |
probably damaging |
0.99 |
R1635:Sos1
|
UTSW |
17 |
80,730,108 (GRCm39) |
splice site |
probably null |
|
R3412:Sos1
|
UTSW |
17 |
80,714,146 (GRCm39) |
missense |
probably benign |
|
R3770:Sos1
|
UTSW |
17 |
80,705,737 (GRCm39) |
missense |
probably damaging |
0.97 |
R3951:Sos1
|
UTSW |
17 |
80,731,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R3964:Sos1
|
UTSW |
17 |
80,762,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R3966:Sos1
|
UTSW |
17 |
80,762,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R4086:Sos1
|
UTSW |
17 |
80,756,781 (GRCm39) |
missense |
probably benign |
0.06 |
R4087:Sos1
|
UTSW |
17 |
80,756,781 (GRCm39) |
missense |
probably benign |
0.06 |
R4089:Sos1
|
UTSW |
17 |
80,756,781 (GRCm39) |
missense |
probably benign |
0.06 |
R4194:Sos1
|
UTSW |
17 |
80,706,013 (GRCm39) |
missense |
probably benign |
0.02 |
R4468:Sos1
|
UTSW |
17 |
80,761,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R4469:Sos1
|
UTSW |
17 |
80,761,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R4597:Sos1
|
UTSW |
17 |
80,741,255 (GRCm39) |
missense |
probably benign |
0.05 |
R4773:Sos1
|
UTSW |
17 |
80,705,660 (GRCm39) |
missense |
probably damaging |
0.99 |
R4923:Sos1
|
UTSW |
17 |
80,742,381 (GRCm39) |
missense |
probably benign |
0.10 |
R5120:Sos1
|
UTSW |
17 |
80,715,677 (GRCm39) |
missense |
probably damaging |
0.98 |
R5478:Sos1
|
UTSW |
17 |
80,741,276 (GRCm39) |
missense |
probably damaging |
1.00 |
R5984:Sos1
|
UTSW |
17 |
80,759,561 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6053:Sos1
|
UTSW |
17 |
80,722,463 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6153:Sos1
|
UTSW |
17 |
80,756,764 (GRCm39) |
missense |
probably benign |
0.01 |
R6567:Sos1
|
UTSW |
17 |
80,740,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R7392:Sos1
|
UTSW |
17 |
80,731,629 (GRCm39) |
missense |
probably damaging |
1.00 |
R7623:Sos1
|
UTSW |
17 |
80,787,323 (GRCm39) |
missense |
probably benign |
0.28 |
R7763:Sos1
|
UTSW |
17 |
80,721,142 (GRCm39) |
missense |
probably benign |
|
R7930:Sos1
|
UTSW |
17 |
80,714,267 (GRCm39) |
missense |
probably benign |
0.00 |
R8132:Sos1
|
UTSW |
17 |
80,716,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R8236:Sos1
|
UTSW |
17 |
80,715,712 (GRCm39) |
missense |
probably benign |
0.41 |
R8322:Sos1
|
UTSW |
17 |
80,715,728 (GRCm39) |
missense |
probably damaging |
0.96 |
R8348:Sos1
|
UTSW |
17 |
80,741,548 (GRCm39) |
missense |
probably benign |
0.00 |
R8448:Sos1
|
UTSW |
17 |
80,741,548 (GRCm39) |
missense |
probably benign |
0.00 |
R8554:Sos1
|
UTSW |
17 |
80,705,842 (GRCm39) |
missense |
probably damaging |
0.99 |
R8850:Sos1
|
UTSW |
17 |
80,741,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R8966:Sos1
|
UTSW |
17 |
80,705,879 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9051:Sos1
|
UTSW |
17 |
80,715,723 (GRCm39) |
missense |
probably benign |
|
R9355:Sos1
|
UTSW |
17 |
80,722,479 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9378:Sos1
|
UTSW |
17 |
80,761,239 (GRCm39) |
missense |
probably damaging |
1.00 |
R9576:Sos1
|
UTSW |
17 |
80,742,367 (GRCm39) |
missense |
probably benign |
0.11 |
X0020:Sos1
|
UTSW |
17 |
80,756,706 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Sos1
|
UTSW |
17 |
80,761,347 (GRCm39) |
missense |
probably benign |
0.05 |
|