Other mutations in this stock |
Total: 112 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921524L21Rik |
G |
C |
18: 6,623,470 (GRCm39) |
R60P |
possibly damaging |
Het |
Aox1 |
T |
A |
1: 58,393,354 (GRCm39) |
C1199S |
probably benign |
Het |
Arhgap18 |
G |
A |
10: 26,763,857 (GRCm39) |
M482I |
probably damaging |
Het |
Arhgap18 |
G |
T |
10: 26,763,858 (GRCm39) |
A483S |
probably damaging |
Het |
Arid4a |
G |
A |
12: 71,122,112 (GRCm39) |
S509N |
probably benign |
Het |
BC051019 |
T |
C |
7: 109,322,381 (GRCm39) |
T38A |
probably benign |
Het |
Bcam |
T |
C |
7: 19,499,543 (GRCm39) |
N192S |
probably null |
Het |
Bend5 |
A |
T |
4: 111,311,438 (GRCm39) |
K351* |
probably null |
Het |
Bicdl2 |
T |
A |
17: 23,884,923 (GRCm39) |
M208K |
probably damaging |
Het |
Ccp110 |
A |
T |
7: 118,325,247 (GRCm39) |
|
probably null |
Het |
Cdc6 |
A |
T |
11: 98,803,043 (GRCm39) |
T328S |
probably damaging |
Het |
Cdk5rap2 |
G |
T |
4: 70,225,470 (GRCm39) |
N558K |
probably benign |
Het |
Cdkn1c |
C |
T |
7: 143,012,858 (GRCm39) |
R146K |
probably benign |
Het |
Ceacam18 |
G |
A |
7: 43,297,918 (GRCm39) |
C371Y |
probably benign |
Het |
Cep95 |
T |
A |
11: 106,697,177 (GRCm39) |
C233* |
probably null |
Het |
Chrnd |
A |
G |
1: 87,122,650 (GRCm39) |
I144V |
probably benign |
Het |
Col6a4 |
T |
A |
9: 105,957,299 (GRCm39) |
Q175L |
probably benign |
Het |
Cym |
A |
T |
3: 107,120,816 (GRCm39) |
V263E |
probably damaging |
Het |
Cyp2a4 |
G |
T |
7: 26,012,197 (GRCm39) |
V327F |
possibly damaging |
Het |
Dhx29 |
T |
A |
13: 113,084,774 (GRCm39) |
M664K |
probably damaging |
Het |
Dlec1 |
T |
G |
9: 118,975,075 (GRCm39) |
|
probably null |
Het |
Dna2 |
T |
C |
10: 62,792,863 (GRCm39) |
Y293H |
probably benign |
Het |
Dnase1l3 |
T |
A |
14: 7,974,104 (GRCm38) |
N196Y |
probably damaging |
Het |
Eea1 |
T |
A |
10: 95,832,822 (GRCm39) |
D222E |
probably damaging |
Het |
Efcab14 |
A |
T |
4: 115,610,116 (GRCm39) |
|
probably null |
Het |
Entpd5 |
C |
T |
12: 84,432,985 (GRCm39) |
R189H |
probably benign |
Het |
Exoc4 |
A |
T |
6: 33,734,985 (GRCm39) |
K534M |
probably damaging |
Het |
Extl1 |
T |
A |
4: 134,098,449 (GRCm39) |
Y194F |
probably benign |
Het |
Eya1 |
A |
G |
1: 14,323,299 (GRCm39) |
L161S |
possibly damaging |
Het |
Fam163b |
T |
C |
2: 27,002,874 (GRCm39) |
E41G |
possibly damaging |
Het |
Fam180a |
A |
C |
6: 35,292,287 (GRCm39) |
S40A |
probably benign |
Het |
Fbxl4 |
T |
C |
4: 22,385,950 (GRCm39) |
S186P |
probably benign |
Het |
Fbxw19 |
A |
T |
9: 109,323,840 (GRCm39) |
L45* |
probably null |
Het |
Fgf14 |
G |
T |
14: 124,913,924 (GRCm39) |
T69N |
probably benign |
Het |
Flt1 |
A |
G |
5: 147,609,519 (GRCm39) |
Y432H |
probably damaging |
Het |
Frmd4b |
A |
T |
6: 97,283,725 (GRCm39) |
L374Q |
possibly damaging |
Het |
G6pc2 |
T |
A |
2: 69,053,321 (GRCm39) |
V125D |
probably damaging |
Het |
Gm10033 |
T |
C |
