Other mutations in this stock |
Total: 91 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930505A04Rik |
C |
T |
11: 30,376,349 (GRCm39) |
V173M |
probably damaging |
Het |
9130008F23Rik |
G |
T |
17: 41,191,052 (GRCm39) |
Q126K |
probably benign |
Het |
Abca15 |
C |
A |
7: 120,000,941 (GRCm39) |
N1492K |
probably damaging |
Het |
Afap1l2 |
C |
T |
19: 56,906,472 (GRCm39) |
D402N |
probably damaging |
Het |
Akap11 |
A |
G |
14: 78,750,408 (GRCm39) |
F660L |
probably damaging |
Het |
Bcl3 |
T |
C |
7: 19,554,102 (GRCm39) |
T89A |
probably benign |
Het |
Bub1b |
T |
C |
2: 118,467,251 (GRCm39) |
I858T |
possibly damaging |
Het |
Cdk19 |
A |
G |
10: 40,352,214 (GRCm39) |
D288G |
possibly damaging |
Het |
Cyp2d34 |
T |
A |
15: 82,502,530 (GRCm39) |
D202V |
probably damaging |
Het |
Dip2c |
T |
G |
13: 9,625,259 (GRCm39) |
Y584* |
probably null |
Het |
Dpf3 |
A |
T |
12: 83,378,635 (GRCm39) |
|
probably null |
Het |
Drp2 |
G |
A |
X: 133,342,065 (GRCm39) |
R567H |
probably damaging |
Homo |
Emid1 |
G |
T |
11: 5,081,512 (GRCm39) |
Q212K |
probably benign |
Het |
Esm1 |
C |
T |
13: 113,349,933 (GRCm39) |
Q118* |
probably null |
Het |
Fahd2a |
T |
G |
2: 127,278,284 (GRCm39) |
I308L |
probably benign |
Het |
Fanci |
T |
C |
7: 79,085,126 (GRCm39) |
*851Q |
probably null |
Het |
Fastkd1 |
C |
A |
2: 69,533,084 (GRCm39) |
V428F |
probably damaging |
Het |
Fat2 |
A |
T |
11: 55,173,918 (GRCm39) |
I2265N |
probably damaging |
Het |
Gale |
C |
A |
4: 135,694,171 (GRCm39) |
H191Q |
probably damaging |
Het |
Ghsr |
T |
A |
3: 27,426,403 (GRCm39) |
V153E |
possibly damaging |
Het |
Gpc6 |
A |
G |
14: 117,861,951 (GRCm39) |
N289S |
possibly damaging |
Het |
Hoxb6 |
A |
T |
11: 96,191,537 (GRCm39) |
Y153F |
probably damaging |
Het |
Ints3 |
T |
C |
3: 90,322,814 (GRCm39) |
T139A |
probably benign |
Het |
Irf2bp2 |
A |
G |
8: 127,319,410 (GRCm39) |
S256P |
probably benign |
Het |
Klf4 |
G |
T |
4: 55,530,640 (GRCm39) |
P148Q |
probably damaging |
Het |
Loxl1 |
T |
G |
9: 58,219,820 (GRCm39) |
H117P |
probably damaging |
Het |
Lpl |
A |
G |
8: 69,348,445 (GRCm39) |
K225E |
probably benign |
Het |
Lrba |
T |
A |
3: 86,267,344 (GRCm39) |
V1678D |
probably damaging |
Het |
Med1 |
A |
T |
11: 98,054,730 (GRCm39) |
F398Y |
probably damaging |
Het |
Mfap2 |
T |
C |
4: 140,742,889 (GRCm39) |
*186Q |
probably null |
Het |
Mfsd3 |
T |
C |
15: 76,586,182 (GRCm39) |
L105P |
probably damaging |
Het |
Mlxip |
T |
G |
5: 123,533,357 (GRCm39) |
I122S |
probably damaging |
Het |
Mmrn2 |
A |
T |
14: 34,118,355 (GRCm39) |
Y107F |
probably damaging |
Het |
Mtg1 |
G |
T |
7: 139,720,196 (GRCm39) |
D88Y |
probably null |
Het |
Mutyh |
T |
A |
4: 116,675,132 (GRCm39) |
S426R |
probably benign |
Het |
Myo16 |
C |
T |
8: 10,526,094 (GRCm39) |
T878I |
probably damaging |
Het |
Myo9a |
T |
A |
9: 59,768,755 (GRCm39) |
Y912* |
probably null |
Het |
Ncor1 |
