Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1600012H06Rik |
T |
C |
17: 15,164,380 (GRCm39) |
L169P |
probably damaging |
Het |
4933405L10Rik |
C |
A |
8: 106,435,567 (GRCm39) |
A75E |
probably benign |
Het |
Acox2 |
C |
A |
14: 8,251,617 (GRCm38) |
M293I |
probably damaging |
Het |
Acp6 |
A |
G |
3: 97,081,123 (GRCm39) |
S288G |
probably benign |
Het |
Arhgef12 |
T |
A |
9: 42,934,137 (GRCm39) |
H127L |
possibly damaging |
Het |
Arid2 |
T |
G |
15: 96,254,678 (GRCm39) |
F175V |
probably damaging |
Het |
Ccdc15 |
G |
A |
9: 37,226,532 (GRCm39) |
Q468* |
probably null |
Het |
Ccdc93 |
T |
C |
1: 121,390,859 (GRCm39) |
I277T |
probably damaging |
Het |
Cdh8 |
T |
C |
8: 99,825,586 (GRCm39) |
|
probably benign |
Het |
Cdipt |
T |
C |
7: 126,578,725 (GRCm39) |
S145P |
possibly damaging |
Het |
Cfap206 |
T |
C |
4: 34,719,610 (GRCm39) |
N268S |
possibly damaging |
Het |
Clcn3 |
A |
T |
8: 61,366,129 (GRCm39) |
N814K |
probably benign |
Het |
Col6a3 |
T |
C |
1: 90,724,293 (GRCm39) |
D2019G |
probably damaging |
Het |
Corin |
C |
A |
5: 72,511,282 (GRCm39) |
G432C |
probably damaging |
Het |
Crppa |
A |
G |
12: 36,597,918 (GRCm39) |
R350G |
probably benign |
Het |
Cyld |
C |
T |
8: 89,432,403 (GRCm39) |
Q134* |
probably null |
Het |
Dhh |
C |
A |
15: 98,795,864 (GRCm39) |
R97L |
probably damaging |
Het |
Dnah5 |
T |
C |
15: 28,449,315 (GRCm39) |
V4239A |
probably benign |
Het |
Dock2 |
T |
C |
11: 34,599,692 (GRCm39) |
I296V |
probably benign |
Het |
Gabbr1 |
T |
C |
17: 37,359,306 (GRCm39) |
|
probably benign |
Het |
Gbp10 |
T |
C |
5: 105,367,815 (GRCm39) |
|
probably null |
Het |
Itgam |
T |
A |
7: 127,711,644 (GRCm39) |
L753Q |
probably damaging |
Het |
Kbtbd12 |
A |
G |
6: 88,590,922 (GRCm39) |
V430A |
probably benign |
Het |
Kdm4a |
A |
G |
4: 118,017,656 (GRCm39) |
V470A |
possibly damaging |
Het |
Larp1b |
A |
T |
3: 40,924,960 (GRCm39) |
T146S |
probably benign |
Het |
Lrrfip2 |
T |
A |
9: 111,028,728 (GRCm39) |
|
probably benign |
Het |
Mier2 |
A |
T |
10: 79,385,418 (GRCm39) |
C137S |
possibly damaging |
Het |
Morc3 |
A |
G |
16: 93,657,455 (GRCm39) |
Y393C |
probably damaging |
Het |
Ms4a7 |
A |
T |
19: 11,299,751 (GRCm39) |
M217K |
possibly damaging |
Het |
Msl1 |
A |
G |
11: 98,696,191 (GRCm39) |
|
probably null |
Het |
Myh2 |
A |
G |
11: 67,083,860 (GRCm39) |
E1546G |
probably benign |
Het |
Nlgn2 |
A |
G |
11: 69,716,675 (GRCm39) |
L622P |
possibly damaging |
Het |
Oga |
T |
A |
19: 45,756,301 (GRCm39) |
E447D |
probably benign |
Het |
Or10q3 |
A |
G |
19: 11,847,888 (GRCm39) |
S231P |
probably benign |
Het |
Or1e33 |
A |
G |
11: 73,738,298 (GRCm39) |
Y218H |
probably damaging |
Het |
Or1j11 |
A |
C |
2: 36,312,105 (GRCm39) |
K232Q |
probably benign |
Het |
Or56b1b |
T |
A |
7: 108,164,343 (GRCm39) |
I220L |
possibly damaging |
Het |
Or5k17 |
T |
C |
16: 58,746,929 (GRCm39) |
M2V |
probably benign |
Het |
Phf20 |
C |
A |
2: 156,118,577 (GRCm39) |
S427* |
probably null |
Het |
Pirt |
G |
A |
