Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acss3 |
C |
A |
10: 106,889,362 (GRCm39) |
G153C |
probably damaging |
Het |
Alpk2 |
A |
G |
18: 65,437,584 (GRCm39) |
S1270P |
probably damaging |
Het |
Ankrd10 |
A |
T |
8: 11,669,106 (GRCm39) |
L215Q |
probably damaging |
Het |
Ankrd6 |
A |
G |
4: 32,823,459 (GRCm39) |
S188P |
probably benign |
Het |
Brinp2 |
A |
G |
1: 158,078,875 (GRCm39) |
M316T |
probably benign |
Het |
Bsn |
A |
G |
9: 107,990,632 (GRCm39) |
S1707P |
probably benign |
Het |
C2cd4b |
C |
T |
9: 67,667,571 (GRCm39) |
A189V |
probably benign |
Het |
Camk2b |
C |
T |
11: 5,922,321 (GRCm39) |
R556H |
probably damaging |
Het |
Cfap126 |
A |
G |
1: 170,953,733 (GRCm39) |
D101G |
possibly damaging |
Het |
Chd5 |
A |
T |
4: 152,458,891 (GRCm39) |
I1085F |
probably damaging |
Het |
Chp2 |
A |
G |
7: 121,821,092 (GRCm39) |
E151G |
probably damaging |
Het |
Chrd |
A |
G |
16: 20,554,402 (GRCm39) |
T370A |
probably benign |
Het |
Chrnb2 |
C |
T |
3: 89,668,622 (GRCm39) |
R231H |
possibly damaging |
Het |
Crisp4 |
T |
A |
1: 18,207,259 (GRCm39) |
I10F |
possibly damaging |
Het |
Csnka2ip |
T |
A |
16: 64,298,933 (GRCm39) |
H477L |
unknown |
Het |
Ctu1 |
T |
A |
7: 43,324,662 (GRCm39) |
F34I |
probably damaging |
Het |
Dctn1 |
T |
A |
6: 83,168,263 (GRCm39) |
S407T |
possibly damaging |
Het |
Ech1 |
T |
C |
7: 28,529,689 (GRCm39) |
F191L |
probably benign |
Het |
Enpp3 |
T |
C |
10: 24,684,064 (GRCm39) |
D60G |
probably damaging |
Het |
Epha6 |
T |
C |
16: 60,245,533 (GRCm39) |
Y222C |
possibly damaging |
Het |
Eppk1 |
A |
T |
15: 75,993,423 (GRCm39) |
W1153R |
probably benign |
Het |
Fbxo4 |
C |
T |
15: 4,007,437 (GRCm39) |
D76N |
probably damaging |
Het |
Fndc7 |
G |
A |
3: 108,783,964 (GRCm39) |
A215V |
probably benign |
Het |
Gemin5 |
C |
T |
11: 58,015,947 (GRCm39) |
R1352Q |
probably benign |
Het |
Gm9639 |
T |
C |
10: 77,630,525 (GRCm39) |
|
probably benign |
Het |
Gm973 |
C |
A |
1: 59,673,251 (GRCm39) |
Q160K |
unknown |
Het |
Gpatch2l |
G |
A |
12: 86,290,958 (GRCm39) |
R47H |
probably damaging |
Het |
Grid2 |
A |
T |
6: 64,053,893 (GRCm39) |
Q364L |
possibly damaging |
Het |
Kcnn2 |
T |
G |
18: 45,725,444 (GRCm39) |
S313R |
probably damaging |
Het |
Kera |
T |
C |
10: 97,444,814 (GRCm39) |
Y58H |
probably damaging |
Het |
Meiosin |
A |
G |
7: 18,836,300 (GRCm39) |
|
probably benign |
Het |
Mtfr2 |
T |
C |
10: 20,229,862 (GRCm39) |
L105P |
probably benign |
Het |
Myom2 |
A |
G |
8: 15,134,531 (GRCm39) |
T445A |
probably benign |
Het |
Or2o1 |
A |
G |
11: 49,051,239 (GRCm39) |
R133G |
possibly damaging |
Het |
Or8b1c |
T |
A |
9: 38,384,535 (GRCm39) |
L164Q |
probably damaging |
Het |
Pcdha12 |
T |
C |
18: 37,153,329 (GRCm39) |
L16P |
probably benign |
Het |
Pcdhb10 |
T |
C |
18: 37,546,171 (GRCm39) |
Y416H |
probably damaging |
Het |
Pde8b |
T |
C |
13: 95,223,342 (GRCm39) |
Y304C |
possibly damaging |
Het |
Pkd1 |
T |
C |
17: 24,797,475 (GRCm39) |
I2605T |
possibly damaging |
Het |
Pnn |
T |
C |
12: 59,117,085 (GRCm39) |
|
probably null |
Het |
Ppa1 |
G |
A |
10: 61,496,796 (GRCm39) |
G95S |
probably damaging |
