Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700066M21Rik |
A |
T |
1: 57,421,906 (GRCm39) |
Y94F |
possibly damaging |
Het |
Abcb5 |
A |
G |
12: 118,881,873 (GRCm39) |
S619P |
probably damaging |
Het |
Adgrf5 |
A |
G |
17: 43,761,137 (GRCm39) |
N944S |
probably benign |
Het |
Ano1 |
T |
A |
7: 144,162,666 (GRCm39) |
M689L |
probably benign |
Het |
Antxr1 |
T |
A |
6: 87,217,936 (GRCm39) |
H314L |
probably benign |
Het |
Atp13a5 |
CA |
C |
16: 29,051,583 (GRCm39) |
|
probably null |
Het |
Blmh |
T |
A |
11: 76,859,509 (GRCm39) |
M370K |
probably damaging |
Het |
Cdh8 |
G |
A |
8: 99,759,976 (GRCm39) |
T591M |
probably damaging |
Het |
Cep290 |
G |
A |
10: 100,352,034 (GRCm39) |
E747K |
probably damaging |
Het |
Chd6 |
T |
C |
2: 160,802,259 (GRCm39) |
S2192G |
probably benign |
Het |
Cldn8 |
T |
G |
16: 88,359,917 (GRCm39) |
T3P |
probably benign |
Het |
Crtac1 |
A |
G |
19: 42,286,780 (GRCm39) |
L421P |
probably damaging |
Het |
Ddx59 |
G |
T |
1: 136,345,069 (GRCm39) |
A247S |
probably damaging |
Het |
Defa38 |
C |
T |
8: 21,585,943 (GRCm39) |
V42I |
possibly damaging |
Het |
Dennd5a |
A |
G |
7: 109,496,174 (GRCm39) |
V1164A |
possibly damaging |
Het |
Dnhd1 |
A |
T |
7: 105,353,135 (GRCm39) |
T2763S |
probably benign |
Het |
Evpl |
T |
C |
11: 116,112,077 (GRCm39) |
D1871G |
probably damaging |
Het |
Fat1 |
T |
A |
8: 45,496,974 (GRCm39) |
I4153N |
probably damaging |
Het |
Fbxl17 |
A |
G |
17: 63,367,310 (GRCm39) |
Y688H |
probably damaging |
Het |
Fntb |
A |
G |
12: 76,966,938 (GRCm39) |
E424G |
probably benign |
Het |
Gabra4 |
A |
G |
5: 71,729,067 (GRCm39) |
M571T |
probably damaging |
Het |
Hoxb5 |
T |
C |
11: 96,194,449 (GRCm39) |
Y4H |
probably damaging |
Het |
Htr1a |
T |
C |
13: 105,581,450 (GRCm39) |
V230A |
probably damaging |
Het |
Idh2 |
TCCCAGG |
T |
7: 79,748,079 (GRCm39) |
|
probably benign |
Het |
Ighv3-4 |
T |
C |
12: 114,217,448 (GRCm39) |
T48A |
probably damaging |
Het |
Il15ra |
A |
G |
2: 11,728,259 (GRCm39) |
M53V |
probably benign |
Het |
Ipo9 |
A |
C |
1: 135,314,057 (GRCm39) |
D945E |
probably benign |
Het |
Klk1b22 |
A |
T |
7: 43,765,254 (GRCm39) |
|
probably null |
Het |
Klkb1 |
T |
C |
8: 45,735,811 (GRCm39) |
N184S |
possibly damaging |
Het |
Lbhd2 |
G |
A |
12: 111,376,774 (GRCm39) |
A74T |
probably damaging |
Het |
Lpcat3 |
A |
G |
6: 124,679,967 (GRCm39) |
|
probably null |
Het |
Luzp1 |
T |
C |
4: 136,270,048 (GRCm39) |
I757T |
probably damaging |
Het |
Mbd5 |
C |
A |
2: 49,169,283 (GRCm39) |
P1485T |
probably benign |
Het |
Mfsd14b |
C |
A |
13: 65,221,414 (GRCm39) |
V293L |
probably benign |
Het |
Mical2 |
C |
T |
7: 111,902,928 (GRCm39) |
T133I |
probably damaging |
Het |
Mylk |
T |
C |
16: 34,734,387 (GRCm39) |
S663P |
probably damaging |
Het |
Or2ag13 |
A |
T |
7: 106,313,002 (GRCm39) |
N295K |
probably benign |
Het |
Or2j3 |
A |
G |
17: 38,615,971 (GRCm39) |
V127A |
probably benign |
Het |
Or4x11 |
A |
T |
2: 89,867,674 (GRCm39) |
N137I |
probably benign |
Het |
Or5ak22 |
T |
A |
2: 85,230,682 (GRCm39) |
H65L |
probably damaging |
Het |
Or5b119 |
G |
A |
19: 13,456,986 (GRCm39) |
T192I |
probably benign |
Het |
Or8b12 |
G |
