Other mutations in this stock |
Total: 112 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921524L21Rik |
G |
C |
18: 6,623,470 (GRCm39) |
R60P |
possibly damaging |
Het |
Aox1 |
T |
A |
1: 58,393,354 (GRCm39) |
C1199S |
probably benign |
Het |
Arhgap18 |
G |
A |
10: 26,763,857 (GRCm39) |
M482I |
probably damaging |
Het |
Arhgap18 |
G |
T |
10: 26,763,858 (GRCm39) |
A483S |
probably damaging |
Het |
Arid4a |
G |
A |
12: 71,122,112 (GRCm39) |
S509N |
probably benign |
Het |
BC051019 |
T |
C |
7: 109,322,381 (GRCm39) |
T38A |
probably benign |
Het |
Bcam |
T |
C |
7: 19,499,543 (GRCm39) |
N192S |
probably null |
Het |
Bend5 |
A |
T |
4: 111,311,438 (GRCm39) |
K351* |
probably null |
Het |
Bicdl2 |
T |
A |
17: 23,884,923 (GRCm39) |
M208K |
probably damaging |
Het |
Ccp110 |
A |
T |
7: 118,325,247 (GRCm39) |
|
probably null |
Het |
Cdc6 |
A |
T |
11: 98,803,043 (GRCm39) |
T328S |
probably damaging |
Het |
Cdk5rap2 |
G |
T |
4: 70,225,470 (GRCm39) |
N558K |
probably benign |
Het |
Cdkn1c |
C |
T |
7: 143,012,858 (GRCm39) |
R146K |
probably benign |
Het |
Ceacam18 |
G |
A |
7: 43,297,918 (GRCm39) |
C371Y |
probably benign |
Het |
Cep95 |
T |
A |
11: 106,697,177 (GRCm39) |
C233* |
probably null |
Het |
Chrnd |
A |
G |
1: 87,122,650 (GRCm39) |
I144V |
probably benign |
Het |
Col6a4 |
T |
A |
9: 105,957,299 (GRCm39) |
Q175L |
probably benign |
Het |
Cym |
A |
T |
3: 107,120,816 (GRCm39) |
V263E |
probably damaging |
Het |
Cyp2a4 |
G |
T |
7: 26,012,197 (GRCm39) |
V327F |
possibly damaging |
Het |
Dhx29 |
T |
A |
13: 113,084,774 (GRCm39) |
M664K |
probably damaging |
Het |
Dlec1 |
T |
G |
9: 118,975,075 (GRCm39) |
|
probably null |
Het |
Dna2 |
T |
C |
10: 62,792,863 (GRCm39) |
Y293H |
probably benign |
Het |
Dnase1l3 |
T |
A |
14: 7,974,104 (GRCm38) |
N196Y |
probably damaging |
Het |
Eea1 |
T |
A |
10: 95,832,822 (GRCm39) |
D222E |
probably damaging |
Het |
Efcab14 |
A |
T |
4: 115,610,116 (GRCm39) |
|
probably null |
Het |
Entpd5 |
C |
T |
12: 84,432,985 (GRCm39) |
R189H |
probably benign |
Het |
Exoc4 |
A |
T |
6: 33,734,985 (GRCm39) |
K534M |
probably damaging |
Het |
Extl1 |
T |
A |
4: 134,098,449 (GRCm39) |
Y194F |
probably benign |
Het |
Eya1 |
A |
G |
1: 14,323,299 (GRCm39) |
L161S |
possibly damaging |
Het |
Fam163b |
T |
C |
2: 27,002,874 (GRCm39) |
E41G |
possibly damaging |
Het |
Fam180a |
A |
C |
6: 35,292,287 (GRCm39) |
S40A |
probably benign |
Het |
Fbxl4 |
T |
C |
4: 22,385,950 (GRCm39) |
S186P |
probably benign |
Het |
Fbxw19 |
A |
T |
9: 109,323,840 (GRCm39) |
L45* |
probably null |
Het |
Fgf14 |
G |
T |
14: 124,913,924 (GRCm39) |
T69N |
probably benign |
Het |
Flt1 |
A |
G |
5: 147,609,519 (GRCm39) |
Y432H |
probably damaging |
Het |
Frmd4b |
A |
T |
6: 97,283,725 (GRCm39) |
L374Q |
possibly damaging |
Het |
G6pc2 |
T |
A |
2: 69,053,321 (GRCm39) |
V125D |