Het |
Rapgef4 |
G |
T |
2: 72,069,469 (GRCm39) |
A730S |
probably damaging |
Het |
Scap |
A |
G |
9: 110,213,715 (GRCm39) |
Y1226C |
probably damaging |
Het |
Scn2a |
A |
T |
2: 65,512,453 (GRCm39) |
T197S |
probably benign |
Het |
Slc2a6 |
GCTTCC |
GC |
2: 26,916,047 (GRCm39) |
|
probably null |
Het |
Slc8a3 |
T |
C |
12: 81,361,529 (GRCm39) |
Y430C |
probably benign |
Het |
Tead3 |
T |
C |
17: 28,560,506 (GRCm39) |
T33A |
probably benign |
Het |
Tep1 |
T |
A |
14: 51,088,162 (GRCm39) |
I792F |
possibly damaging |
Het |
Trpm2 |
A |
T |
10: 77,771,725 (GRCm39) |
I638N |
probably damaging |
Het |
Tuba1c |
A |
G |
15: 98,935,193 (GRCm39) |
D218G |
probably benign |
Het |
Tubgcp4 |
T |
A |
2: 121,022,778 (GRCm39) |
W495R |
probably damaging |
Het |
Tut1 |
T |
C |
19: 8,943,382 (GRCm39) |
L823P |
probably damaging |
Het |
Ube2q2l |
T |
C |
6: 136,378,272 (GRCm39) |
N186S |
probably benign |
Het |
Umodl1 |
C |
T |
17: 31,218,097 (GRCm39) |
A1228V |
probably damaging |
Het |
Vmn1r235 |
T |
A |
17: 21,482,127 (GRCm39) |
F151I |
probably benign |
Het |
Vmn2r45 |
T |
A |
7: 8,486,219 (GRCm39) |
K356N |
probably benign |
Het |
Zfp318 |
T |
A |
17: 46,710,969 (GRCm39) |
N897K |
probably damaging |
Het |
|
Other mutations in Abca12 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00089:Abca12
|
APN |
1 |
71,342,700 (GRCm39) |
missense |
possibly damaging |
0.64 |
IGL00556:Abca12
|
APN |
1 |
71,392,916 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00813:Abca12
|
APN |
1 |
71,392,921 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL00835:Abca12
|
APN |
1 |
71,341,892 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00921:Abca12
|
APN |
1 |
71,324,888 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01011:Abca12
|
APN |
1 |
71,302,791 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01066:Abca12
|
APN |
1 |
71,392,889 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01082:Abca12
|
APN |
1 |
71,353,273 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01310:Abca12
|
APN |
1 |
71,323,315 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01360:Abca12
|
APN |
1 |
71,325,648 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01585:Abca12
|
APN |
1 |
71,359,045 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01608:Abca12
|
APN |
1 |
71,298,601 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01687:Abca12
|
APN |
1 |
71,306,769 (GRCm39) |
splice site |
probably benign |
|
IGL01700:Abca12
|
APN |
1 |
71,319,549 (GRCm39) |
missense |
probably benign |
|
IGL01723:Abca12
|
APN |
1 |
71,353,327 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01804:Abca12
|
APN |
1 |
71,315,342 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01982:Abca12
|
APN |
1 |
71,385,857 (GRCm39) |
missense |
probably benign |
0.34 |
IGL02136:Abca12
|
APN |
1 |
71,286,301 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02172:Abca12
|
APN |
1 |
71,341,817 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02222:Abca12
|
APN |
1 |
71,322,045 (GRCm39) |
missense |
probably benign |
0.40 |
IGL02266:Abca12
|
APN |
1 |
