Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb10 |
C |
T |
8: 124,688,791 (GRCm39) |
G495D |
probably damaging |
Het |
Apaf1 |
A |
G |
10: 90,894,268 (GRCm39) |
Y456H |
probably benign |
Het |
Arhgef11 |
A |
G |
3: 87,634,442 (GRCm39) |
N791S |
possibly damaging |
Het |
Brat1 |
A |
G |
5: 140,695,962 (GRCm39) |
Q66R |
possibly damaging |
Het |
Capn10 |
C |
T |
1: 92,874,668 (GRCm39) |
T633M |
probably damaging |
Het |
Ccdc186 |
G |
T |
19: 56,786,053 (GRCm39) |
L661I |
probably benign |
Het |
Cln3 |
A |
G |
7: 126,182,208 (GRCm39) |
S4P |
probably damaging |
Het |
Cnot10 |
G |
T |
9: 114,439,749 (GRCm39) |
S520Y |
probably damaging |
Het |
Csmd1 |
A |
T |
8: 16,129,978 (GRCm39) |
F1715I |
probably damaging |
Het |
Ezh2 |
A |
T |
6: 47,518,789 (GRCm39) |
C545* |
probably null |
Het |
Hivep1 |
C |
T |
13: 42,335,307 (GRCm39) |
S2282F |
probably damaging |
Het |
Jag2 |
T |
C |
12: 112,878,039 (GRCm39) |
E564G |
possibly damaging |
Het |
Kcnj16 |
A |
G |
11: 110,916,262 (GRCm39) |
H308R |
probably damaging |
Het |
Magi3 |
C |
T |
3: 103,935,126 (GRCm39) |
V936I |
probably benign |
Het |
Mcu |
G |
T |
10: 59,290,790 (GRCm39) |
A279E |
probably damaging |
Het |
Msln |
A |
G |
17: 25,973,157 (GRCm39) |
C13R |
probably damaging |
Het |
Nes |
A |
G |
3: 87,883,883 (GRCm39) |
D714G |
probably benign |
Het |
Nif3l1 |
T |
A |
1: 58,494,808 (GRCm39) |
V259D |
probably damaging |
Het |
Or4c127 |
A |
T |
2: 89,832,911 (GRCm39) |
M54L |
possibly damaging |
Het |
Or5k14 |
A |
C |
16: 58,693,206 (GRCm39) |
Y102* |
probably null |
Het |
Or8g18 |
G |
C |
9: 39,149,547 (GRCm39) |
P58A |
probably benign |
Het |
Pcdhb9 |
A |
G |
18: 37,536,169 (GRCm39) |
D721G |
possibly damaging |
Het |
Pepd |
A |
C |
7: 34,620,917 (GRCm39) |
T61P |
possibly damaging |
Het |
Pkd1l2 |
C |
T |
8: 117,746,282 (GRCm39) |
|
probably null |
Het |
Poglut3 |
A |
C |
9: 53,299,762 (GRCm39) |
R90S |
possibly damaging |
Het |
Psip1 |
A |
G |
4: 83,392,604 (GRCm39) |
S102P |
probably benign |
Het |
Ralgapa1 |
T |
C |
12: 55,809,446 (GRCm39) |
E443G |
possibly damaging |
Het |
Rnf20 |
A |
G |
4: 49,638,230 (GRCm39) |
D114G |
probably benign |
Het |
Schip1 |
A |
T |
3: 68,402,375 (GRCm39) |
I151F |
probably benign |
Het |
Smg1 |
T |
C |
7: 117,802,310 (GRCm39) |
T263A |
probably damaging |
Het |
Spn |
T |
C |
7: 126,735,445 (GRCm39) |
K354R |
possibly damaging |
Het |
Sspo |
G |
A |
6: 48,434,573 (GRCm39) |
A1022T |
probably damaging |
Het |
Strn |
A |
C |
17: 78,972,046 (GRCm39) |
|
probably null |
Het |
Tstd3 |
T |
C |
4: 21,759,627 (GRCm39) |
I79M |
probably damaging |
Het |
Txnl4a |
A |
G |
18: 80,250,487 (GRCm39) |
I28V |
probably benign |
Het |
Uty |
T |
C |
Y: 1,134,884 (GRCm39) |
D928G |
probably damaging |
Het |
Vps26c |
A |
G |
16: 94,313,225 (GRCm39) |
L22P |
probably damaging |
Het |
Vsx2 |
T |
A |
12: 84,623,085 (GRCm39) |
L163Q |
probably damaging |
Het |
|
Other mutations in Smarca2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01368:Smarca2
|
APN |
19 |
26,751,694 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01907:Smarca2
|
APN |
19 |
26,675,865 (GRCm39) |
missense |
possibly damaging |
0.59 |
