Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A030005L19Rik |
G |
GTGGCTGCTA |
1: 82,891,311 (GRCm39) |
|
probably benign |
Het |
Acer1 |
A |
G |
17: 57,265,909 (GRCm39) |
V122A |
probably benign |
Het |
Adam34l |
T |
G |
8: 44,079,942 (GRCm39) |
D94A |
possibly damaging |
Het |
Ankhd1 |
GGCGGC |
GGCGGCAGCGGC |
18: 36,693,974 (GRCm39) |
|
probably benign |
Het |
Ankrd24 |
C |
CGGAGGCAGAGGA |
10: 81,479,405 (GRCm39) |
|
probably benign |
Het |
Atp13a1 |
C |
A |
8: 70,252,720 (GRCm39) |
A680D |
probably damaging |
Het |
Blm |
CGCCTCCTCCTC |
CGCCTCCTCCTCAGCCTCCTCCTC |
7: 80,162,651 (GRCm39) |
|
probably benign |
Het |
Blm |
CTCCTCC |
CTCCTCCTCCTCGTCCTCC |
7: 80,162,675 (GRCm39) |
|
probably benign |
Het |
Blm |
CTCCTCCTCCTCCTCCTCCTCCTC |
CTCCTCCTCCTCATCCTCCTCCTCCTCCTCCTCCTC |
7: 80,162,654 (GRCm39) |
|
probably benign |
Het |
Cad |
GT |
G |
5: 31,217,556 (GRCm39) |
|
probably benign |
Het |
Calhm1 |
GC |
GCTGTGGCTGTGTC |
19: 47,129,715 (GRCm39) |
|
probably benign |
Het |
Casz1 |
CACA |
C |
4: 149,036,761 (GRCm39) |
|
probably benign |
Het |
Cherp |
GACCTGGA |
G |
8: 73,215,893 (GRCm39) |
|
probably null |
Het |
Chga |
AGC |
AGCTGC |
12: 102,527,682 (GRCm39) |
|
probably benign |
Het |
Coq7 |
A |
G |
7: 118,132,405 (GRCm39) |
S24P |
probably benign |
Het |
Cul1 |
T |
C |
6: 47,501,515 (GRCm39) |
V734A |
possibly damaging |
Het |
Cyb5r4 |
GCCCAGGGATGTGACAGACACACT |
GCCCAGGGATGTGACAGACACACTCCCCAGGGATGTGACAGACACACT |
9: 86,922,469 (GRCm39) |
|
probably benign |
Het |
Dgkz |
A |
T |
2: 91,770,286 (GRCm39) |
F521I |
possibly damaging |
Het |
Fam171b |
GCAGCA |
GCAGCATCAGCA |
2: 83,643,230 (GRCm39) |
|
probably benign |
Het |
Fat1 |
T |
G |
8: 45,442,003 (GRCm39) |
S1102A |
probably benign |
Het |
Gab3 |
CTT |
CTTTTT |
X: 74,043,624 (GRCm39) |
|
probably benign |
Het |
Gm14412 |
T |
C |
2: 177,008,894 (GRCm39) |
I52V |
probably benign |
Het |
Gm5414 |
T |
C |
15: 101,536,388 (GRCm39) |
E79G |
probably benign |
Het |
Gpc5 |
G |
A |
14: 115,654,590 (GRCm39) |
S470N |
probably benign |
Het |
Grin2b |
A |
G |
6: 136,021,238 (GRCm39) |
V21A |
probably benign |
Het |
Hecw1 |
C |
A |
13: 14,472,009 (GRCm39) |
C553F |
probably damaging |
Het |
Hsd3b6 |
T |
A |
3: 98,713,756 (GRCm39) |
H181L |
probably benign |
Het |
Il2 |
CCAGGTGCTGCTGC |
CC |
3: 37,179,911 (GRCm39) |
|
probably benign |
Het |
Inpp5f |
G |
A |
7: 128,296,807 (GRCm39) |
G1053R |
probably damaging |
Het |
Kcnma1 |
T |
G |
14: 23,361,765 (GRCm39) |
Y1142S |
probably damaging |
Het |
Kctd8 |
T |
C |
5: 69,267,775 (GRCm39) |
K445R |
possibly damaging |
Het |
Kmt2b |
CC |
CCTCCTTC |
7: 30,285,807 (GRCm39) |
|
probably benign |
Het |
Kmt2c |
TG |
TGTTGCGG |
5: 25,520,773 (GRCm39) |
|
probably benign |
Het |
Krtap28-10 |
CACCAC |