71,307,360 (GRCm39) |
nonsense |
probably null |
|
IGL02449:Abca12
|
APN |
1 |
71,440,908 (GRCm39) |
splice site |
probably null |
|
IGL02471:Abca12
|
APN |
1 |
71,297,357 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02496:Abca12
|
APN |
1 |
71,327,712 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL02552:Abca12
|
APN |
1 |
71,333,906 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02795:Abca12
|
APN |
1 |
71,327,907 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03000:Abca12
|
APN |
1 |
71,360,959 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03031:Abca12
|
APN |
1 |
71,353,183 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03131:Abca12
|
APN |
1 |
71,385,861 (GRCm39) |
missense |
probably benign |
|
IGL03260:Abca12
|
APN |
1 |
71,323,258 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03324:Abca12
|
APN |
1 |
71,353,167 (GRCm39) |
missense |
probably benign |
|
IGL03408:Abca12
|
APN |
1 |
71,303,954 (GRCm39) |
missense |
probably damaging |
1.00 |
R0016:Abca12
|
UTSW |
1 |
71,333,959 (GRCm39) |
missense |
probably benign |
0.35 |
R0016:Abca12
|
UTSW |
1 |
71,333,959 (GRCm39) |
missense |
probably benign |
0.35 |
R0121:Abca12
|
UTSW |
1 |
71,298,945 (GRCm39) |
splice site |
probably null |
|
R0172:Abca12
|
UTSW |
1 |
71,318,561 (GRCm39) |
missense |
probably damaging |
0.99 |
R0196:Abca12
|
UTSW |
1 |
71,298,972 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0400:Abca12
|
UTSW |
1 |
71,298,935 (GRCm39) |
splice site |
probably benign |
|
R0466:Abca12
|
UTSW |
1 |
71,341,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R0616:Abca12
|
UTSW |
1 |
71,341,830 (GRCm39) |
missense |
probably damaging |
1.00 |
R0668:Abca12
|
UTSW |
1 |
71,302,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R0928:Abca12
|
UTSW |
1 |
71,388,333 (GRCm39) |
missense |
probably benign |
0.06 |
R1036:Abca12
|
UTSW |
1 |
71,302,569 (GRCm39) |
critical splice donor site |
probably null |
|
R1086:Abca12
|
UTSW |
1 |
71,334,220 (GRCm39) |
splice site |
probably benign |
|
R1300:Abca12
|
UTSW |
1 |
71,283,967 (GRCm39) |
missense |
probably damaging |
1.00 |
R1337:Abca12
|
UTSW |
1 |
71,333,978 (GRCm39) |
missense |
probably benign |
0.03 |
R1356:Abca12
|
UTSW |
1 |
71,342,112 (GRCm39) |
splice site |
probably benign |
|
R1372:Abca12
|
UTSW |
1 |
71,334,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R1434:Abca12
|
UTSW |
1 |
71,348,959 (GRCm39) |
missense |
probably benign |
0.00 |
R1580:Abca12
|
UTSW |
1 |
71,305,124 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1675:Abca12
|
UTSW |
1 |
71,302,570 (GRCm39) |
critical splice donor site |
probably null |
|
R1773:Abca12
|
UTSW |
1 |
71,327,755 (GRCm39) |
missense |
probably damaging |
1.00 |
R1829:Abca12
|
UTSW |
1 |
71,334,188 (GRCm39) |
missense |
probably benign |
0.26 |
R1922:Abca12
|
UTSW |
1 |
71,359,083 (GRCm39) |
missense |
probably benign |
0.10 |
R1927:Abca12
|
UTSW |
1 |
71,283,999 (GRCm39) |
missense |
probably damaging |
1.00 |
R2115:Abca12
|
UTSW |
1 |
71,283,930 (GRCm39) |
missense |
probably benign |
0.01 |
R2146:Abca12
|
UTSW |
1 |
