Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acr |
T |
A |
15: 89,458,535 (GRCm39) |
H405Q |
probably benign |
Het |
Adad1 |
T |
C |
3: 37,137,322 (GRCm39) |
|
probably benign |
Het |
Alox5ap |
T |
C |
5: 149,216,069 (GRCm39) |
|
probably benign |
Het |
Ank2 |
T |
C |
3: 126,730,280 (GRCm39) |
D3568G |
probably damaging |
Het |
Atl3 |
T |
G |
19: 7,506,388 (GRCm39) |
I306S |
probably damaging |
Het |
Atr |
T |
A |
9: 95,809,409 (GRCm39) |
|
probably benign |
Het |
Ccnb2 |
A |
G |
9: 70,326,335 (GRCm39) |
V34A |
probably benign |
Het |
Cdh12 |
A |
C |
15: 21,537,763 (GRCm39) |
|
probably benign |
Het |
Cib1 |
C |
T |
7: 79,880,126 (GRCm39) |
V45M |
probably benign |
Het |
Col6a6 |
T |
C |
9: 105,657,896 (GRCm39) |
E772G |
possibly damaging |
Het |
Dmxl1 |
C |
A |
18: 49,997,102 (GRCm39) |
T466K |
probably benign |
Het |
Dym |
T |
C |
18: 75,258,610 (GRCm39) |
|
probably null |
Het |
Enpp3 |
A |
C |
10: 24,650,722 (GRCm39) |
F805V |
probably damaging |
Het |
Eya1 |
T |
C |
1: 14,254,713 (GRCm39) |
D373G |
probably damaging |
Het |
Gpr179 |
C |
T |
11: 97,225,757 (GRCm39) |
V2133I |
probably benign |
Het |
Grb10 |
G |
T |
11: 11,886,798 (GRCm39) |
H435Q |
probably damaging |
Het |
Gzmm |
T |
C |
10: 79,530,399 (GRCm39) |
I190T |
probably benign |
Het |
Helt |
T |
C |
8: 46,745,433 (GRCm39) |
Y150C |
probably damaging |
Het |
Hrg |
A |
T |
16: 22,779,886 (GRCm39) |
|
probably benign |
Het |
Il17ra |
T |
C |
6: 120,449,086 (GRCm39) |
|
probably benign |
Het |
Inhbc |
A |
G |
10: 127,193,302 (GRCm39) |
I238T |
probably benign |
Het |
Itgb3 |
A |
G |
11: 104,557,966 (GRCm39) |
T787A |
possibly damaging |
Het |
Jakmip2 |
T |
G |
18: 43,685,210 (GRCm39) |
|
probably benign |
Het |
Krt4 |
T |
G |
15: 101,831,187 (GRCm39) |
|
probably benign |
Het |
Lgsn |
C |
T |
1: 31,229,534 (GRCm39) |
T85I |
probably benign |
Het |
Metap1 |
C |
T |
3: 138,177,918 (GRCm39) |
V217I |
probably benign |
Het |
Mib2 |
A |
T |
4: 155,743,897 (GRCm39) |
C48* |
probably null |
Het |
Mroh4 |
T |
A |
15: 74,482,154 (GRCm39) |
I768F |
probably damaging |
Het |
Npas3 |
T |
A |
12: 54,095,624 (GRCm39) |
D361E |
probably damaging |
Het |
Obscn |
A |
G |
11: 58,943,411 (GRCm39) |
L4246P |
probably damaging |
Het |
Or4a78 |
A |
C |
2: 89,497,798 (GRCm39) |
V144G |
probably benign |
Het |
Or7e169 |
A |
G |
9: 19,757,075 (GRCm39) |
M280T |
probably benign |
Het |
Or8h7 |
A |
G |
2: 86,720,835 (GRCm39) |
I228T |
probably damaging |
Het |
P4hb |
G |
A |
11: 120,459,092 (GRCm39) |
R134C |
probably damaging |
Het |
Plcb3 |
T |
C |
19: 6,943,788 (GRCm39) |
D71G |
probably damaging |
Het |
Prex2 |
T |
A |
1: 11,150,305 (GRCm39) |
V159E |
probably damaging |
Het |
Prpsap1 |
T |
A |
11: 116,370,482 (GRCm39) |
K158N |
probably benign |
Het |
Prr35 |
C |
A |
17: 26,166,956 (GRCm39) |
E194* |
probably null |
Het |
Ptger1 |
G |
T |
8: 84,394,795 (GRCm39) |
V91L |
probably benign |
Het |
Rdh10 |
T |
C |
1: 16,178,260 (GRCm39) |
|
probably benign |
Het |
Rgs9bp |
C |
A |
7: 35,284,458 (GRCm39) |
R63L |
probably damaging |
Het |
Slc13a5 |
A |
T |
11: 72,149,940 (GRCm39) |
V173E |
probably benign |
Het |
Spata31 |
A |
T |
13: 65,070,377 (GRCm39) |
I842L |
probably benign |
Het |
Stk32b |
A |
C |
5: 37,874,092 (GRCm39) |
D13E |
probably benign |
Het |
Svep1 |
T |
C |
4: 58,123,192 (GRCm39) |
D708G |
possibly damaging |
Het |
Taar6 |
T |
C |
10: 23,861,021 (GRCm39) |
D175G |
probably benign |
Het |
Thbs1 |
A |
C |
2: 117,953,358 (GRCm39) |
D925A |
probably damaging |
Het |
Tnr |
A |
T |
1: 159,714,595 (GRCm39) |
T825S |
probably benign |
Het |
Ttc23l |
A |
C |
15: 10,551,627 (GRCm39) |
L33W |
probably damaging |
Het |
Ttc39d |
T |
C |
17: 80,523,379 (GRCm39) |
Y13H |
probably benign |
Het |
Vmn2r102 |
C |
A |
17: 19,880,851 (GRCm39) |
P64Q |
probably damaging |
Het |
Vps11 |
G |
T |
9: 44,267,588 (GRCm39) |
Y341* |
probably null |
Het |
Vsig8 |
T |
C |
1: 172,387,925 (GRCm39) |
V5A |
possibly damaging |
Het |
Vwce |
C |
T |
19: 10,624,177 (GRCm39) |
A356V |
probably benign |
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 |
IGL01845:Abca1
|
APN |
4 |
53,090,297 (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 |
|
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 |
|