11: 66,816,794 (GRCm39) |
S35N |
probably damaging |
Het |
Prss28 |
C |
A |
17: 25,529,011 (GRCm39) |
N117K |
possibly damaging |
Het |
Rbbp8nl |
A |
G |
2: 179,925,104 (GRCm39) |
C34R |
probably damaging |
Het |
Rtn3 |
A |
T |
19: 7,435,241 (GRCm39) |
D231E |
probably damaging |
Het |
Sema5a |
T |
C |
15: 32,474,514 (GRCm39) |
|
probably benign |
Het |
Sh3bp2 |
T |
A |
5: 34,713,347 (GRCm39) |
L196Q |
probably damaging |
Het |
Slc26a9 |
G |
T |
1: 131,685,256 (GRCm39) |
D325Y |
probably damaging |
Het |
Slc4a1 |
A |
G |
11: 102,244,729 (GRCm39) |
V622A |
probably benign |
Het |
Thbd |
A |
G |
2: 148,249,016 (GRCm39) |
V284A |
probably benign |
Het |
Tmc5 |
T |
C |
7: 118,251,733 (GRCm39) |
F609L |
possibly damaging |
Het |
Tnr |
T |
C |
1: 159,695,576 (GRCm39) |
|
probably benign |
Het |
Ttc17 |
A |
T |
2: 94,163,177 (GRCm39) |
Y881* |
probably null |
Het |
Ttc41 |
A |
T |
10: 86,612,488 (GRCm39) |
T1254S |
probably benign |
Het |
Ttn |
C |
T |
2: 76,640,347 (GRCm39) |
D13754N |
probably damaging |
Het |
Vmn2r16 |
T |
A |
5: 109,511,762 (GRCm39) |
F656L |
probably damaging |
Het |
Wdr19 |
A |
G |
5: 65,382,709 (GRCm39) |
I478V |
probably damaging |
Het |
Zan |
T |
C |
5: 137,379,116 (GRCm39) |
|
probably benign |
Het |
Zp2 |
T |
A |
7: 119,737,414 (GRCm39) |
D258V |
probably damaging |
Het |
|
Other mutations in Abca1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00429:Abca1
|
APN |
4 |
53,059,255 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00778:Abca1
|
APN |
4 |
53,086,132 (GRCm39) |
missense |
probably benign |
|
IGL01013:Abca1
|
APN |
4 |
53,038,185 (GRCm39) |
nonsense |
probably null |
|
IGL01510:Abca1
|
APN |
4 |
53,143,979 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01608:Abca1
|
APN |
4 |
53,038,158 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02048:Abca1
|
APN |
4 |
53,069,831 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02249:Abca1
|
APN |
4 |
53,068,739 (GRCm39) |
nonsense |
probably null |
|
IGL02569:Abca1
|
APN |
4 |
53,034,061 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02622:Abca1
|
APN |
4 |
53,034,046 (GRCm39) |
missense |
probably damaging |
0.99 |
R6720_abca1_529
|
UTSW |
4 |
53,083,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R0042:Abca1
|
UTSW |
4 |
53,059,245 (GRCm39) |
splice site |
probably benign |
|
R0042:Abca1
|
UTSW |
4 |
53,059,245 (GRCm39) |
splice site |
probably benign |
|
R0050:Abca1
|
UTSW |
4 |
53,069,910 (GRCm39) |
splice site |
probably benign |
|
R0107:Abca1
|
UTSW |
4 |
53,080,834 (GRCm39) |
missense |
probably benign |
0.00 |
R0127:Abca1
|
UTSW |
4 |
53,067,155 (GRCm39) |
missense |
probably benign |
0.00 |
R0178:Abca1
|
UTSW |
4 |
53,081,953 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0207:Abca1
|
UTSW |
4 |
53,086,039 (GRCm39) |
missense |
probably damaging |
0.97 |
R0267:Abca1
|
UTSW |
4 |
53,046,105 (GRCm39) |
missense |
probably damaging |
1.00 |
R0269:Abca1
|
UTSW |
4 |
53,044,228 (GRCm39) |
missense |