A |
9: 37,658,314 (GRCm39) |
D295N |
possibly damaging |
Het |
Patj |
G |
T |
4: 98,565,535 (GRCm39) |
A1656S |
probably benign |
Het |
Peg10 |
GC |
GCGCC |
6: 4,756,452 (GRCm39) |
|
probably benign |
Het |
Pigz |
G |
T |
16: 31,763,787 (GRCm39) |
G282C |
probably damaging |
Het |
Pomk |
G |
A |
8: 26,472,918 (GRCm39) |
T345M |
possibly damaging |
Het |
Psap |
T |
C |
10: 60,130,784 (GRCm39) |
S205P |
possibly damaging |
Het |
Ptpn6 |
A |
T |
6: 124,705,592 (GRCm39) |
F186L |
probably damaging |
Het |
Rnase2b |
T |
C |
14: 51,400,302 (GRCm39) |
S128P |
probably damaging |
Het |
Rnf112 |
C |
T |
11: 61,340,667 (GRCm39) |
V536I |
probably damaging |
Het |
Rnf31 |
A |
T |
14: 55,836,582 (GRCm39) |
E805D |
probably damaging |
Het |
Rps6kc1 |
A |
T |
1: 190,604,021 (GRCm39) |
D200E |
probably benign |
Het |
Rufy2 |
T |
C |
10: 62,818,519 (GRCm39) |
L25P |
probably damaging |
Het |
Sec14l2 |
T |
A |
11: 4,053,978 (GRCm39) |
K230* |
probably null |
Het |
Senp1 |
A |
G |
15: 97,957,806 (GRCm39) |
I364T |
possibly damaging |
Het |
Sod1 |
T |
A |
16: 90,017,753 (GRCm39) |
M3K |
probably benign |
Het |
Tcf4 |
G |
T |
18: 69,790,830 (GRCm39) |
E408* |
probably null |
Het |
Tdrd1 |
T |
C |
19: 56,831,662 (GRCm39) |
M351T |
probably benign |
Het |
Tmem39a |
T |
C |
16: 38,396,126 (GRCm39) |
Y120H |
probably benign |
Het |
Trav16 |
C |
A |
14: 53,980,886 (GRCm39) |
T25K |
possibly damaging |
Het |
Unc13c |
T |
A |
9: 73,839,526 (GRCm39) |
N442Y |
probably benign |
Het |
Vmn2r71 |
A |
T |
7: 85,268,573 (GRCm39) |
K259* |
probably null |
Het |
Yipf1 |
T |
C |
4: 107,176,247 (GRCm39) |
V47A |
probably benign |
Het |
Zeb2 |
T |
C |
2: 44,887,414 (GRCm39) |
T548A |
possibly damaging |
Het |
Zmym4 |
A |
G |
4: 126,771,502 (GRCm39) |
F1291L |
probably damaging |
Het |
|
Other mutations in Stab2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00091:Stab2
|
APN |
10 |
86,705,070 (GRCm39) |
splice site |
probably null |
|
IGL00809:Stab2
|
APN |
10 |
86,684,038 (GRCm39) |
splice site |
probably benign |
|
IGL00911:Stab2
|
APN |
10 |
86,805,617 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01347:Stab2
|
APN |
10 |
86,737,567 (GRCm39) |
splice site |
probably null |
|
IGL01411:Stab2
|
APN |
10 |
86,815,872 (GRCm39) |
splice site |
probably benign |
|
IGL01503:Stab2
|
APN |
10 |
86,776,477 (GRCm39) |
splice site |
probably benign |
|
IGL01599:Stab2
|
APN |
10 |
86,758,759 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01635:Stab2
|
APN |
10 |
86,816,992 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01640:Stab2
|
APN |
10 |
86,790,035 (GRCm39) |
missense |
probably benign |
0.09 |
IGL01671:Stab2
|
APN |
10 |
86,805,141 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02023:Stab2
|
APN |
10 |
86,707,695 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02075:Stab2
|
APN |
10 |
86,803,514 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02174:Stab2
|
APN |
10 |
86,695,606 (GRCm39) |
splice site |
probably null |
|
IGL02600:Stab2
|
APN |
10 |
86,790,123 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02666:Stab2
|
APN |
10 |
86,686,766 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02668:Stab2