A |
C |
11: 62,234,167 (GRCm39) |
I669R |
probably damaging |
Het |
Ndufs1 |
T |
C |
1: 63,202,935 (GRCm39) |
I210V |
probably benign |
Het |
Nek9 |
A |
G |
12: 85,357,194 (GRCm39) |
C657R |
probably damaging |
Het |
Noct |
C |
T |
3: 51,157,442 (GRCm39) |
T260I |
probably damaging |
Het |
Nr1h4 |
A |
T |
10: 89,334,042 (GRCm39) |
M102K |
probably benign |
Het |
Obscn |
G |
A |
11: 59,015,587 (GRCm39) |
R1054C |
possibly damaging |
Het |
Or10ag58 |
T |
A |
2: 87,265,496 (GRCm39) |
F222I |
probably benign |
Het |
Or1j20 |
C |
A |
2: 36,760,000 (GRCm39) |
Q141K |
probably benign |
Het |
Or2a57 |
A |
G |
6: 43,213,390 (GRCm39) |
M283V |
possibly damaging |
Het |
Or51ah3 |
T |
A |
7: 103,210,524 (GRCm39) |
I280N |
possibly damaging |
Het |
Or52z14 |
A |
T |
7: 103,252,863 (GRCm39) |
M1L |
probably benign |
Het |
Or5p75-ps1 |
G |
A |
7: 108,107,450 (GRCm39) |
M62I |
probably damaging |
Het |
Otol1 |
C |
A |
3: 69,926,211 (GRCm39) |
Q129K |
probably benign |
Het |
Otx1 |
A |
T |
11: 21,948,532 (GRCm39) |
|
probably null |
Het |
Pcdhac2 |
C |
A |
18: 37,279,304 (GRCm39) |
N761K |
probably damaging |
Het |
Pde1c |
A |
T |
6: 56,127,609 (GRCm39) |
M452K |
probably damaging |
Het |
Phkg2 |
T |
C |
7: 127,173,113 (GRCm39) |
Y24H |
probably damaging |
Het |
Pigr |
G |
A |
1: 130,769,554 (GRCm39) |
D122N |
probably benign |
Het |
Prg4 |
C |
T |
1: 150,336,432 (GRCm39) |
C97Y |
probably damaging |
Het |
Ptdss1 |
T |
C |
13: 67,093,352 (GRCm39) |
V64A |
probably benign |
Het |
Ralgapa2 |
T |
C |
2: 146,289,231 (GRCm39) |
K324E |
probably damaging |
Het |
Rfx5 |
G |
A |
3: 94,863,126 (GRCm39) |
V73I |
probably benign |
Het |
Riiad1 |
T |
C |
3: 94,380,170 (GRCm39) |
T42A |
probably benign |
Het |
Rims2 |
T |
C |
15: 39,317,841 (GRCm39) |
V640A |
possibly damaging |
Het |
Rnpep |
G |
T |
1: 135,190,770 (GRCm39) |
S592Y |
possibly damaging |
Het |
Scap |
T |
C |
9: 110,207,458 (GRCm39) |
L431P |
probably damaging |
Het |
Siglec1 |
T |
A |
2: 130,915,281 (GRCm39) |
I1437F |
possibly damaging |
Het |
Skic3 |
T |
A |
13: 76,331,055 (GRCm39) |
M1495K |
probably damaging |
Het |
Skint1 |
T |
C |
4: 111,885,530 (GRCm39) |
|
probably null |
Het |
Slc44a1 |
A |
G |
4: 53,543,644 (GRCm39) |
E396G |
probably damaging |
Het |
Slc4a2 |
T |
C |
5: 24,639,867 (GRCm39) |
F521S |
probably damaging |
Het |
Socs1 |
A |
G |
16: 10,602,549 (GRCm39) |
S63P |
probably benign |
Het |
Spopfm2 |
C |
T |
3: 94,083,623 (GRCm39) |
G63R |
probably damaging |
Het |
Sun1 |
T |
G |
5: 139,211,088 (GRCm39) |
S20A |
possibly damaging |
Het |
Tac4 |
A |
T |
11: 95,156,068 (GRCm39) |
K50* |
probably null |
Het |
Tasor |
T |
A |
14: 27,151,071 (GRCm39) |
W16R |
possibly damaging |
Het |
Tcaf2 |
A |
G |
6: 42,619,574 (GRCm39) |
I151T |
probably damaging |
Het |
Tcf4 |
T |
C |
18: 69,814,840 (GRCm39) |
V587A |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,571,253 (GRCm39) |