IGL02039:Smarca2
|
APN |
19 |
26,693,537 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02110:Smarca2
|
APN |
19 |
26,650,140 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL02561:Smarca2
|
APN |
19 |
26,693,582 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02649:Smarca2
|
APN |
19 |
26,617,986 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL02880:Smarca2
|
APN |
19 |
26,654,024 (GRCm39) |
splice site |
probably benign |
|
IGL03028:Smarca2
|
APN |
19 |
26,655,712 (GRCm39) |
splice site |
probably benign |
|
IGL03187:Smarca2
|
APN |
19 |
26,650,224 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03213:Smarca2
|
APN |
19 |
26,601,375 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03354:Smarca2
|
APN |
19 |
26,597,303 (GRCm39) |
missense |
probably benign |
0.01 |
Genghis
|
UTSW |
19 |
26,597,284 (GRCm39) |
missense |
possibly damaging |
0.53 |
kraft
|
UTSW |
19 |
26,655,763 (GRCm39) |
missense |
probably damaging |
0.99 |
Kublai
|
UTSW |
19 |
26,618,013 (GRCm39) |
missense |
probably damaging |
1.00 |
Samarkand
|
UTSW |
19 |
26,631,864 (GRCm39) |
nonsense |
probably null |
|
tashkent
|
UTSW |
19 |
26,698,273 (GRCm39) |
missense |
probably benign |
0.06 |
Xanadu
|
UTSW |
19 |
26,659,452 (GRCm39) |
missense |
possibly damaging |
0.52 |
FR4737:Smarca2
|
UTSW |
19 |
26,608,399 (GRCm39) |
unclassified |
probably benign |
|
PIT1430001:Smarca2
|
UTSW |
19 |
26,626,493 (GRCm39) |
missense |
probably benign |
0.35 |
R0184:Smarca2
|
UTSW |
19 |
26,669,649 (GRCm39) |
nonsense |
probably null |
|
R0306:Smarca2
|
UTSW |
19 |
26,618,013 (GRCm39) |
missense |
probably damaging |
1.00 |
R0538:Smarca2
|
UTSW |
19 |
26,668,762 (GRCm39) |
missense |
probably damaging |
0.99 |
R0565:Smarca2
|
UTSW |
19 |
26,659,275 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0610:Smarca2
|
UTSW |
19 |
26,668,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R0669:Smarca2
|
UTSW |
19 |
26,683,600 (GRCm39) |
missense |
possibly damaging |
0.51 |
R0726:Smarca2
|
UTSW |
19 |
26,675,803 (GRCm39) |
missense |
probably damaging |
1.00 |
R1184:Smarca2
|
UTSW |
19 |
26,748,333 (GRCm39) |
splice site |
probably benign |
|
R1299:Smarca2
|
UTSW |
19 |
26,749,011 (GRCm39) |
critical splice donor site |
probably null |
|
R1306:Smarca2
|
UTSW |
19 |
26,748,388 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1381:Smarca2
|
UTSW |
19 |
26,608,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R1400:Smarca2
|
UTSW |
19 |
26,654,140 (GRCm39) |
missense |
probably damaging |
0.98 |
R1415:Smarca2
|
UTSW |
19 |
26,688,084 (GRCm39) |
missense |
probably null |
0.72 |
R1496:Smarca2
|
UTSW |
19 |
26,608,501 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1582:Smarca2
|
UTSW |
19 |
26,729,305 (GRCm39) |
missense |
probably damaging |
0.99 |
R1666:Smarca2
|
UTSW |
19 |
26,624,434 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1668:Smarca2
|
UTSW |
19 |
26,624,434 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1751:Smarca2
|
UTSW |
19 |
26,617,780 (GRCm39) |
splice site |
probably benign |
|
R1861:Smarca2
|
UTSW |
19 |
26,601,284 (GRCm39) |
missense |
probably benign |
0.03 |
