Other mutations in this stock |
Total: 95 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca2 |
A |
T |
2: 25,334,868 (GRCm39) |
I1947F |
probably benign |
Het |
Adgrd1 |
G |
T |
5: 129,205,971 (GRCm39) |
V182F |
probably damaging |
Het |
Agmat |
A |
G |
4: 141,474,380 (GRCm39) |
D87G |
probably damaging |
Het |
AI182371 |
T |
C |
2: 34,978,749 (GRCm39) |
|
probably null |
Het |
Anapc1 |
G |
T |
2: 128,470,452 (GRCm39) |
H1559Q |
probably damaging |
Het |
Ankar |
T |
C |
1: 72,689,297 (GRCm39) |
Y1278C |
probably damaging |
Het |
Arhgef2 |
A |
T |
3: 88,546,628 (GRCm39) |
|
probably null |
Het |
Arsi |
G |
A |
18: 61,049,723 (GRCm39) |
G202E |
probably benign |
Het |
Banp |
A |
T |
8: 122,727,750 (GRCm39) |
I130F |
probably damaging |
Het |
C130050O18Rik |
G |
T |
5: 139,400,248 (GRCm39) |
R100S |
probably benign |
Het |
Carmil3 |
A |
G |
14: 55,733,739 (GRCm39) |
T374A |
possibly damaging |
Het |
Cc2d2a |
T |
A |
5: 43,879,812 (GRCm39) |
W1076R |
probably damaging |
Het |
Cdc34 |
T |
G |
10: 79,523,888 (GRCm39) |
S235A |
probably benign |
Het |
Cdh8 |
G |
T |
8: 99,757,656 (GRCm39) |
H647Q |
probably damaging |
Het |
Cdk1 |
A |
T |
10: 69,174,377 (GRCm39) |
L282Q |
probably damaging |
Het |
Ceacam3 |
A |
G |
7: 16,893,902 (GRCm39) |
D471G |
probably damaging |
Het |
Ciao2b |
A |
T |
8: 105,367,620 (GRCm39) |
I108N |
possibly damaging |
Het |
Cltc |
A |
T |
11: 86,648,105 (GRCm39) |
I4N |
probably benign |
Het |
Cntfr |
T |
A |
4: 41,658,816 (GRCm39) |
E305V |
probably damaging |
Het |
Cwh43 |
T |
A |
5: 73,591,653 (GRCm39) |
I496N |
probably damaging |
Het |
Cyp2f2 |
A |
G |
7: 26,829,149 (GRCm39) |
N218S |
probably benign |
Het |
D16Ertd472e |
A |
G |
16: 78,343,392 (GRCm39) |
|
probably null |
Het |
Dab2 |
A |
G |
15: 6,459,351 (GRCm39) |
Q400R |
possibly damaging |
Het |
Dapl1 |
A |
T |
2: 59,326,906 (GRCm39) |
I51F |
probably benign |
Het |
Drc7 |
G |
A |
8: 95,800,960 (GRCm39) |
|
probably null |
Het |
Etl4 |
A |
G |
2: 20,811,219 (GRCm39) |
T1101A |
probably damaging |
Het |
Fam83c |
C |
A |
2: 155,671,971 (GRCm39) |
R488M |
possibly damaging |
Het |
Fbxo42 |
A |
G |
4: 140,927,840 (GRCm39) |
T707A |
probably damaging |
Het |
Fcmr |
A |
T |
1: 130,803,922 (GRCm39) |
|
probably null |
Het |
Fer1l6 |
G |
C |
15: 58,518,930 (GRCm39) |
K1687N |
probably damaging |
Het |
Fgd4 |
G |
A |
16: 16,292,893 (GRCm39) |
R275* |
probably null |
Het |
Fxr2 |
G |
A |
11: 69,532,139 (GRCm39) |
C87Y |
possibly damaging |
Het |
Gja4 |
A |
T |
4: 127,206,472 (GRCm39) |
I97N |
probably damaging |
Het |
Gm136 |
A |
G |
4: 34,750,919 (GRCm39) |
|
probably null |
Het |
Gm14496 |
A |
G |
2: 181,642,837 (GRCm39) |
D836G |
possibly damaging |
Het |
Grm3 |
T |
A |
5: 9,561,520 (GRCm39) |
T777S |
probably damaging |
Het |
Guca2b |
A |
G |
4: 119,514,912 (GRCm39) |
Y50H |
probably damaging |
Het |
Herc2 |
C |
T |
7: 55,786,415 (GRCm39) |
P1587S |
probably benign |
Het |
Hmcn1 |
C |
T |
1: 150,545,309 (GRCm39) |
S2766N |
probably benign |
Het |
Idi2 |
T |
A |
13: 9,009,455 (GRCm39) |
I224K |
probably damaging |
Het |
Kmt2a |
A |
T |
9: 44,735,666 (GRCm39) |
|
probably benign |
Het |
Lonp2 |
A |
T |
8: 87,440,078 (GRCm39) |
M693L |
possibly damaging |
Het |
Megf8 |
G |
T |
7: 25,046,172 (GRCm39) |
M1525I |
possibly damaging |
Het |
Mgme1 |
T |
C |
2: 144,121,018 (GRCm39) |
V276A |
possibly damaging |
Het |
Mief2 |
G |
T |
11: 60,622,234 (GRCm39) |
W268L |
probably damaging |
Het |
Mpped1 |
C |
T |
15: 83,676,191 (GRCm39) |
|
probably benign |
Het |
Mreg |
T |
C |
1: 72,231,356 (GRCm39) |
N34S |
probably benign |
Het |
Myf6 |
T |
C |
10: 107,330,534 (GRCm39) |
Y11C |
probably damaging |
Het |
Myh9 |
C |
A |
15: 77,655,367 (GRCm39) |
Q1196H |