probably damaging |
Het |
Gm10033 |
T |
C |
8: 69,826,210 (GRCm39) |
I119M |
unknown |
Het |
Gna15 |
A |
T |
10: 81,347,954 (GRCm39) |
L164Q |
probably damaging |
Het |
Gnaz |
C |
A |
10: 74,827,702 (GRCm39) |
D151E |
possibly damaging |
Het |
Has1 |
T |
C |
17: 18,070,562 (GRCm39) |
T120A |
probably benign |
Het |
Hectd4 |
T |
A |
5: 121,496,366 (GRCm39) |
D3919E |
possibly damaging |
Het |
Hs3st5 |
A |
G |
10: 36,709,165 (GRCm39) |
I233M |
probably benign |
Het |
Ilf3 |
T |
C |
9: 21,314,438 (GRCm39) |
|
probably benign |
Het |
Inpp5b |
T |
A |
4: 124,687,069 (GRCm39) |
L765* |
probably null |
Het |
Insr |
A |
T |
8: 3,209,561 (GRCm39) |
I1174N |
probably damaging |
Het |
Kash5 |
T |
A |
7: 44,838,227 (GRCm39) |
|
probably null |
Het |
Kcnq3 |
A |
G |
15: 65,877,755 (GRCm39) |
L445P |
probably damaging |
Het |
Kctd20 |
A |
T |
17: 29,181,824 (GRCm39) |
N159Y |
probably damaging |
Het |
Kctd20 |
A |
T |
17: 29,185,755 (GRCm39) |
D366V |
probably damaging |
Het |
Klk15 |
T |
C |
7: 43,587,757 (GRCm39) |
|
probably benign |
Het |
Lama4 |
T |
G |
10: 38,979,497 (GRCm39) |
N1658K |
possibly damaging |
Het |
Lonrf2 |
G |
A |
1: 38,852,357 (GRCm39) |
P165S |
probably benign |
Het |
Mas1 |
T |
C |
17: 13,060,586 (GRCm39) |
Y279C |
probably damaging |
Het |
Mast2 |
G |
T |
4: 116,164,156 (GRCm39) |
D1747E |
probably damaging |
Het |
Mest |
G |
A |
6: 30,745,138 (GRCm39) |
M235I |
probably benign |
Het |
Mfsd6 |
A |
G |
1: 52,699,964 (GRCm39) |
|
probably null |
Het |
Mllt10 |
T |
A |
2: 18,167,657 (GRCm39) |
S449R |
probably damaging |
Het |
Mon2 |
T |
A |
10: 122,849,668 (GRCm39) |
T1211S |
probably benign |
Het |
Mrnip |
G |
A |
11: 50,067,688 (GRCm39) |
C27Y |
probably damaging |
Het |
Myh15 |
A |
T |
16: 48,983,498 (GRCm39) |
T1538S |
probably benign |
Het |
Nfatc2ip |
A |
G |
7: 125,989,634 (GRCm39) |
V250A |
probably benign |
Het |
Npy1r |
A |
G |
8: 67,157,177 (GRCm39) |
D199G |
possibly damaging |
Het |
Numbl |
A |
G |
7: 26,980,379 (GRCm39) |
T454A |
probably benign |
Het |
Nutm2 |
T |
G |
13: 50,627,152 (GRCm39) |
F436V |
probably damaging |
Het |
Opa1 |
T |
C |
16: 29,439,628 (GRCm39) |
S773P |
probably benign |
Het |
Or12e1 |
T |
A |
2: 87,022,042 (GRCm39) |
S4T |
probably benign |
Het |
Or2d3 |
A |
T |
7: 106,491,184 (GRCm39) |
|
probably null |
Het |
Or2d3 |
G |
T |
7: 106,491,185 (GRCm39) |
L44M |
probably damaging |
Het |
Or2r11 |
A |
G |
6: 42,437,611 (GRCm39) |
L114S |
probably damaging |
Het |
Or2t48 |
A |
G |
11: 58,420,602 (GRCm39) |
L70P |
probably damaging |
Het |
Or51b17 |
A |
G |
7: 103,542,484 (GRCm39) |
S153P |
probably benign |
Het |
Or51m1 |
C |
T |
7: 103,578,932 (GRCm39) |
R301* |
probably null |
Het |
Or52e7 |
A |
G |
7: 104,685,157 (GRCm39) |
S251G |
probably benign |
Het |
Or52i2 |
A |
G |
7: 102,319,508 (GRCm39) |
Y127C |
probably damaging |