|
APN |
10 |
86,682,027 (GRCm39) |
splice site |
probably benign |
|
IGL02709:Stab2
|
APN |
10 |
86,682,029 (GRCm39) |
splice site |
probably benign |
|
IGL02728:Stab2
|
APN |
10 |
86,692,420 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02803:Stab2
|
APN |
10 |
86,786,133 (GRCm39) |
splice site |
probably benign |
|
IGL02938:Stab2
|
APN |
10 |
86,707,785 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL03033:Stab2
|
APN |
10 |
86,832,667 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03238:Stab2
|
APN |
10 |
86,690,985 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03402:Stab2
|
APN |
10 |
86,805,165 (GRCm39) |
missense |
probably benign |
0.03 |
prospector
|
UTSW |
10 |
86,737,431 (GRCm39) |
splice site |
probably null |
|
songbird
|
UTSW |
10 |
86,694,016 (GRCm39) |
missense |
probably damaging |
1.00 |
3-1:Stab2
|
UTSW |
10 |
86,705,041 (GRCm39) |
missense |
probably damaging |
0.96 |
F6893:Stab2
|
UTSW |
10 |
86,691,035 (GRCm39) |
missense |
probably damaging |
1.00 |
K7371:Stab2
|
UTSW |
10 |
86,779,153 (GRCm39) |
critical splice donor site |
probably null |
|
PIT4142001:Stab2
|
UTSW |
10 |
86,703,039 (GRCm39) |
missense |
possibly damaging |
0.94 |
PIT4362001:Stab2
|
UTSW |
10 |
86,697,299 (GRCm39) |
nonsense |
probably null |
|
R0015:Stab2
|
UTSW |
10 |
86,679,481 (GRCm39) |
missense |
probably benign |
|
R0254:Stab2
|
UTSW |
10 |
86,733,824 (GRCm39) |
missense |
probably benign |
|
R0310:Stab2
|
UTSW |
10 |
86,803,477 (GRCm39) |
splice site |
probably benign |
|
R0333:Stab2
|
UTSW |
10 |
86,677,491 (GRCm39) |
missense |
probably benign |
|
R0391:Stab2
|
UTSW |
10 |
86,783,008 (GRCm39) |
missense |
probably benign |
0.27 |
R0400:Stab2
|
UTSW |
10 |
86,708,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R0433:Stab2
|
UTSW |
10 |
86,679,355 (GRCm39) |
splice site |
probably benign |
|
R0440:Stab2
|
UTSW |
10 |
86,785,792 (GRCm39) |
missense |
probably benign |
0.23 |
R0743:Stab2
|
UTSW |
10 |
86,723,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R0847:Stab2
|
UTSW |
10 |
86,805,735 (GRCm39) |
missense |
probably benign |
0.00 |
R0883:Stab2
|
UTSW |
10 |
86,760,314 (GRCm39) |
splice site |
probably benign |
|
R1078:Stab2
|
UTSW |
10 |
86,742,997 (GRCm39) |
splice site |
probably null |
|
R1118:Stab2
|
UTSW |
10 |
86,721,582 (GRCm39) |
splice site |
probably null |
|
R1119:Stab2
|
UTSW |
10 |
86,695,619 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1179:Stab2
|
UTSW |
10 |
86,786,165 (GRCm39) |
missense |
probably damaging |
0.98 |
R1440:Stab2
|
UTSW |
10 |
86,697,231 (GRCm39) |
splice site |
probably null |
|
R1550:Stab2
|
UTSW |
10 |
86,714,790 (GRCm39) |
missense |
probably benign |
0.01 |
R1616:Stab2
|
UTSW |
10 |
86,721,582 (GRCm39) |
splice site |
probably null |
|
R1728:Stab2
|
UTSW |
10 |
86,773,903 (GRCm39) |
missense |
probably benign |
0.41 |
R1768:Stab2
|
UTSW |
10 |
86,838,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R1772:Stab2
|
UTSW |
10 |
86,790,098 (GRCm39) |
missense |
probably benign |
0.06 |
R1776:Stab2
|
UTSW |
10 |
86,793,680 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1784:Stab2