71,302,647 (GRCm39) |
missense |
probably benign |
0.02 |
R2148:Abca12
|
UTSW |
1 |
71,302,647 (GRCm39) |
missense |
probably benign |
0.02 |
R2149:Abca12
|
UTSW |
1 |
71,302,647 (GRCm39) |
missense |
probably benign |
0.02 |
R2150:Abca12
|
UTSW |
1 |
71,302,647 (GRCm39) |
missense |
probably benign |
0.02 |
R2299:Abca12
|
UTSW |
1 |
71,297,381 (GRCm39) |
missense |
probably damaging |
1.00 |
R2392:Abca12
|
UTSW |
1 |
71,297,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R2571:Abca12
|
UTSW |
1 |
71,289,044 (GRCm39) |
missense |
probably benign |
0.00 |
R3077:Abca12
|
UTSW |
1 |
71,306,764 (GRCm39) |
missense |
probably benign |
0.02 |
R3078:Abca12
|
UTSW |
1 |
71,306,764 (GRCm39) |
missense |
probably benign |
0.02 |
R3705:Abca12
|
UTSW |
1 |
71,324,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R3800:Abca12
|
UTSW |
1 |
71,305,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R3905:Abca12
|
UTSW |
1 |
71,318,616 (GRCm39) |
missense |
probably benign |
0.02 |
R3905:Abca12
|
UTSW |
1 |
71,307,389 (GRCm39) |
missense |
possibly damaging |
0.79 |
R3962:Abca12
|
UTSW |
1 |
71,313,674 (GRCm39) |
splice site |
probably null |
|
R4082:Abca12
|
UTSW |
1 |
71,306,622 (GRCm39) |
missense |
possibly damaging |
0.64 |
R4131:Abca12
|
UTSW |
1 |
71,359,030 (GRCm39) |
critical splice donor site |
probably null |
|
R4214:Abca12
|
UTSW |
1 |
71,327,856 (GRCm39) |
missense |
probably damaging |
0.99 |
R4403:Abca12
|
UTSW |
1 |
71,306,595 (GRCm39) |
missense |
probably damaging |
1.00 |
R4524:Abca12
|
UTSW |
1 |
71,342,076 (GRCm39) |
missense |
probably benign |
0.19 |
R4615:Abca12
|
UTSW |
1 |
71,369,493 (GRCm39) |
missense |
probably benign |
|
R4617:Abca12
|
UTSW |
1 |
71,369,493 (GRCm39) |
missense |
probably benign |
|
R4714:Abca12
|
UTSW |
1 |
71,360,609 (GRCm39) |
missense |
probably benign |
0.00 |
R4809:Abca12
|
UTSW |
1 |
71,318,015 (GRCm39) |
missense |
probably benign |
0.10 |
R4810:Abca12
|
UTSW |
1 |
71,342,771 (GRCm39) |
missense |
probably benign |
0.00 |
R4825:Abca12
|
UTSW |
1 |
71,341,844 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4990:Abca12
|
UTSW |
1 |
71,334,098 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5013:Abca12
|
UTSW |
1 |
71,303,926 (GRCm39) |
missense |
probably damaging |
0.99 |
R5026:Abca12
|
UTSW |
1 |
71,356,383 (GRCm39) |
missense |
probably benign |
0.04 |
R5064:Abca12
|
UTSW |
1 |
71,340,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R5188:Abca12
|
UTSW |
1 |
71,330,651 (GRCm39) |
missense |
probably benign |
0.23 |
R5234:Abca12
|
UTSW |
1 |
71,302,823 (GRCm39) |
missense |
probably damaging |
0.99 |
R5267:Abca12
|
UTSW |
1 |
71,374,933 (GRCm39) |
splice site |
probably benign |
|
R5302:Abca12
|
UTSW |
1 |
71,323,111 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5441:Abca12
|
UTSW |
1 |
71,334,215 (GRCm39) |
missense |
probably damaging |
1.00 |
R5451:Abca12
|
UTSW |
1 |
71,334,076 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5526:Abca12
|
UTSW |
1 |
71,331,605 (GRCm39) |
missense |
probably benign |
0.29 |
R5529:Abca12
|
UTSW |
1 |