probably benign |
|
R0586:Abca1
|
UTSW |
4 |
53,092,860 (GRCm39) |
missense |
probably benign |
0.00 |
R0587:Abca1
|
UTSW |
4 |
53,107,035 (GRCm39) |
missense |
probably benign |
0.00 |
R1403:Abca1
|
UTSW |
4 |
53,059,253 (GRCm39) |
splice site |
probably benign |
|
R1404:Abca1
|
UTSW |
4 |
53,059,253 (GRCm39) |
splice site |
probably benign |
|
R1405:Abca1
|
UTSW |
4 |
53,059,253 (GRCm39) |
splice site |
probably benign |
|
R1558:Abca1
|
UTSW |
4 |
53,092,887 (GRCm39) |
missense |
probably null |
0.00 |
R1655:Abca1
|
UTSW |
4 |
53,050,964 (GRCm39) |
missense |
probably benign |
|
R1662:Abca1
|
UTSW |
4 |
53,090,251 (GRCm39) |
splice site |
probably null |
|
R1769:Abca1
|
UTSW |
4 |
53,074,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R1898:Abca1
|
UTSW |
4 |
53,071,977 (GRCm39) |
missense |
probably benign |
0.08 |
R1945:Abca1
|
UTSW |
4 |
53,061,509 (GRCm39) |
frame shift |
probably null |
|
R1966:Abca1
|
UTSW |
4 |
53,050,409 (GRCm39) |
missense |
probably damaging |
1.00 |
R2055:Abca1
|
UTSW |
4 |
53,069,881 (GRCm39) |
missense |
probably benign |
|
R2185:Abca1
|
UTSW |
4 |
53,089,830 (GRCm39) |
missense |
probably benign |
0.12 |
R2202:Abca1
|
UTSW |
4 |
53,090,291 (GRCm39) |
missense |
probably damaging |
0.96 |
R2203:Abca1
|
UTSW |
4 |
53,090,291 (GRCm39) |
missense |
probably damaging |
0.96 |
R2204:Abca1
|
UTSW |
4 |
53,090,291 (GRCm39) |
missense |
probably damaging |
0.96 |
R3056:Abca1
|
UTSW |
4 |
53,127,626 (GRCm39) |
missense |
probably benign |
|
R3849:Abca1
|
UTSW |
4 |
53,061,481 (GRCm39) |
splice site |
probably benign |
|
R3850:Abca1
|
UTSW |
4 |
53,061,481 (GRCm39) |
splice site |
probably benign |
|
R3906:Abca1
|
UTSW |
4 |
53,067,151 (GRCm39) |
missense |
possibly damaging |
0.84 |
R3908:Abca1
|
UTSW |
4 |
53,067,151 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4050:Abca1
|
UTSW |
4 |
53,044,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R4204:Abca1
|
UTSW |
4 |
53,090,369 (GRCm39) |
missense |
probably benign |
0.00 |
R4225:Abca1
|
UTSW |
4 |
53,085,106 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4577:Abca1
|
UTSW |
4 |
53,062,568 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4979:Abca1
|
UTSW |
4 |
53,085,092 (GRCm39) |
splice site |
probably null |
|
R5022:Abca1
|
UTSW |
4 |
53,041,570 (GRCm39) |
frame shift |
probably null |
|
R5168:Abca1
|
UTSW |
4 |
53,086,070 (GRCm39) |
missense |
probably benign |
|
R5363:Abca1
|
UTSW |
4 |
53,132,963 (GRCm39) |
missense |
probably benign |
0.00 |
R5439:Abca1
|
UTSW |
4 |
53,042,381 (GRCm39) |
missense |
possibly damaging |
0.55 |
R5604:Abca1
|
UTSW |
4 |
53,067,168 (GRCm39) |
splice site |
probably null |
|
R5614:Abca1
|
UTSW |
4 |
53,046,132 (GRCm39) |
missense |
probably damaging |
1.00 |
R5810:Abca1
|
UTSW |
4 |
53,079,631 (GRCm39) |
missense |
probably benign |
|
R6001:Abca1
|
UTSW |
4 |
53,075,555 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6151:Abca1
|
UTSW |
4 |
53,085,261 (GRCm39) |
missense |