|
UTSW |
10 |
86,773,903 (GRCm39) |
missense |
probably benign |
0.41 |
R1892:Stab2
|
UTSW |
10 |
86,773,913 (GRCm39) |
missense |
probably damaging |
0.99 |
R1957:Stab2
|
UTSW |
10 |
86,697,334 (GRCm39) |
missense |
probably benign |
0.13 |
R1972:Stab2
|
UTSW |
10 |
86,796,180 (GRCm39) |
missense |
probably damaging |
0.99 |
R1975:Stab2
|
UTSW |
10 |
86,732,360 (GRCm39) |
critical splice donor site |
probably null |
|
R1976:Stab2
|
UTSW |
10 |
86,732,360 (GRCm39) |
critical splice donor site |
probably null |
|
R1996:Stab2
|
UTSW |
10 |
86,838,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R2085:Stab2
|
UTSW |
10 |
86,790,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R2149:Stab2
|
UTSW |
10 |
86,700,904 (GRCm39) |
nonsense |
probably null |
|
R2169:Stab2
|
UTSW |
10 |
86,723,726 (GRCm39) |
missense |
probably damaging |
1.00 |
R2201:Stab2
|
UTSW |
10 |
86,776,503 (GRCm39) |
missense |
probably benign |
0.22 |
R2296:Stab2
|
UTSW |
10 |
86,790,338 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2297:Stab2
|
UTSW |
10 |
86,790,338 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2298:Stab2
|
UTSW |
10 |
86,790,338 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2326:Stab2
|
UTSW |
10 |
86,790,338 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2434:Stab2
|
UTSW |
10 |
86,805,183 (GRCm39) |
missense |
possibly damaging |
0.78 |
R2519:Stab2
|
UTSW |
10 |
86,770,704 (GRCm39) |
splice site |
probably benign |
|
R2696:Stab2
|
UTSW |
10 |
86,697,363 (GRCm39) |
missense |
probably benign |
0.45 |
R2883:Stab2
|
UTSW |
10 |
86,803,550 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2923:Stab2
|
UTSW |
10 |
86,697,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R3711:Stab2
|
UTSW |
10 |
86,702,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R3787:Stab2
|
UTSW |
10 |
86,805,141 (GRCm39) |
missense |
possibly damaging |
0.50 |
R3834:Stab2
|
UTSW |
10 |
86,785,776 (GRCm39) |
missense |
possibly damaging |
0.87 |
R3970:Stab2
|
UTSW |
10 |
86,714,750 (GRCm39) |
missense |
probably damaging |
0.97 |
R3979:Stab2
|
UTSW |
10 |
86,699,320 (GRCm39) |
missense |
possibly damaging |
0.56 |
R4003:Stab2
|
UTSW |
10 |
86,693,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R4088:Stab2
|
UTSW |
10 |
86,758,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R4151:Stab2
|
UTSW |
10 |
86,838,847 (GRCm39) |
missense |
probably benign |
0.12 |
R4190:Stab2
|
UTSW |
10 |
86,714,808 (GRCm39) |
missense |
probably damaging |
0.98 |
R4556:Stab2
|
UTSW |
10 |
86,803,543 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4773:Stab2
|
UTSW |
10 |
86,743,235 (GRCm39) |
nonsense |
probably null |
|
R4825:Stab2
|
UTSW |
10 |
86,783,011 (GRCm39) |
missense |
probably benign |
0.08 |
R4865:Stab2
|
UTSW |
10 |
86,679,364 (GRCm39) |
splice site |
probably null |
|
R4871:Stab2
|
UTSW |
10 |
86,778,099 (GRCm39) |
missense |
probably damaging |
0.99 |
R4943:Stab2
|
UTSW |
10 |
86,790,026 (GRCm39) |
missense |
probably damaging |
0.99 |
R4981:Stab2
|
UTSW |
10 |
86,796,087 (GRCm39) |
missense |
probably benign |
|
R4994:Stab2
|
UTSW |
10 |
86,785,771 (GRCm39) |