71,304,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R5615:Abca12
|
UTSW |
1 |
71,346,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R5649:Abca12
|
UTSW |
1 |
71,330,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R5800:Abca12
|
UTSW |
1 |
71,360,591 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5807:Abca12
|
UTSW |
1 |
71,342,651 (GRCm39) |
missense |
probably damaging |
1.00 |
R5878:Abca12
|
UTSW |
1 |
71,385,792 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5987:Abca12
|
UTSW |
1 |
71,297,257 (GRCm39) |
missense |
probably damaging |
1.00 |
R6280:Abca12
|
UTSW |
1 |
71,311,619 (GRCm39) |
missense |
probably benign |
0.04 |
R6316:Abca12
|
UTSW |
1 |
71,353,118 (GRCm39) |
missense |
probably benign |
0.01 |
R6337:Abca12
|
UTSW |
1 |
71,334,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R6383:Abca12
|
UTSW |
1 |
71,286,343 (GRCm39) |
missense |
probably benign |
0.03 |
R6564:Abca12
|
UTSW |
1 |
71,349,009 (GRCm39) |
missense |
possibly damaging |
0.57 |
R6582:Abca12
|
UTSW |
1 |
71,297,384 (GRCm39) |
missense |
probably benign |
0.00 |
R6756:Abca12
|
UTSW |
1 |
71,298,512 (GRCm39) |
splice site |
probably null |
|
R6876:Abca12
|
UTSW |
1 |
71,302,667 (GRCm39) |
missense |
probably damaging |
0.98 |
R7145:Abca12
|
UTSW |
1 |
71,346,212 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7272:Abca12
|
UTSW |
1 |
71,287,591 (GRCm39) |
missense |
probably damaging |
0.99 |
R7285:Abca12
|
UTSW |
1 |
71,388,314 (GRCm39) |
nonsense |
probably null |
|
R7421:Abca12
|
UTSW |
1 |
71,286,295 (GRCm39) |
nonsense |
probably null |
|
R7531:Abca12
|
UTSW |
1 |
71,286,332 (GRCm39) |
missense |
probably damaging |
0.99 |
R7592:Abca12
|
UTSW |
1 |
71,327,836 (GRCm39) |
missense |
probably benign |
0.01 |
R7687:Abca12
|
UTSW |
1 |
71,297,341 (GRCm39) |
missense |
probably benign |
0.00 |
R7690:Abca12
|
UTSW |
1 |
71,353,313 (GRCm39) |
missense |
probably benign |
0.00 |
R7709:Abca12
|
UTSW |
1 |
71,374,887 (GRCm39) |
missense |
probably benign |
0.00 |
R7736:Abca12
|
UTSW |
1 |
71,359,123 (GRCm39) |
missense |
probably benign |
0.01 |
R7754:Abca12
|
UTSW |
1 |
71,342,046 (GRCm39) |
missense |
probably benign |
|
R7761:Abca12
|
UTSW |
1 |
71,369,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R7808:Abca12
|
UTSW |
1 |
71,313,793 (GRCm39) |
splice site |
probably null |
|
R7816:Abca12
|
UTSW |
1 |
71,331,588 (GRCm39) |
missense |
probably benign |
0.01 |
R7821:Abca12
|
UTSW |
1 |
71,298,950 (GRCm39) |
missense |
probably benign |
0.12 |
R7827:Abca12
|
UTSW |
1 |
71,453,837 (GRCm39) |
start gained |
probably benign |
|
R7829:Abca12
|
UTSW |
1 |
71,331,580 (GRCm39) |
missense |
probably benign |
0.37 |
R7863:Abca12
|
UTSW |
1 |
71,332,656 (GRCm39) |
missense |
probably damaging |
0.96 |
R8053:Abca12
|
UTSW |
1 |
71,388,328 (GRCm39) |
nonsense |
probably null |
|
R8093:Abca12
|
UTSW |
1 |
71,319,552 (GRCm39) |
missense |
probably benign |
0.00 |
R8120:Abca12
|
UTSW |
1 |
71,298,540 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8136:Abca12
|
UTSW |
1 |
71,287,556 (GRCm39) |
missense |
probably benign |
0.15 |
R8155:Abca12
|
UTSW |
1 |
