Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700113H08Rik |
T |
C |
10: 86,957,297 (GRCm39) |
V11A |
probably benign |
Het |
Abcc12 |
T |
A |
8: 87,234,568 (GRCm39) |
M1232L |
probably benign |
Het |
Adamts1 |
T |
C |
16: 85,597,117 (GRCm39) |
Y314C |
probably damaging |
Het |
Adgb |
A |
G |
10: 10,254,403 (GRCm39) |
|
probably null |
Het |
Ankrd12 |
T |
A |
17: 66,292,648 (GRCm39) |
K928N |
possibly damaging |
Het |
Ano5 |
A |
T |
7: 51,237,543 (GRCm39) |
K789I |
possibly damaging |
Het |
Cacna1d |
G |
T |
14: 29,833,026 (GRCm39) |
N938K |
probably damaging |
Het |
Camk1g |
T |
C |
1: 193,032,593 (GRCm39) |
R273G |
possibly damaging |
Het |
Caprin2 |
C |
A |
6: 148,744,528 (GRCm39) |
V966F |
probably damaging |
Het |
Card6 |
T |
C |
15: 5,128,954 (GRCm39) |
H814R |
probably benign |
Het |
Cenatac |
T |
C |
9: 44,324,215 (GRCm39) |
Q228R |
probably null |
Het |
Cflar |
A |
G |
1: 58,750,740 (GRCm39) |
|
probably benign |
Het |
Cftr |
T |
A |
6: 18,204,204 (GRCm39) |
N66K |
probably benign |
Het |
Clasrp |
C |
T |
7: 19,322,671 (GRCm39) |
|
probably null |
Het |
Clec4a4 |
T |
C |
6: 122,967,339 (GRCm39) |
I5T |
probably damaging |
Het |
Cmtr2 |
T |
C |
8: 110,948,251 (GRCm39) |
I187T |
possibly damaging |
Het |
Cnga1 |
A |
T |
5: 72,761,616 (GRCm39) |
F633I |
possibly damaging |
Het |
Col16a1 |
C |
T |
4: 129,967,057 (GRCm39) |
P909S |
unknown |
Het |
Csf1 |
C |
A |
3: 107,667,361 (GRCm39) |
A7S |
possibly damaging |
Het |
Cstpp1 |
T |
C |
2: 91,274,939 (GRCm39) |
|
probably benign |
Het |
Dhx30 |
A |
T |
9: 109,915,270 (GRCm39) |
V833D |
probably benign |
Het |
Dlg2 |
T |
G |
7: 92,080,263 (GRCm39) |
I712M |
probably benign |
Het |
Dmxl1 |
T |
A |
18: 50,011,382 (GRCm39) |
F1180I |
probably benign |
Het |
Dnah9 |
T |
A |
11: 65,896,631 (GRCm39) |
K2398* |
probably null |
Het |
Dus1l |
C |
T |
11: 120,680,262 (GRCm39) |
G471D |
possibly damaging |
Het |
Dync1h1 |
A |
T |
12: 110,621,893 (GRCm39) |
N3412I |
possibly damaging |
Het |
Dync1i2 |
T |
A |
2: 71,081,178 (GRCm39) |
|
probably null |
Het |
Dysf |
T |
C |
6: 84,047,911 (GRCm39) |
S333P |
possibly damaging |
Het |
Eed |
A |
T |
7: 89,605,541 (GRCm39) |
N349K |
probably benign |
Het |
Eipr1 |
A |
T |
12: 28,816,769 (GRCm39) |
|
probably null |
Het |
Fbxw16 |
A |
C |
9: 109,277,222 (GRCm39) |
V40G |
probably damaging |
Het |
Fgfr4 |
A |
C |
13: 55,308,969 (GRCm39) |
R363S |
possibly damaging |
Het |
Fgl2 |
A |
T |
5: 21,578,229 (GRCm39) |
N172I |
possibly damaging |
Het |
Fhip1b |
G |
A |
7: 105,033,732 (GRCm39) |
R509C |
probably damaging |
Het |
Gabbr2 |
T |
A |
4: 46,875,744 (GRCm39) |
H126L |
possibly damaging |
Het |
Gcnt2 |
A |
T |
13: 41,014,338 (GRCm39) |
N170Y |
possibly damaging |
Het |
Gpt |
A |
G |
15: 76,583,093 (GRCm39) |
|
probably null |
Het |
Igsf10 |
A |
G |
3: 59,235,489 (GRCm39) |
I1564T |
probably benign |
Het |
Il22ra1 |
C |
A |
4: 135,478,107 (GRCm39) |
Q393K |
possibly damaging |
Het |
Inpp5d |
A |
T |
1: 87,611,567 (GRCm39) |
K340* |
probably null |
Het |
Jcad |
A |
G |
18: 4,673,113 (GRCm39) |
K292E |
probably damaging |
Het |
Krt5 |
T |
A |
15: 101,617,453 (GRCm39) |
T427S |
probably benign |
Het |
Krt76 |
T |
C |
15: 101,798,929 (GRCm39) |
D252G |
probably damaging |
Het |
Krtap26-1 |
A |
G |
16: 88,444,198 (GRCm39) |
V141A |
not run |
Het |
Lce6a |
A |
T |
3: 92,527,642 (GRCm39) |
V55D |