missense |
probably benign |
|
R4999:Stab2
|
UTSW |
10 |
86,773,773 (GRCm39) |
missense |
probably damaging |
0.97 |
R5061:Stab2
|
UTSW |
10 |
86,743,249 (GRCm39) |
missense |
probably damaging |
1.00 |
R5072:Stab2
|
UTSW |
10 |
86,699,422 (GRCm39) |
missense |
probably benign |
0.23 |
R5073:Stab2
|
UTSW |
10 |
86,699,422 (GRCm39) |
missense |
probably benign |
0.23 |
R5074:Stab2
|
UTSW |
10 |
86,699,422 (GRCm39) |
missense |
probably benign |
0.23 |
R5134:Stab2
|
UTSW |
10 |
86,707,674 (GRCm39) |
splice site |
probably null |
|
R5213:Stab2
|
UTSW |
10 |
86,743,061 (GRCm39) |
missense |
probably damaging |
0.99 |
R5508:Stab2
|
UTSW |
10 |
86,796,143 (GRCm39) |
missense |
probably benign |
0.01 |
R5530:Stab2
|
UTSW |
10 |
86,783,026 (GRCm39) |
missense |
probably benign |
0.04 |
R5540:Stab2
|
UTSW |
10 |
86,683,989 (GRCm39) |
missense |
probably benign |
0.30 |
R5839:Stab2
|
UTSW |
10 |
86,708,555 (GRCm39) |
missense |
probably damaging |
0.97 |
R5949:Stab2
|
UTSW |
10 |
86,805,713 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6015:Stab2
|
UTSW |
10 |
86,773,906 (GRCm39) |
missense |
probably damaging |
0.99 |
R6019:Stab2
|
UTSW |
10 |
86,838,886 (GRCm39) |
missense |
probably benign |
0.00 |
R6116:Stab2
|
UTSW |
10 |
86,743,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R6131:Stab2
|
UTSW |
10 |
86,719,642 (GRCm39) |
splice site |
probably null |
|
R6209:Stab2
|
UTSW |
10 |
86,758,867 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6243:Stab2
|
UTSW |
10 |
86,743,025 (GRCm39) |
missense |
probably damaging |
1.00 |
R6433:Stab2
|
UTSW |
10 |
86,737,431 (GRCm39) |
splice site |
probably null |
|
R6787:Stab2
|
UTSW |
10 |
86,754,948 (GRCm39) |
missense |
probably benign |
0.07 |
R6841:Stab2
|
UTSW |
10 |
86,778,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R6873:Stab2
|
UTSW |
10 |
86,697,230 (GRCm39) |
critical splice donor site |
probably null |
|
R7025:Stab2
|
UTSW |
10 |
86,686,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R7043:Stab2
|
UTSW |
10 |
86,706,110 (GRCm39) |
missense |
probably damaging |
0.99 |
R7047:Stab2
|
UTSW |
10 |
86,694,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R7107:Stab2
|
UTSW |
10 |
86,741,456 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7214:Stab2
|
UTSW |
10 |
86,735,705 (GRCm39) |
missense |
probably damaging |
0.99 |
R7271:Stab2
|
UTSW |
10 |
86,838,972 (GRCm39) |
splice site |
probably null |
|
R7291:Stab2
|
UTSW |
10 |
86,782,084 (GRCm39) |
missense |
probably damaging |
0.96 |
R7336:Stab2
|
UTSW |
10 |
86,805,049 (GRCm39) |
nonsense |
probably null |
|
R7432:Stab2
|
UTSW |
10 |
86,721,547 (GRCm39) |
missense |
probably damaging |
0.99 |
R7580:Stab2
|
UTSW |
10 |
86,705,028 (GRCm39) |
missense |
probably benign |
0.00 |
R7622:Stab2
|
UTSW |
10 |
86,709,766 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7629:Stab2
|
UTSW |
10 |
86,719,646 (GRCm39) |
critical splice donor site |
probably null |
|
R7658:Stab2
|
UTSW |
10 |
86,816,999 (GRCm39) |
missense |
probably benign |
0.12 |
R7798:Stab2
|
UTSW |
10 |
86,793,776 (GRCm39) |
missense |
probably damaging |
0.98 |
R7835:Stab2
|
UTSW |
10 |