Het |
Or8b12c |
T |
A |
9: 37,715,599 (GRCm39) |
Y131N |
probably damaging |
Het |
Pde8a |
G |
C |
7: 80,950,471 (GRCm39) |
|
probably null |
Het |
Pgam1 |
T |
C |
19: 41,906,144 (GRCm39) |
F232S |
probably damaging |
Het |
Pgk1 |
T |
A |
X: 105,243,914 (GRCm39) |
V303E |
possibly damaging |
Het |
Pirb |
A |
T |
7: 3,720,189 (GRCm39) |
C395S |
probably damaging |
Het |
Plxnc1 |
C |
T |
10: 94,680,184 (GRCm39) |
V824I |
probably benign |
Het |
Ppp6r1 |
A |
G |
7: 4,636,691 (GRCm39) |
|
probably null |
Het |
Rapgef4 |
C |
A |
2: 72,056,131 (GRCm39) |
|
probably benign |
Het |
Rars1 |
T |
A |
11: 35,700,465 (GRCm39) |
T539S |
probably damaging |
Het |
Rbm44 |
G |
T |
1: 91,081,679 (GRCm39) |
|
probably null |
Het |
Samd4b |
A |
G |
7: 28,113,317 (GRCm39) |
I216T |
probably benign |
Het |
Serpine2 |
A |
C |
1: 79,794,532 (GRCm39) |
F134V |
probably damaging |
Het |
Shmt1 |
A |
G |
11: 60,683,790 (GRCm39) |
Y341H |
probably damaging |
Het |
Slc23a2 |
C |
A |
2: 131,917,561 (GRCm39) |
V226F |
probably benign |
Het |
Slc23a4 |
A |
G |
6: 34,933,896 (GRCm39) |
I69T |
probably damaging |
Het |
Slc37a1 |
C |
A |
17: 31,552,652 (GRCm39) |
T319K |
possibly damaging |
Het |
Slc6a4 |
A |
T |
11: 76,904,078 (GRCm39) |
T178S |
probably damaging |
Het |
Spag17 |
A |
T |
3: 99,934,668 (GRCm39) |
Y650F |
possibly damaging |
Het |
Stab2 |
C |
T |
10: 86,838,872 (GRCm39) |
G65S |
probably damaging |
Het |
Stambpl1 |
C |
G |
19: 34,204,121 (GRCm39) |
N70K |
probably damaging |
Het |
Stip1 |
C |
A |
19: 6,999,165 (GRCm39) |
C471F |
probably damaging |
Het |
Taf1 |
T |
C |
X: 100,584,500 (GRCm39) |
S223P |
probably benign |
Het |
Tchh |
C |
A |
3: 93,350,882 (GRCm39) |
N107K |
possibly damaging |
Het |
Tenm3 |
A |
C |
8: 48,685,139 (GRCm39) |
H2432Q |
probably damaging |
Het |
Tmem243 |
A |
G |
5: 9,168,548 (GRCm39) |
N110S |
probably damaging |
Het |
Toe1 |
A |
T |
4: 116,662,076 (GRCm39) |
I306F |
probably benign |
Het |
Trank1 |
G |
A |
9: 111,221,995 (GRCm39) |
V2911M |
probably damaging |
Het |
Trpm4 |
A |
G |
7: 44,958,036 (GRCm39) |
I811T |
probably damaging |
Het |
Tspear |
T |
A |
10: 77,710,950 (GRCm39) |
|
probably null |
Het |
Ttc28 |
A |
T |
5: 111,425,034 (GRCm39) |
I1589F |
possibly damaging |
Het |
Tubgcp3 |
A |
G |
8: 12,699,686 (GRCm39) |
|
probably benign |
Het |
U2af2 |
C |
A |
7: 5,070,544 (GRCm39) |
R78S |
probably benign |
Het |
Wdr17 |
A |
T |
8: 55,126,689 (GRCm39) |
D388E |
possibly damaging |
Het |
Wdr3 |
A |
T |
3: 100,061,186 (GRCm39) |
S261T |
probably benign |
Het |
Zfp667 |
A |
G |
7: 6,308,066 (GRCm39) |
N245D |
possibly damaging |
Het |
Zfp692 |
A |
G |
11: 58,201,002 (GRCm39) |
|
probably benign |
Het |
Zfp729a |
T |
C |
13: 67,767,370 (GRCm39) |
H953R |
probably benign |
Het |
|
Other mutations in Smarca4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01380:Smarca4