K24801* |
probably null |
Het |
Tuba3b |
G |
T |
6: 145,566,999 (GRCm39) |
M413I |
possibly damaging |
Het |
Ufl1 |
C |
T |
4: 25,267,832 (GRCm39) |
A280T |
possibly damaging |
Het |
Ugt2b5 |
T |
A |
5: 87,287,532 (GRCm39) |
I212L |
probably benign |
Het |
Umodl1 |
A |
G |
17: 31,205,459 (GRCm39) |
T685A |
probably benign |
Het |
Uqcrc1 |
T |
A |
9: 108,773,878 (GRCm39) |
V183D |
probably damaging |
Het |
Ush2a |
A |
G |
1: 188,642,917 (GRCm39) |
N4093S |
probably benign |
Het |
Vmn1r167 |
C |
T |
7: 23,204,653 (GRCm39) |
S121N |
probably damaging |
Het |
Vmn1r47 |
A |
G |
6: 89,999,740 (GRCm39) |
S291G |
possibly damaging |
Het |
Vmn2r108 |
A |
G |
17: 20,701,449 (GRCm39) |
V17A |
probably benign |
Het |
Vmn2r58 |
T |
A |
7: 41,487,176 (GRCm39) |
H573L |
probably benign |
Het |
Xirp1 |
C |
T |
9: 119,847,858 (GRCm39) |
V342I |
probably damaging |
Het |
Zfp462 |
A |
G |
4: 55,051,204 (GRCm39) |
M2226V |
possibly damaging |
Het |
Zfp467 |
G |
A |
6: 48,415,963 (GRCm39) |
H230Y |
probably damaging |
Het |
Zfp595 |
T |
A |
13: 67,464,465 (GRCm39) |
K599N |
probably damaging |
Het |
Zfp819 |
C |
A |
7: 43,266,720 (GRCm39) |
T401K |
probably benign |
Het |
|
Other mutations in Smarcc1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01107:Smarcc1
|
APN |
9 |
110,051,005 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01152:Smarcc1
|
APN |
9 |
109,968,693 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL01353:Smarcc1
|
APN |
9 |
109,964,734 (GRCm39) |
missense |
probably benign |
0.07 |
IGL01401:Smarcc1
|
APN |
9 |
109,979,033 (GRCm39) |
missense |
possibly damaging |
0.52 |
IGL01483:Smarcc1
|
APN |
9 |
110,051,128 (GRCm39) |
nonsense |
probably null |
|
IGL01679:Smarcc1
|
APN |
9 |
110,042,598 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02458:Smarcc1
|
APN |
9 |
109,961,194 (GRCm39) |
intron |
probably benign |
|
IGL02498:Smarcc1
|
APN |
9 |
110,020,002 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02605:Smarcc1
|
APN |
9 |
110,051,068 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL03003:Smarcc1
|
APN |
9 |
110,035,168 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03284:Smarcc1
|
APN |
9 |
110,004,142 (GRCm39) |
missense |
probably benign |
0.30 |
R0116:Smarcc1
|
UTSW |
9 |
109,976,172 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0403:Smarcc1
|
UTSW |
9 |
110,066,876 (GRCm39) |
splice site |
probably null |
|
R1436:Smarcc1
|
UTSW |
9 |
109,947,708 (GRCm39) |
unclassified |
probably benign |
|
R1583:Smarcc1
|
UTSW |
9 |
110,042,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R1692:Smarcc1
|
UTSW |
9 |
110,003,072 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1732:Smarcc1
|
UTSW |
9 |
110,014,888 (GRCm39) |
splice site |
probably benign |
|
R1833:Smarcc1
|
UTSW |
9 |
109,982,879 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1881:Smarcc1
|
