Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3425401B19Rik |
A |
G |
14: 32,384,588 (GRCm39) |
V459A |
probably benign |
Het |
Abhd6 |
T |
G |
14: 8,039,771 (GRCm38) |
M1R |
probably null |
Het |
Abl1 |
T |
C |
2: 31,690,254 (GRCm39) |
L572P |
probably damaging |
Het |
Adamts2 |
C |
A |
11: 50,694,517 (GRCm39) |
S1101R |
probably benign |
Het |
Adgra2 |
G |
A |
8: 27,600,507 (GRCm39) |
W200* |
probably null |
Het |
AI661453 |
C |
A |
17: 47,778,112 (GRCm39) |
|
probably benign |
Het |
Aldh1l2 |
A |
G |
10: 83,342,496 (GRCm39) |
F438S |
probably damaging |
Het |
Ankrd49 |
G |
A |
9: 14,692,510 (GRCm39) |
T218I |
possibly damaging |
Het |
Ano7 |
T |
C |
1: 93,322,288 (GRCm39) |
F410L |
probably benign |
Het |
Aox4 |
T |
A |
1: 58,305,808 (GRCm39) |
F1271I |
probably damaging |
Het |
Aqr |
T |
C |
2: 114,005,695 (GRCm39) |
|
probably benign |
Het |
Arhgap42 |
A |
G |
9: 9,180,118 (GRCm39) |
S54P |
probably damaging |
Het |
Aunip |
C |
A |
4: 134,238,450 (GRCm39) |
D16E |
possibly damaging |
Het |
Btbd7 |
A |
G |
12: 102,760,003 (GRCm39) |
|
probably null |
Het |
Cabp4 |
T |
C |
19: 4,189,290 (GRCm39) |
H89R |
probably benign |
Het |
Ccni |
AAA |
AAACTAA |
5: 93,335,429 (GRCm39) |
|
probably benign |
Het |
Chfr |
C |
T |
5: 110,306,700 (GRCm39) |
H410Y |
probably damaging |
Het |
Churc1 |
C |
A |
12: 76,829,671 (GRCm39) |
L111M |
probably damaging |
Het |
Clasp1 |
C |
T |
1: 118,388,980 (GRCm39) |
T113I |
probably benign |
Het |
Col12a1 |
T |
A |
9: 79,600,849 (GRCm39) |
Q745L |
probably benign |
Het |
Col20a1 |
T |
C |
2: 180,640,454 (GRCm39) |
L537P |
probably damaging |
Het |
Creb5 |
A |
T |
6: 53,587,411 (GRCm39) |
E47V |
probably null |
Het |
Csnk1d |
A |
T |
11: 120,854,668 (GRCm39) |
|
probably benign |
Het |
Cts6 |
A |
T |
13: 61,349,995 (GRCm39) |
W29R |
probably damaging |
Het |
Dbt |
T |
A |
3: 116,339,992 (GRCm39) |
I420N |
probably damaging |
Het |
Det1 |
C |
A |
7: 78,493,555 (GRCm39) |
D150Y |
probably damaging |
Het |
Dlk2 |
A |
G |
17: 46,609,940 (GRCm39) |
|
probably null |
Het |
Dnmt3a |
A |
T |
12: 3,950,352 (GRCm39) |
I639F |
probably damaging |
Het |
Dock9 |
A |
T |
14: 121,784,008 (GRCm39) |
Y1989N |
probably benign |
Het |
Dsg4 |
A |
T |
18: 20,599,678 (GRCm39) |
T765S |
possibly damaging |
Het |
Entrep2 |
G |
A |
7: 64,426,488 (GRCm39) |
T159I |
probably damaging |
Het |
Epha5 |
C |
T |
5: 84,253,750 (GRCm39) |
D548N |
possibly damaging |
Het |
Fam227b |
T |
A |
2: 125,958,045 (GRCm39) |
Y240F |
possibly damaging |
Het |
Fbxw21 |
C |
T |
9: 108,972,458 (GRCm39) |
V395I |
probably damaging |
Het |
Fn1 |
C |
A |
1: 71,691,959 (GRCm39) |
|
probably benign |
Het |
Fpr-rs3 |
A |
T |
17: 20,844,683 (GRCm39) |
S153T |
probably benign |
Het |
Frem2 |
A |
G |
3: 53,561,316 (GRCm39) |
F1064L |
probably benign |
Het |
Gas2l3 |
CACTCGTCATACT |
CACT |
10: 89,266,820 (GRCm39) |
|
probably benign |
Het |
Gjd2 |
C |
T |
2: 113,842,022 (GRCm39) |
G152R |
probably damaging |
Het |
Gpr75 |
T |
C |
11: 30,842,154 (GRCm39) |
I353T |
possibly damaging |
Het |
Grb7 |
T |
C |
11: 98,342,262 (GRCm39) |
V145A |
possibly damaging |
Het |
Igkv4-73 |
G |
A |
6: 69,174,807 (GRCm39) |
R40W |
unknown |
Het |
Kif1c |
C |
T |
11: 70,617,183 (GRCm39) |
A839V |
probably benign |
Het |
Krt31 |
G |
A |
11: 99,940,748 (GRCm39) |
A125V |
possibly damaging |
Het |
Lamb1 |
A |
G |
12: 31,328,525 (GRCm39) |
Y163C |