8: 69,826,210 (GRCm39) |
I119M |
unknown |
Het |
Gna15 |
A |
T |
10: 81,347,954 (GRCm39) |
L164Q |
probably damaging |
Het |
Gnaz |
C |
A |
10: 74,827,702 (GRCm39) |
D151E |
possibly damaging |
Het |
Has1 |
T |
C |
17: 18,070,562 (GRCm39) |
T120A |
probably benign |
Het |
Hectd4 |
T |
A |
5: 121,496,366 (GRCm39) |
D3919E |
possibly damaging |
Het |
Hs3st5 |
A |
G |
10: 36,709,165 (GRCm39) |
I233M |
probably benign |
Het |
Ilf3 |
T |
C |
9: 21,314,438 (GRCm39) |
|
probably benign |
Het |
Inpp5b |
T |
A |
4: 124,687,069 (GRCm39) |
L765* |
probably null |
Het |
Insr |
A |
T |
8: 3,209,561 (GRCm39) |
I1174N |
probably damaging |
Het |
Kash5 |
T |
A |
7: 44,838,227 (GRCm39) |
|
probably null |
Het |
Kcnq3 |
A |
G |
15: 65,877,755 (GRCm39) |
L445P |
probably damaging |
Het |
Kctd20 |
A |
T |
17: 29,181,824 (GRCm39) |
N159Y |
probably damaging |
Het |
Kctd20 |
A |
T |
17: 29,185,755 (GRCm39) |
D366V |
probably damaging |
Het |
Klk15 |
T |
C |
7: 43,587,757 (GRCm39) |
|
probably benign |
Het |
Lama4 |
T |
G |
10: 38,979,497 (GRCm39) |
N1658K |
possibly damaging |
Het |
Lonrf2 |
G |
A |
1: 38,852,357 (GRCm39) |
P165S |
probably benign |
Het |
Mas1 |
T |
C |
17: 13,060,586 (GRCm39) |
Y279C |
probably damaging |
Het |
Mast2 |
G |
T |
4: 116,164,156 (GRCm39) |
D1747E |
probably damaging |
Het |
Mest |
G |
A |
6: 30,745,138 (GRCm39) |
M235I |
probably benign |
Het |
Mfsd6 |
A |
G |
1: 52,699,964 (GRCm39) |
|
probably null |
Het |
Mllt10 |
T |
A |
2: 18,167,657 (GRCm39) |
S449R |
probably damaging |
Het |
Mon2 |
T |
A |
10: 122,849,668 (GRCm39) |
T1211S |
probably benign |
Het |
Mrnip |
G |
A |
11: 50,067,688 (GRCm39) |
C27Y |
probably damaging |
Het |
Myh15 |
A |
T |
16: 48,983,498 (GRCm39) |
T1538S |
probably benign |
Het |
Nfatc2ip |
A |
G |
7: 125,989,634 (GRCm39) |
V250A |
probably benign |
Het |
Npy1r |
A |
G |
8: 67,157,177 (GRCm39) |
D199G |
possibly damaging |
Het |
Numbl |
A |
G |
7: 26,980,379 (GRCm39) |
T454A |
probably benign |
Het |
Nutm2 |
T |
G |
13: 50,627,152 (GRCm39) |
F436V |
probably damaging |
Het |
Opa1 |
T |
C |
16: 29,439,628 (GRCm39) |
S773P |
probably benign |
Het |
Or12e1 |
T |
A |
2: 87,022,042 (GRCm39) |
S4T |
probably benign |
Het |
Or2d3 |
A |
T |
7: 106,491,184 (GRCm39) |
|
probably null |
Het |
Or2d3 |
G |
T |
7: 106,491,185 (GRCm39) |
L44M |
probably damaging |
Het |
Or2r11 |
A |
G |
6: 42,437,611 (GRCm39) |
L114S |
probably damaging |
Het |
Or2t48 |
A |
G |
11: 58,420,602 (GRCm39) |
L70P |
probably damaging |
Het |
Or51b17 |
A |
G |
7: 103,542,484 (GRCm39) |
S153P |
probably benign |
Het |
Or51m1 |
C |
T |
7: 103,578,932 (GRCm39) |
R301* |
probably null |
Het |
Or52e7 |
A |
G |
7: 104,685,157 (GRCm39) |
S251G |
probably benign |
Het |
Or52i2 |
A |
G |
7: 102,319,508 (GRCm39) |
Y127C |
probably damaging |
Het |
Or8b12c |
T |
A |
9: 37,715,599 (GRCm39) |
Y131N |
probably damaging |
Het |
Pde8a |
G |
C |
7: 80,950,471 (GRCm39) |