CACCACCGCCACCGCAACCAC |
1: 83,020,003 (GRCm39) |
|
probably benign |
Het |
Krtap28-10 |
CACAGCCACAGCCACCACAGCCACAGCCAC |
CACAGCCACAGCCACAACAGCCACAGCCACCACAGCCACAGCCAC |
1: 83,019,976 (GRCm39) |
|
probably benign |
Het |
Krtap28-10 |
GCCACCACAGC |
GCCACCACAGCCACATCCACCACAGC |
1: 83,020,001 (GRCm39) |
|
probably benign |
Het |
Lama1 |
A |
G |
17: 68,059,897 (GRCm39) |
D662G |
|
Het |
Lce1m |
AC |
ACTGCTGCTGCCCC |
3: 92,925,459 (GRCm39) |
|
probably benign |
Het |
Lce1m |
GCTGCCACC |
GCTGCCACCACTCCTGCCACC |
3: 92,925,576 (GRCm39) |
|
probably benign |
Het |
Lmo4 |
A |
C |
3: 143,907,623 (GRCm39) |
S63A |
possibly damaging |
Het |
Lrrk2 |
T |
C |
15: 91,620,836 (GRCm39) |
I952T |
probably benign |
Het |
Lyst |
T |
C |
13: 13,810,426 (GRCm39) |
F699L |
probably benign |
Het |
Matn3 |
T |
A |
12: 9,008,797 (GRCm39) |
D303E |
probably benign |
Het |
Me1 |
A |
G |
9: 86,464,876 (GRCm39) |
Y545H |
probably damaging |
Het |
Mettl3 |
A |
T |
14: 52,537,756 (GRCm39) |
V68E |
probably benign |
Het |
Mptx2 |
T |
C |
1: 173,102,536 (GRCm39) |
N51S |
probably benign |
Het |
Mylk |
A |
G |
16: 34,699,741 (GRCm39) |
D368G |
probably benign |
Het |
Myom2 |
T |
C |
8: 15,131,418 (GRCm39) |
V372A |
possibly damaging |
Het |
Neb |
T |
C |
2: 52,085,433 (GRCm39) |
D5569G |
probably damaging |
Het |
Nefh |
GGGACTTGGCCTCACCTGGGGACTTGGCCTC |
GGGACTTGGCCTCACCTGCGGACTTGGCCTCACCTGGGGACTTGGCCTC |
11: 4,891,030 (GRCm39) |
|
probably benign |
Het |
P4ha2 |
CCAGGTG |
C |
11: 54,001,061 (GRCm39) |
|
probably benign |
Het |
Pop1 |
G |
A |
15: 34,502,583 (GRCm39) |
G90D |
probably damaging |
Het |
Rbm12 |
CC |
CCGGGTATTGTGGGACCAGTTATTGCGGGAGC |
2: 155,937,995 (GRCm39) |
|
probably benign |
Het |
Sertad4 |
T |
C |
1: 192,529,486 (GRCm39) |
Y110C |
probably damaging |
Het |
Setd1a |
GGTAGTGGT |
GGTAGTGGTAGTAGTGGT |
7: 127,384,486 (GRCm39) |
|
probably benign |
Het |
Supt20 |
AGCA |
AGCACCCGCA |
3: 54,635,083 (GRCm39) |
|
probably benign |
Het |
Tcof1 |
AGC |
AGCCGC |
18: 60,968,811 (GRCm39) |
|
probably benign |
Het |
Tecpr1 |
A |
G |
5: 144,154,204 (GRCm39) |
F83S |
probably damaging |
Het |
Triobp |
GCGGGACAGCCCCAGGACTCCCTGTGCCCAACGGGACA |
GCGGGACAGCCCCAGGACTCCCTGTGCCCAACGGGACAGCCCCAGGACTCCCTGTGCCCAACGGGACA |
15: 78,851,227 (GRCm39) |
|
probably benign |
Het |
Vmn1r48 |
A |
T |
6: 90,013,186 (GRCm39) |
M213K |
probably benign |
Het |
Zc3h4 |
CCC |
CCCTGACATGCATCC |
7: 16,163,612 (GRCm39) |
|
probably benign |
Het |
Zscan29 |
T |
C |
2: 120,994,477 (GRCm39) |
N503D |
possibly 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 |
|
R1256:Smarca2
|
UTSW |
19 |
26,659,373 (GRCm39) |
missense |
probably benign |
0.06 |
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 |
|
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 |
|