|
APN |
9 |
21,590,369 (GRCm39) |
missense |
probably benign |
0.30 |
IGL01694:Smarca4
|
APN |
9 |
21,577,166 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02147:Smarca4
|
APN |
9 |
21,546,999 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02417:Smarca4
|
APN |
9 |
21,612,386 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02421:Smarca4
|
APN |
9 |
21,550,535 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02550:Smarca4
|
APN |
9 |
21,597,418 (GRCm39) |
missense |
probably benign |
0.25 |
IGL02794:Smarca4
|
APN |
9 |
21,584,638 (GRCm39) |
splice site |
probably benign |
|
IGL03030:Smarca4
|
APN |
9 |
21,547,132 (GRCm39) |
missense |
probably benign |
0.14 |
IGL03037:Smarca4
|
APN |
9 |
21,544,231 (GRCm39) |
unclassified |
probably benign |
|
IGL03069:Smarca4
|
APN |
9 |
21,547,132 (GRCm39) |
missense |
probably benign |
0.14 |
IGL03355:Smarca4
|
APN |
9 |
21,547,132 (GRCm39) |
missense |
probably benign |
0.14 |
R0123:Smarca4
|
UTSW |
9 |
21,548,620 (GRCm39) |
missense |
probably damaging |
1.00 |
R0134:Smarca4
|
UTSW |
9 |
21,548,620 (GRCm39) |
missense |
probably damaging |
1.00 |
R0230:Smarca4
|
UTSW |
9 |
21,612,168 (GRCm39) |
missense |
probably damaging |
0.99 |
R0269:Smarca4
|
UTSW |
9 |
21,547,497 (GRCm39) |
missense |
probably benign |
0.09 |
R0631:Smarca4
|
UTSW |
9 |
21,570,280 (GRCm39) |
splice site |
probably benign |
|
R0665:Smarca4
|
UTSW |
9 |
21,612,239 (GRCm39) |
small deletion |
probably benign |
|
R0726:Smarca4
|
UTSW |
9 |
21,611,435 (GRCm39) |
critical splice donor site |
probably null |
|
R0801:Smarca4
|
UTSW |
9 |
21,553,850 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0918:Smarca4
|
UTSW |
9 |
21,547,511 (GRCm39) |
missense |
probably benign |
0.16 |
R1411:Smarca4
|
UTSW |
9 |
21,570,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R1604:Smarca4
|
UTSW |
9 |
21,612,239 (GRCm39) |
small deletion |
probably benign |
|
R2004:Smarca4
|
UTSW |
9 |
21,588,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R2031:Smarca4
|
UTSW |
9 |
21,597,358 (GRCm39) |
missense |
possibly damaging |
0.68 |
R2211:Smarca4
|
UTSW |
9 |
21,597,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R2512:Smarca4
|
UTSW |
9 |
21,546,994 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2875:Smarca4
|
UTSW |
9 |
21,553,876 (GRCm39) |
missense |
possibly damaging |
0.55 |
R3786:Smarca4
|
UTSW |
9 |
21,583,355 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4829:Smarca4
|
UTSW |
9 |
21,550,623 (GRCm39) |
missense |
probably damaging |
0.97 |
R5084:Smarca4
|
UTSW |
9 |
21,572,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R5222:Smarca4
|
UTSW |
9 |
21,567,002 (GRCm39) |
missense |
probably benign |
0.01 |
R5785:Smarca4
|
UTSW |
9 |
21,597,322 (GRCm39) |
missense |
probably damaging |
0.99 |
R5844:Smarca4
|