R1962:Smarca2
|
UTSW |
19 |
26,650,124 (GRCm39) |
nonsense |
probably null |
|
R1964:Smarca2
|
UTSW |
19 |
26,650,124 (GRCm39) |
nonsense |
probably null |
|
R1998:Smarca2
|
UTSW |
19 |
26,608,493 (GRCm39) |
missense |
probably benign |
0.33 |
R2014:Smarca2
|
UTSW |
19 |
26,661,305 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2255:Smarca2
|
UTSW |
19 |
26,748,438 (GRCm39) |
missense |
probably benign |
0.01 |
R2392:Smarca2
|
UTSW |
19 |
26,618,050 (GRCm39) |
critical splice donor site |
probably null |
|
R2439:Smarca2
|
UTSW |
19 |
26,668,854 (GRCm39) |
critical splice donor site |
probably null |
|
R3030:Smarca2
|
UTSW |
19 |
26,729,429 (GRCm39) |
missense |
possibly damaging |
0.84 |
R3195:Smarca2
|
UTSW |
19 |
26,661,222 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3430:Smarca2
|
UTSW |
19 |
26,668,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R3710:Smarca2
|
UTSW |
19 |
26,646,290 (GRCm39) |
unclassified |
probably benign |
|
R3845:Smarca2
|
UTSW |
19 |
26,698,273 (GRCm39) |
missense |
probably benign |
0.06 |
R4013:Smarca2
|
UTSW |
19 |
26,661,327 (GRCm39) |
splice site |
probably null |
|
R4014:Smarca2
|
UTSW |
19 |
26,661,327 (GRCm39) |
splice site |
probably null |
|
R4016:Smarca2
|
UTSW |
19 |
26,661,327 (GRCm39) |
splice site |
probably null |
|
R4271:Smarca2
|
UTSW |
19 |
26,698,349 (GRCm39) |
critical splice donor site |
probably null |
|
R4471:Smarca2
|
UTSW |
19 |
26,597,277 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4612:Smarca2
|
UTSW |
19 |
26,753,625 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4730:Smarca2
|
UTSW |
19 |
26,608,073 (GRCm39) |
missense |
probably damaging |
1.00 |
R4755:Smarca2
|
UTSW |
19 |
26,631,883 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4999:Smarca2
|
UTSW |
19 |
26,698,255 (GRCm39) |
nonsense |
probably null |
|
R5015:Smarca2
|
UTSW |
19 |
26,668,788 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5320:Smarca2
|
UTSW |
19 |
26,668,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R5393:Smarca2
|
UTSW |
19 |
26,617,829 (GRCm39) |
missense |
probably benign |
0.18 |
R5503:Smarca2
|
UTSW |
19 |
26,659,446 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5503:Smarca2
|
UTSW |
19 |
26,601,336 (GRCm39) |
missense |
probably damaging |
0.96 |
R5715:Smarca2
|
UTSW |
19 |
26,626,522 (GRCm39) |
missense |
probably benign |
0.16 |
R5790:Smarca2
|
UTSW |
19 |
26,654,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R5874:Smarca2
|
UTSW |
19 |
26,753,469 (GRCm39) |
intron |
probably benign |
|
R6209:Smarca2
|
UTSW |
19 |
26,748,404 (GRCm39) |
nonsense |
probably null |
|
R6236:Smarca2
|
UTSW |
19 |
26,673,613 (GRCm39) |
missense |
probably benign |
0.33 |
R6291:Smarca2
|
UTSW |
19 |
26,608,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R6292:Smarca2
|
UTSW |
19 |
26,608,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R6325:Smarca2
|
UTSW |
19 |
26,655,763 (GRCm39) |
missense |
probably damaging |
0.99 |
R6544:Smarca2
|
UTSW |
19 |
26,608,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R6572:Smarca2
|
UTSW |
19 |
26,656,573 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6589:Smarca2