|
probably null |
Het |
Pgam1 |
T |
C |
19: 41,906,144 (GRCm39) |
F232S |
probably damaging |
Het |
Pgk1 |
T |
A |
X: 105,243,914 (GRCm39) |
V303E |
possibly damaging |
Het |
Pirb |
A |
T |
7: 3,720,189 (GRCm39) |
C395S |
probably damaging |
Het |
Plxnc1 |
C |
T |
10: 94,680,184 (GRCm39) |
V824I |
probably benign |
Het |
Ppp6r1 |
A |
G |
7: 4,636,691 (GRCm39) |
|
probably null |
Het |
Rapgef4 |
C |
A |
2: 72,056,131 (GRCm39) |
|
probably benign |
Het |
Rars1 |
T |
A |
11: 35,700,465 (GRCm39) |
T539S |
probably damaging |
Het |
Rbm44 |
G |
T |
1: 91,081,679 (GRCm39) |
|
probably null |
Het |
Samd4b |
A |
G |
7: 28,113,317 (GRCm39) |
I216T |
probably benign |
Het |
Serpine2 |
A |
C |
1: 79,794,532 (GRCm39) |
F134V |
probably damaging |
Het |
Shmt1 |
A |
G |
11: 60,683,790 (GRCm39) |
Y341H |
probably damaging |
Het |
Slc23a2 |
C |
A |
2: 131,917,561 (GRCm39) |
V226F |
probably benign |
Het |
Slc23a4 |
A |
G |
6: 34,933,896 (GRCm39) |
I69T |
probably damaging |
Het |
Slc37a1 |
C |
A |
17: 31,552,652 (GRCm39) |
T319K |
possibly damaging |
Het |
Slc6a4 |
A |
T |
11: 76,904,078 (GRCm39) |
T178S |
probably damaging |
Het |
Smarca4 |
G |
A |
9: 21,612,479 (GRCm39) |
A1588T |
possibly damaging |
Het |
Spag17 |
A |
T |
3: 99,934,668 (GRCm39) |
Y650F |
possibly damaging |
Het |
Stambpl1 |
C |
G |
19: 34,204,121 (GRCm39) |
N70K |
probably damaging |
Het |
Stip1 |
C |
A |
19: 6,999,165 (GRCm39) |
C471F |
probably damaging |
Het |
Taf1 |
T |
C |
X: 100,584,500 (GRCm39) |
S223P |
probably benign |
Het |
Tchh |
C |
A |
3: 93,350,882 (GRCm39) |
N107K |
possibly damaging |
Het |
Tenm3 |
A |
C |
8: 48,685,139 (GRCm39) |
H2432Q |
probably damaging |
Het |
Tmem243 |
A |
G |
5: 9,168,548 (GRCm39) |
N110S |
probably damaging |
Het |
Toe1 |
A |
T |
4: 116,662,076 (GRCm39) |
I306F |
probably benign |
Het |
Trank1 |
G |
A |
9: 111,221,995 (GRCm39) |
V2911M |
probably damaging |
Het |
Trpm4 |
A |
G |
7: 44,958,036 (GRCm39) |
I811T |
probably damaging |
Het |
Tspear |
T |
A |
10: 77,710,950 (GRCm39) |
|
probably null |
Het |
Ttc28 |
A |
T |
5: 111,425,034 (GRCm39) |
I1589F |
possibly damaging |
Het |
Tubgcp3 |
A |
G |
8: 12,699,686 (GRCm39) |
|
probably benign |
Het |
U2af2 |
C |
A |
7: 5,070,544 (GRCm39) |
R78S |
probably benign |
Het |
Wdr17 |
A |
T |
8: 55,126,689 (GRCm39) |
D388E |
possibly damaging |
Het |
Wdr3 |
A |
T |
3: 100,061,186 (GRCm39) |
S261T |
probably benign |
Het |
Zfp667 |
A |
G |
7: 6,308,066 (GRCm39) |
N245D |
possibly damaging |
Het |
Zfp692 |
A |
G |
11: 58,201,002 (GRCm39) |
|
probably benign |
Het |
Zfp729a |
T |
C |
13: 67,767,370 (GRCm39) |
H953R |
probably benign |
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 |
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 |
R9756:Stab2
|
UTSW |
10 |
86,803,553 (GRCm39) |
missense |
possibly damaging |
0.50 |
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 |
|