UTSW |
9 |
21,589,238 (GRCm39) |
intron |
probably benign |
|
R5964:Smarca4
|
UTSW |
9 |
21,558,726 (GRCm39) |
missense |
probably benign |
0.00 |
R6001:Smarca4
|
UTSW |
9 |
21,544,205 (GRCm39) |
unclassified |
probably benign |
|
R6072:Smarca4
|
UTSW |
9 |
21,611,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R6254:Smarca4
|
UTSW |
9 |
21,611,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R6320:Smarca4
|
UTSW |
9 |
21,548,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R6353:Smarca4
|
UTSW |
9 |
21,590,445 (GRCm39) |
critical splice donor site |
probably null |
|
R6461:Smarca4
|
UTSW |
9 |
21,590,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R6886:Smarca4
|
UTSW |
9 |
21,570,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R7098:Smarca4
|
UTSW |
9 |
21,546,116 (GRCm39) |
missense |
probably benign |
0.10 |
R7253:Smarca4
|
UTSW |
9 |
21,570,256 (GRCm39) |
missense |
probably benign |
0.01 |
R7307:Smarca4
|
UTSW |
9 |
21,550,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R7382:Smarca4
|
UTSW |
9 |
21,570,229 (GRCm39) |
missense |
probably damaging |
0.98 |
R7445:Smarca4
|
UTSW |
9 |
21,597,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R7535:Smarca4
|
UTSW |
9 |
21,558,921 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7573:Smarca4
|
UTSW |
9 |
21,550,371 (GRCm39) |
splice site |
probably null |
|
R7644:Smarca4
|
UTSW |
9 |
21,566,950 (GRCm39) |
missense |
probably benign |
0.00 |
R7734:Smarca4
|
UTSW |
9 |
21,578,658 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7833:Smarca4
|
UTSW |
9 |
21,558,655 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8085:Smarca4
|
UTSW |
9 |
21,570,108 (GRCm39) |
splice site |
probably null |
|
R8119:Smarca4
|
UTSW |
9 |
21,558,922 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8320:Smarca4
|
UTSW |
9 |
21,588,798 (GRCm39) |
missense |
probably benign |
0.10 |
R8445:Smarca4
|
UTSW |
9 |
21,612,239 (GRCm39) |
small deletion |
probably benign |
|
R8493:Smarca4
|
UTSW |
9 |
21,570,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R8748:Smarca4
|
UTSW |
9 |
21,546,164 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8788:Smarca4
|
UTSW |
9 |
21,550,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R8817:Smarca4
|
UTSW |
9 |
21,547,497 (GRCm39) |
missense |
probably benign |
0.04 |
R9241:Smarca4
|
UTSW |
9 |
21,550,604 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9446:Smarca4
|
UTSW |
9 |
21,547,155 (GRCm39) |
missense |
unknown |
|
R9570:Smarca4
|
UTSW |
9 |
21,580,849 (GRCm39) |
missense |
probably damaging |
1.00 |
R9727:Smarca4
|
UTSW |
9 |
21,611,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R9801:Smarca4
|
UTSW |
9 |
21,586,397 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Smarca4
|
UTSW |
9 |
21,614,253 (GRCm39) |
nonsense |
probably null |
|
|