UTSW |
9 |
110,004,167 (GRCm39) |
missense |
probably damaging |
1.00 |
R2058:Smarcc1
|
UTSW |
9 |
109,947,411 (GRCm39) |
unclassified |
probably benign |
|
R2175:Smarcc1
|
UTSW |
9 |
109,993,877 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2215:Smarcc1
|
UTSW |
9 |
110,066,907 (GRCm39) |
utr 3 prime |
probably benign |
|
R2904:Smarcc1
|
UTSW |
9 |
110,003,043 (GRCm39) |
missense |
possibly damaging |
0.80 |
R3899:Smarcc1
|
UTSW |
9 |
109,947,586 (GRCm39) |
unclassified |
probably benign |
|
R3900:Smarcc1
|
UTSW |
9 |
109,947,586 (GRCm39) |
unclassified |
probably benign |
|
R4012:Smarcc1
|
UTSW |
9 |
109,961,273 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4091:Smarcc1
|
UTSW |
9 |
109,993,897 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4356:Smarcc1
|
UTSW |
9 |
110,025,324 (GRCm39) |
missense |
probably damaging |
0.99 |
R4881:Smarcc1
|
UTSW |
9 |
109,964,696 (GRCm39) |
start gained |
probably benign |
|
R5110:Smarcc1
|
UTSW |
9 |
110,026,852 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5375:Smarcc1
|
UTSW |
9 |
110,020,017 (GRCm39) |
missense |
probably damaging |
0.99 |
R5655:Smarcc1
|
UTSW |
9 |
109,986,412 (GRCm39) |
missense |
probably null |
1.00 |
R5715:Smarcc1
|
UTSW |
9 |
110,025,435 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5767:Smarcc1
|
UTSW |
9 |
109,961,251 (GRCm39) |
intron |
probably benign |
|
R5816:Smarcc1
|
UTSW |
9 |
110,026,712 (GRCm39) |
missense |
possibly damaging |
0.51 |
R6969:Smarcc1
|
UTSW |
9 |
110,025,388 (GRCm39) |
missense |
probably damaging |
1.00 |
R7068:Smarcc1
|
UTSW |
9 |
110,014,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R7211:Smarcc1
|
UTSW |
9 |
109,979,082 (GRCm39) |
missense |
probably damaging |
0.97 |
R7558:Smarcc1
|
UTSW |
9 |
109,976,184 (GRCm39) |
missense |
probably damaging |
0.96 |
R7903:Smarcc1
|
UTSW |
9 |
110,033,334 (GRCm39) |
missense |
probably benign |
0.01 |
R8190:Smarcc1
|
UTSW |
9 |
110,031,602 (GRCm39) |
missense |
probably benign |
|
R8695:Smarcc1
|
UTSW |
9 |
110,002,972 (GRCm39) |
missense |
probably damaging |
0.98 |
R8842:Smarcc1
|
UTSW |
9 |
110,051,199 (GRCm39) |
missense |
possibly damaging |
0.60 |
R9024:Smarcc1
|
UTSW |
9 |
110,015,001 (GRCm39) |
missense |
probably damaging |
0.99 |
R9131:Smarcc1
|
UTSW |
9 |
109,964,710 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9180:Smarcc1
|
UTSW |
9 |
109,964,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R9279:Smarcc1
|
UTSW |
9 |
109,996,792 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9352:Smarcc1
|
UTSW |
9 |
110,035,220 (GRCm39) |
missense |
probably null |
1.00 |
R9538:Smarcc1
|
UTSW |
9 |
109,961,272 (GRCm39) |
missense |
probably benign |
0.00 |
R9645:Smarcc1
|
UTSW |
9 |
109,986,410 (GRCm39) |
missense |
probably damaging |
1.00 |
T0722:Smarcc1
|
UTSW |
9 |
110,035,153 (GRCm39) |
missense |
possibly damaging |
0.86 |
|