86,708,483 (GRCm39) |
missense |
probably benign |
0.06 |
R7845:Stab2
|
UTSW |
10 |
86,832,758 (GRCm39) |
missense |
probably benign |
0.09 |
R7863:Stab2
|
UTSW |
10 |
86,808,745 (GRCm39) |
missense |
probably benign |
0.30 |
R7885:Stab2
|
UTSW |
10 |
86,714,776 (GRCm39) |
missense |
probably benign |
0.03 |
R7904:Stab2
|
UTSW |
10 |
86,790,056 (GRCm39) |
nonsense |
probably null |
|
R7947:Stab2
|
UTSW |
10 |
86,681,897 (GRCm39) |
missense |
probably benign |
0.31 |
R7963:Stab2
|
UTSW |
10 |
86,683,887 (GRCm39) |
critical splice donor site |
probably null |
|
R8014:Stab2
|
UTSW |
10 |
86,686,767 (GRCm39) |
missense |
possibly damaging |
0.78 |
R8021:Stab2
|
UTSW |
10 |
86,741,403 (GRCm39) |
missense |
possibly damaging |
0.69 |
R8024:Stab2
|
UTSW |
10 |
86,681,916 (GRCm39) |
missense |
probably benign |
0.34 |
R8097:Stab2
|
UTSW |
10 |
86,704,959 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8281:Stab2
|
UTSW |
10 |
86,709,728 (GRCm39) |
missense |
probably damaging |
0.98 |
R8462:Stab2
|
UTSW |
10 |
86,803,598 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8670:Stab2
|
UTSW |
10 |
86,776,587 (GRCm39) |
missense |
probably damaging |
1.00 |
R8692:Stab2
|
UTSW |
10 |
86,808,794 (GRCm39) |
missense |
probably damaging |
0.99 |
R8744:Stab2
|
UTSW |
10 |
86,805,213 (GRCm39) |
missense |
probably benign |
0.32 |
R8745:Stab2
|
UTSW |
10 |
86,805,213 (GRCm39) |
missense |
probably benign |
0.32 |
R8782:Stab2
|
UTSW |
10 |
86,735,685 (GRCm39) |
missense |
probably benign |
0.00 |
R8875:Stab2
|
UTSW |
10 |
86,832,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R8978:Stab2
|
UTSW |
10 |
86,785,782 (GRCm39) |
missense |
possibly damaging |
0.64 |
R9141:Stab2
|
UTSW |
10 |
86,704,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R9248:Stab2
|
UTSW |
10 |
86,727,481 (GRCm39) |
missense |
probably damaging |
0.98 |
R9326:Stab2
|
UTSW |
10 |
86,791,010 (GRCm39) |
missense |
probably damaging |
1.00 |
R9426:Stab2
|
UTSW |
10 |
86,704,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R9568:Stab2
|
UTSW |
10 |
86,699,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R9627:Stab2
|
UTSW |
10 |
86,793,704 (GRCm39) |
missense |
probably damaging |
0.98 |
R9635:Stab2
|
UTSW |
10 |
86,686,651 (GRCm39) |
nonsense |
probably null |
|
R9648:Stab2
|
UTSW |
10 |
86,692,561 (GRCm39) |
frame shift |
probably null |
|
R9649:Stab2
|
UTSW |
10 |
86,692,561 (GRCm39) |
frame shift |
probably null |
|
R9650:Stab2
|
UTSW |
10 |
86,692,561 (GRCm39) |
frame shift |
probably null |
|
R9726:Stab2
|
UTSW |
10 |
86,790,095 (GRCm39) |
missense |
probably benign |
0.00 |
R9786:Stab2
|
UTSW |
10 |
86,757,997 (GRCm39) |
missense |
probably benign |
0.03 |
RF061:Stab2
|
UTSW |
10 |
86,702,622 (GRCm39) |
critical splice acceptor site |
probably benign |
|
X0023:Stab2
|
UTSW |
10 |
86,758,062 (GRCm39) |
critical splice acceptor site |
probably null |
|
X0025:Stab2
|
UTSW |
10 |
86,723,680 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Stab2
|
UTSW |
10 |
86,785,778 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Stab2
|
UTSW |
10 |
86,732,460 (GRCm39) |
missense |
probably damaging |
1.00 |
|