probably benign |
|
R6185:Abca1
|
UTSW |
4 |
53,078,089 (GRCm39) |
missense |
probably benign |
0.31 |
R6262:Abca1
|
UTSW |
4 |
53,092,917 (GRCm39) |
missense |
probably benign |
0.01 |
R6455:Abca1
|
UTSW |
4 |
53,042,376 (GRCm39) |
missense |
probably damaging |
0.98 |
R6472:Abca1
|
UTSW |
4 |
53,085,991 (GRCm39) |
critical splice donor site |
probably null |
|
R6564:Abca1
|
UTSW |
4 |
53,034,031 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6720:Abca1
|
UTSW |
4 |
53,083,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R6903:Abca1
|
UTSW |
4 |
53,143,952 (GRCm39) |
missense |
probably benign |
0.17 |
R6960:Abca1
|
UTSW |
4 |
53,072,924 (GRCm39) |
missense |
probably benign |
0.00 |
R7065:Abca1
|
UTSW |
4 |
53,074,233 (GRCm39) |
missense |
probably damaging |
0.98 |
R7142:Abca1
|
UTSW |
4 |
53,082,050 (GRCm39) |
missense |
probably damaging |
1.00 |
R7322:Abca1
|
UTSW |
4 |
53,067,151 (GRCm39) |
missense |
probably damaging |
0.97 |
R7520:Abca1
|
UTSW |
4 |
53,078,114 (GRCm39) |
missense |
probably benign |
|
R7547:Abca1
|
UTSW |
4 |
53,109,269 (GRCm39) |
missense |
probably benign |
0.02 |
R7793:Abca1
|
UTSW |
4 |
53,042,367 (GRCm39) |
missense |
not run |
|
R7863:Abca1
|
UTSW |
4 |
53,107,179 (GRCm39) |
missense |
probably benign |
|
R7877:Abca1
|
UTSW |
4 |
53,046,135 (GRCm39) |
missense |
possibly damaging |
0.55 |
R8010:Abca1
|
UTSW |
4 |
53,127,600 (GRCm39) |
missense |
probably benign |
|
R8058:Abca1
|
UTSW |
4 |
53,081,954 (GRCm39) |
missense |
possibly damaging |
0.60 |
R8181:Abca1
|
UTSW |
4 |
53,059,303 (GRCm39) |
missense |
probably benign |
0.21 |
R8471:Abca1
|
UTSW |
4 |
53,044,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R8774:Abca1
|
UTSW |
4 |
53,090,358 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8774-TAIL:Abca1
|
UTSW |
4 |
53,090,358 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8806:Abca1
|
UTSW |
4 |
53,084,520 (GRCm39) |
missense |
probably benign |
0.17 |
R8841:Abca1
|
UTSW |
4 |
53,143,925 (GRCm39) |
splice site |
probably benign |
|
R9081:Abca1
|
UTSW |
4 |
53,109,162 (GRCm39) |
critical splice donor site |
probably null |
|
R9483:Abca1
|
UTSW |
4 |
53,060,351 (GRCm39) |
missense |
probably benign |
0.11 |
R9532:Abca1
|
UTSW |
4 |
53,109,284 (GRCm39) |
missense |
probably benign |
|
R9621:Abca1
|
UTSW |
4 |
53,092,918 (GRCm39) |
missense |
probably benign |
0.00 |
R9638:Abca1
|
UTSW |
4 |
53,092,806 (GRCm39) |
missense |
probably damaging |
0.96 |
RF005:Abca1
|
UTSW |
4 |
53,049,125 (GRCm39) |
missense |
probably damaging |
0.97 |
RF024:Abca1
|
UTSW |
4 |
53,049,125 (GRCm39) |
missense |
probably damaging |
0.97 |
X0023:Abca1
|
UTSW |
4 |
53,049,038 (GRCm39) |
missense |
possibly damaging |
0.91 |
Z1177:Abca1
|
UTSW |
4 |
53,086,133 (GRCm39) |
missense |
possibly damaging |
0.73 |
Z1177:Abca1
|
UTSW |
4 |
53,080,799 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Abca1
|
UTSW |
4 |
53,079,584 (GRCm39) |
missense |
probably benign |
0.00 |
|