probably damaging |
Het |
Mars1 |
G |
T |
10: 127,136,084 (GRCm39) |
T535K |
probably damaging |
Het |
Mdc1 |
T |
C |
17: 36,159,993 (GRCm39) |
|
probably null |
Het |
Micos10 |
C |
G |
4: 138,858,268 (GRCm39) |
W10S |
probably damaging |
Het |
Micu1 |
C |
T |
10: 59,576,644 (GRCm39) |
H167Y |
probably benign |
Het |
Mrgprb1 |
C |
T |
7: 48,097,739 (GRCm39) |
V58I |
possibly damaging |
Het |
Ncoa7 |
T |
A |
10: 30,647,758 (GRCm39) |
E6V |
possibly damaging |
Het |
Nectin3 |
A |
C |
16: 46,268,523 (GRCm39) |
|
probably benign |
Het |
Or13a18 |
A |
G |
7: 140,190,987 (GRCm39) |
K295E |
probably damaging |
Het |
Or4k44 |
C |
T |
2: 111,367,956 (GRCm39) |
C226Y |
probably benign |
Het |
Or52ab7 |
T |
A |
7: 102,977,730 (GRCm39) |
Y12* |
probably null |
Het |
Or8k38 |
T |
A |
2: 86,488,029 (GRCm39) |
M258L |
possibly damaging |
Het |
Pex16 |
T |
C |
2: 92,206,983 (GRCm39) |
S54P |
probably damaging |
Het |
Pik3cg |
A |
T |
12: 32,254,080 (GRCm39) |
S636T |
possibly damaging |
Het |
Plin5 |
A |
G |
17: 56,423,855 (GRCm39) |
S27P |
probably benign |
Het |
Ptch1 |
A |
T |
13: 63,661,522 (GRCm39) |
D1068E |
probably damaging |
Het |
Ptprq |
T |
C |
10: 107,399,036 (GRCm39) |
T1960A |
probably damaging |
Het |
Rap1gap2 |
T |
C |
11: 74,298,800 (GRCm39) |
|
probably benign |
Het |
Rcc2 |
G |
A |
4: 140,444,353 (GRCm39) |
R348Q |
probably damaging |
Het |
Rhbdd3 |
C |
A |
11: 5,055,949 (GRCm39) |
A377D |
probably damaging |
Het |
Rpl7 |
T |
G |
1: 16,172,189 (GRCm39) |
|
probably benign |
Het |
Scn11a |
G |
T |
9: 119,648,936 (GRCm39) |
D42E |
probably benign |
Het |
Scube3 |
C |
T |
17: 28,384,147 (GRCm39) |
R549W |
probably damaging |
Het |
Sil1 |
A |
T |
18: 35,458,428 (GRCm39) |
M189K |
probably damaging |
Het |
Slc39a6 |
G |
A |
18: 24,718,531 (GRCm39) |
Q225* |
probably null |
Het |
Slc7a15 |
A |
T |
12: 8,589,002 (GRCm39) |
C182S |
probably benign |
Het |
Spata21 |
G |
A |
4: 140,824,431 (GRCm39) |
|
probably null |
Het |
Stim2 |
T |
C |
5: 54,267,955 (GRCm39) |
V417A |
probably damaging |
Het |
Szt2 |
T |
C |
4: 118,246,182 (GRCm39) |
D993G |
probably damaging |
Het |
Tet3 |
A |
G |
6: 83,379,928 (GRCm39) |
S747P |
probably benign |
Het |
Tmem86a |
C |
G |
7: 46,702,678 (GRCm39) |
S34R |
possibly damaging |
Het |
Top2b |
T |
A |
14: 16,383,125 (GRCm38) |
S38T |
probably benign |
Het |
Trim33 |
A |
T |
3: 103,236,572 (GRCm39) |
T561S |
possibly damaging |
Het |
Ttc39a |
C |
T |
4: 109,273,218 (GRCm39) |
Q25* |
probably null |
Het |
Urb1 |
A |
G |
16: 90,556,730 (GRCm39) |
I1816T |
possibly damaging |
Het |
Usp24 |
T |
C |
4: 106,270,873 (GRCm39) |
|
probably null |
Het |
Usp36 |
A |
C |
11: 118,153,896 (GRCm39) |
L840R |
probably damaging |
Het |
Usp50 |
C |
A |
2: 126,619,773 (GRCm39) |
|
probably benign |
Het |
Vangl2 |
A |
G |
1: 171,837,230 (GRCm39) |
V193A |
possibly damaging |
Het |
Vmn1r62 |
T |
A |
7: 5,678,866 (GRCm39) |
H182Q |
probably benign |
Het |
Vmn2r124 |
A |
T |
17: 18,294,007 (GRCm39) |
Y698F |
probably benign |
Het |
Wls |
C |
T |
3: 159,603,082 (GRCm39) |
T165I |
probably benign |
Het |
Zfp808 |
G |
T |
13: 62,319,106 (GRCm39) |
E112* |
probably null |
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 |
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 |
R6999:Abca12
|
UTSW |
1 |
71,356,321 (GRCm39) |
nonsense |
probably null |
|
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 |
|