probably benign |
Het |
Myh9 |
A |
T |
15: 77,660,099 (GRCm39) |
D56E |
probably benign |
Het |
Myo5c |
A |
T |
9: 75,184,357 (GRCm39) |
R949S |
probably benign |
Het |
Ncapg2 |
TAA |
TA |
12: 116,398,305 (GRCm39) |
|
probably null |
Het |
Nfx1 |
T |
A |
4: 40,977,004 (GRCm39) |
V226E |
probably benign |
Het |
Nlrp10 |
T |
A |
7: 108,523,737 (GRCm39) |
K581M |
possibly damaging |
Het |
Nmd3 |
T |
G |
3: 69,647,317 (GRCm39) |
I273S |
probably benign |
Het |
Or4c3 |
A |
T |
2: 89,852,314 (GRCm39) |
I32N |
possibly damaging |
Het |
P4hb |
T |
C |
11: 120,462,442 (GRCm39) |
E88G |
probably damaging |
Het |
Pcnx3 |
A |
T |
19: 5,715,773 (GRCm39) |
H1444Q |
probably benign |
Het |
Pdia4 |
A |
T |
6: 47,776,133 (GRCm39) |
F421L |
possibly damaging |
Het |
Picalm |
T |
A |
7: 89,840,459 (GRCm39) |
S538T |
probably damaging |
Het |
Ppp2r2b |
T |
A |
18: 43,192,275 (GRCm39) |
I11F |
probably benign |
Het |
Prb1c |
A |
G |
6: 132,339,969 (GRCm39) |
|
probably null |
Het |
Ptk7 |
C |
T |
17: 46,884,460 (GRCm39) |
E757K |
possibly damaging |
Het |
Rbm22 |
T |
G |
18: 60,694,340 (GRCm39) |
C24W |
probably damaging |
Het |
Rev3l |
A |
G |
10: 39,682,658 (GRCm39) |
D288G |
probably damaging |
Het |
Rgs18 |
T |
A |
1: 144,629,791 (GRCm39) |
H156L |
probably benign |
Het |
Rnf213 |
A |
G |
11: 119,333,405 (GRCm39) |
I2871M |
probably damaging |
Het |
Rrm2b |
A |
T |
15: 37,945,328 (GRCm39) |
M137K |
probably damaging |
Het |
Rrp12 |
A |
T |
19: 41,857,224 (GRCm39) |
D1183E |
probably benign |
Het |
Sacs |
G |
A |
14: 61,441,277 (GRCm39) |
V1108M |
probably damaging |
Het |
Scube2 |
A |
T |
7: 109,442,421 (GRCm39) |
D270E |
possibly damaging |
Het |
Serpina3a |
T |
A |
12: 104,082,737 (GRCm39) |
F170Y |
probably damaging |
Het |
Serpinb3b |
T |
C |
1: 107,082,403 (GRCm39) |
E287G |
probably benign |
Het |
Slamf8 |
C |
T |
1: 172,412,186 (GRCm39) |
V130M |
probably damaging |
Het |
Slc5a3 |
T |
C |
16: 91,874,284 (GRCm39) |
S114P |
possibly damaging |
Het |
Sox10 |
A |
T |
15: 79,040,660 (GRCm39) |
D293E |
probably damaging |
Het |
Sphk1 |
A |
G |
11: 116,426,596 (GRCm39) |
D177G |
probably damaging |
Het |
Sphkap |
T |
G |
1: 83,256,121 (GRCm39) |
M543L |
probably benign |
Het |
Syt13 |
A |
T |
2: 92,783,760 (GRCm39) |
K343N |
probably damaging |
Het |
Tatdn3 |
A |
G |
1: 190,792,373 (GRCm39) |
M34T |
probably benign |
Het |
Timd4 |
T |
G |
11: 46,732,989 (GRCm39) |
V305G |
possibly damaging |
Het |
Tnnc2 |
T |
C |
2: 164,619,512 (GRCm39) |
I111V |
probably benign |
Het |
Togaram2 |
C |
T |
17: 72,004,846 (GRCm39) |
P301L |
probably benign |
Het |
Trpc3 |
T |
C |
3: 36,694,776 (GRCm39) |
N726S |
probably damaging |
Het |
Tspear |
T |
A |
10: 77,706,253 (GRCm39) |
L341H |
possibly damaging |
Het |
Ugt1a5 |
T |
A |
1: 88,093,805 (GRCm39) |
|
probably benign |
Het |
Ulk3 |
A |
T |
9: 57,500,443 (GRCm39) |
|
probably null |
Het |
Unc5d |
T |
A |
8: 29,250,777 (GRCm39) |
I297L |
probably benign |
Het |
Usp20 |
A |
G |
2: 30,908,830 (GRCm39) |
I804V |
probably benign |
Het |
Usp22 |
G |
T |
11: 61,052,144 (GRCm39) |
C278* |
probably null |
Het |
Usp53 |
A |
T |
3: 122,727,872 (GRCm39) |
N903K |
probably benign |
Het |
V1rd19 |
T |
C |
7: 23,702,812 (GRCm39) |
F93L |
probably benign |
Het |
Zdbf2 |
T |
A |
1: 63,343,493 (GRCm39) |
V624E |
possibly damaging |
Het |
Zfyve16 |
A |
T |
13: 92,645,528 (GRCm39) |
S1073T |
probably damaging |
Het |
Zkscan8 |
T |
C |
13: 21,710,765 (GRCm39) |
H115R |
possibly 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 |
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 |
R5566:Sos1
|
UTSW |
17 |
80,761,319 (GRCm39) |
missense |
possibly damaging |
0.91 |
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 |
|