probably benign |
Het |
Lpxn |
C |
T |
19: 12,802,185 (GRCm39) |
S170F |
possibly damaging |
Het |
Magi2 |
T |
C |
5: 20,670,838 (GRCm39) |
V394A |
probably benign |
Het |
Mbnl1 |
G |
A |
3: 60,522,242 (GRCm39) |
|
probably null |
Het |
Med16 |
T |
A |
10: 79,734,252 (GRCm39) |
K554M |
probably damaging |
Het |
Mettl14 |
T |
C |
3: 123,166,234 (GRCm39) |
D276G |
possibly damaging |
Het |
Mphosph9 |
T |
C |
5: 124,399,009 (GRCm39) |
D1002G |
probably damaging |
Het |
Mroh9 |
T |
C |
1: 162,866,678 (GRCm39) |
E686G |
probably damaging |
Het |
Nav1 |
T |
C |
1: 135,379,986 (GRCm39) |
Y1512C |
unknown |
Het |
Neb |
T |
C |
2: 52,082,035 (GRCm39) |
Y5712C |
probably damaging |
Het |
Nek7 |
T |
A |
1: 138,489,509 (GRCm39) |
|
probably benign |
Het |
Nptx1 |
T |
A |
11: 119,435,462 (GRCm39) |
I285F |
probably damaging |
Het |
Oas1d |
G |
T |
5: 121,053,034 (GRCm39) |
E30* |
probably null |
Het |
Or1p1b |
A |
T |
11: 74,130,725 (GRCm39) |
I112F |
probably damaging |
Het |
Or51g2 |
A |
G |
7: 102,622,317 (GRCm39) |
V294A |
possibly damaging |
Het |
Or6n1 |
C |
A |
1: 173,917,417 (GRCm39) |
Y270* |
probably null |
Het |
Parp4 |
T |
G |
14: 56,873,205 (GRCm39) |
S1150A |
possibly damaging |
Het |
Pinx1 |
A |
T |
14: 64,156,741 (GRCm39) |
K223* |
probably null |
Het |
Plekha5 |
T |
C |
6: 140,529,640 (GRCm39) |
L1034S |
probably damaging |
Het |
Ppp4r3a |
A |
G |
12: 101,019,755 (GRCm39) |
V400A |
possibly damaging |
Het |
Prtg |
A |
T |
9: 72,749,979 (GRCm39) |
I128F |
possibly damaging |
Het |
Rars1 |
T |
C |
11: 35,719,534 (GRCm39) |
E96G |
probably benign |
Het |
Rhpn1 |
T |
A |
15: 75,585,299 (GRCm39) |
S551T |
probably benign |
Het |
Selenow |
C |
T |
7: 15,656,176 (GRCm39) |
|
probably null |
Het |
Serpina9 |
A |
T |
12: 103,967,484 (GRCm39) |
|
probably null |
Het |
Shank3 |
A |
T |
15: 89,433,083 (GRCm39) |
D1276V |
probably damaging |
Het |
Slc27a6 |
A |
G |
18: 58,742,267 (GRCm39) |
T494A |
probably damaging |
Het |
Slc34a1 |
A |
C |
13: 24,003,317 (GRCm39) |
H285P |
probably damaging |
Het |
Slc6a21 |
A |
C |
7: 44,932,360 (GRCm39) |
T54P |
|
Het |
Syne2 |
A |
G |
12: 76,030,501 (GRCm39) |
|
probably null |
Het |
Tal1 |
T |
C |
4: 114,925,489 (GRCm39) |
V186A |
probably benign |
Het |
Tars3 |
A |
G |
7: 65,302,009 (GRCm39) |
K178E |
probably benign |
Het |
Tex10 |
T |
A |
4: 48,459,984 (GRCm39) |
I456L |
probably benign |
Het |
Tfcp2 |
A |
G |
15: 100,420,310 (GRCm39) |
F175S |
probably damaging |
Het |
Timp2 |
C |
T |
11: 118,194,626 (GRCm39) |
A188T |
probably damaging |
Het |
Tmc5 |
T |
A |
7: 118,268,440 (GRCm39) |
I836N |
probably damaging |
Het |
Tmem100 |
T |
A |
11: 89,926,302 (GRCm39) |
M43K |
probably benign |
Het |
Ulk2 |
A |
G |
11: 61,745,378 (GRCm39) |
Y9H |
probably damaging |
Het |
Usp7 |
T |
C |
16: 8,523,027 (GRCm39) |
K311E |
probably damaging |
Het |
Vmn1r238 |
G |
A |
18: 3,123,033 (GRCm39) |
T127I |
probably benign |
Het |
Vmn2r28 |
T |
C |
7: 5,496,678 (GRCm39) |
Y58C |
probably damaging |
Het |
Wdr55 |
G |
A |
18: 36,893,469 (GRCm39) |
G44S |
probably benign |
Het |
Zfp677 |
C |
A |
17: 21,617,647 (GRCm39) |
H235N |
probably damaging |
Het |
Zfp869 |
T |
A |
8: 70,159,636 (GRCm39) |
R312S |
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 |
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 |
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 |
|