71,330,497 (GRCm39) |
missense |
probably damaging |
1.00 |
R8189:Abca12
|
UTSW |
1 |
71,324,885 (GRCm39) |
missense |
probably damaging |
1.00 |
R8233:Abca12
|
UTSW |
1 |
71,390,916 (GRCm39) |
missense |
probably benign |
0.00 |
R8249:Abca12
|
UTSW |
1 |
71,360,971 (GRCm39) |
missense |
probably benign |
0.00 |
R8255:Abca12
|
UTSW |
1 |
71,359,058 (GRCm39) |
missense |
probably benign |
0.13 |
R8300:Abca12
|
UTSW |
1 |
71,353,123 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8339:Abca12
|
UTSW |
1 |
71,324,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R8490:Abca12
|
UTSW |
1 |
71,323,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R8494:Abca12
|
UTSW |
1 |
71,327,821 (GRCm39) |
missense |
probably benign |
0.02 |
R8527:Abca12
|
UTSW |
1 |
71,349,047 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8542:Abca12
|
UTSW |
1 |
71,349,047 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8692:Abca12
|
UTSW |
1 |
71,327,874 (GRCm39) |
missense |
probably damaging |
0.96 |
R8723:Abca12
|
UTSW |
1 |
71,360,897 (GRCm39) |
missense |
probably benign |
0.04 |
R8796:Abca12
|
UTSW |
1 |
71,297,248 (GRCm39) |
critical splice donor site |
probably benign |
|
R8911:Abca12
|
UTSW |
1 |
71,380,690 (GRCm39) |
missense |
probably benign |
0.07 |
R8913:Abca12
|
UTSW |
1 |
71,303,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R8957:Abca12
|
UTSW |
1 |
71,360,784 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9000:Abca12
|
UTSW |
1 |
71,353,195 (GRCm39) |
missense |
probably damaging |
1.00 |
R9137:Abca12
|
UTSW |
1 |
71,298,525 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9228:Abca12
|
UTSW |
1 |
71,332,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R9237:Abca12
|
UTSW |
1 |
71,318,557 (GRCm39) |
missense |
probably damaging |
0.97 |
R9299:Abca12
|
UTSW |
1 |
71,359,042 (GRCm39) |
missense |
possibly damaging |
0.48 |
R9419:Abca12
|
UTSW |
1 |
71,342,649 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9492:Abca12
|
UTSW |
1 |
71,297,380 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9538:Abca12
|
UTSW |
1 |
71,380,672 (GRCm39) |
missense |
probably benign |
0.04 |
R9585:Abca12
|
UTSW |
1 |
71,342,745 (GRCm39) |
missense |
probably damaging |
1.00 |
R9658:Abca12
|
UTSW |
1 |
71,325,634 (GRCm39) |
missense |
probably damaging |
0.97 |
R9763:Abca12
|
UTSW |
1 |
71,302,717 (GRCm39) |
missense |
possibly damaging |
0.84 |
X0013:Abca12
|
UTSW |
1 |
71,287,592 (GRCm39) |
missense |
probably damaging |
0.99 |
X0018:Abca12
|
UTSW |
1 |
71,353,669 (GRCm39) |
missense |
probably benign |
|
X0063:Abca12
|
UTSW |
1 |
71,388,223 (GRCm39) |
missense |
probably benign |
0.15 |
X0065:Abca12
|
UTSW |
1 |
71,380,620 (GRCm39) |
critical splice donor site |
probably null |
|
Z1176:Abca12
|
UTSW |
1 |
71,323,229 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Abca12
|
UTSW |
1 |
71,331,690 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1177:Abca12
|
UTSW |
1 |
71,321,970 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1177:Abca12
|
UTSW |
1 |
71,315,241 (GRCm39) |
missense |
possibly damaging |
0.94 |
|