|
UTSW |
19 |
26,597,284 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6601:Smarca2
|
UTSW |
19 |
26,631,777 (GRCm39) |
missense |
probably benign |
0.30 |
R6804:Smarca2
|
UTSW |
19 |
26,729,286 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6922:Smarca2
|
UTSW |
19 |
26,668,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R7047:Smarca2
|
UTSW |
19 |
26,646,555 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7213:Smarca2
|
UTSW |
19 |
26,624,531 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7257:Smarca2
|
UTSW |
19 |
26,631,864 (GRCm39) |
nonsense |
probably null |
|
R7259:Smarca2
|
UTSW |
19 |
26,631,864 (GRCm39) |
nonsense |
probably null |
|
R7479:Smarca2
|
UTSW |
19 |
26,617,887 (GRCm39) |
missense |
probably benign |
0.00 |
R7512:Smarca2
|
UTSW |
19 |
26,661,209 (GRCm39) |
missense |
possibly damaging |
0.51 |
R8158:Smarca2
|
UTSW |
19 |
26,659,448 (GRCm39) |
missense |
probably benign |
0.16 |
R8182:Smarca2
|
UTSW |
19 |
26,608,120 (GRCm39) |
missense |
probably benign |
0.39 |
R8207:Smarca2
|
UTSW |
19 |
26,654,080 (GRCm39) |
missense |
possibly damaging |
0.71 |
R8467:Smarca2
|
UTSW |
19 |
26,597,121 (GRCm39) |
start codon destroyed |
probably null |
0.02 |
R8527:Smarca2
|
UTSW |
19 |
26,654,187 (GRCm39) |
missense |
probably damaging |
0.98 |
R8784:Smarca2
|
UTSW |
19 |
26,753,558 (GRCm39) |
missense |
probably benign |
0.17 |
R8898:Smarca2
|
UTSW |
19 |
26,608,358 (GRCm39) |
unclassified |
probably benign |
|
R9076:Smarca2
|
UTSW |
19 |
26,659,452 (GRCm39) |
missense |
possibly damaging |
0.52 |
R9123:Smarca2
|
UTSW |
19 |
26,693,583 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9125:Smarca2
|
UTSW |
19 |
26,693,583 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9317:Smarca2
|
UTSW |
19 |
26,737,279 (GRCm39) |
missense |
possibly damaging |
0.75 |
R9501:Smarca2
|
UTSW |
19 |
26,617,977 (GRCm39) |
missense |
probably benign |
0.04 |
R9514:Smarca2
|
UTSW |
19 |
26,659,452 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9641:Smarca2
|
UTSW |
19 |
26,656,498 (GRCm39) |
missense |
possibly damaging |
0.93 |
RF001:Smarca2
|
UTSW |
19 |
26,608,421 (GRCm39) |
unclassified |
probably benign |
|
RF001:Smarca2
|
UTSW |
19 |
26,608,386 (GRCm39) |
unclassified |
probably benign |
|
RF004:Smarca2
|
UTSW |
19 |
26,608,420 (GRCm39) |
unclassified |
probably benign |
|
RF019:Smarca2
|
UTSW |
19 |
26,608,401 (GRCm39) |
unclassified |
probably benign |
|
RF021:Smarca2
|
UTSW |
19 |
26,608,397 (GRCm39) |
unclassified |
probably benign |
|
RF024:Smarca2
|
UTSW |
19 |
26,608,420 (GRCm39) |
unclassified |
probably benign |
|
RF034:Smarca2
|
UTSW |
19 |
26,608,411 (GRCm39) |
unclassified |
probably benign |
|
RF040:Smarca2
|
UTSW |
19 |
26,608,422 (GRCm39) |
unclassified |
probably benign |
|
RF041:Smarca2
|
UTSW |
19 |
26,608,421 (GRCm39) |
unclassified |
probably benign |
|
RF047:Smarca2
|
UTSW |
19 |
26,608,405 (GRCm39) |
unclassified |
probably benign |
|
RF051:Smarca2
|
UTSW |
19 |
26,608,388 (GRCm39) |
unclassified |
probably benign |
|
X0061:Smarca2
|
UTSW |
19 |
26,698,240 (GRCm39) |
missense |
probably damaging |
0.98 |
|