Other mutations in this stock |
Total: 96 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A630073D07Rik |
C |
T |
6: 132,604,434 (GRCm39) |
V4I |
unknown |
Het |
Actn1 |
A |
T |
12: 80,240,489 (GRCm39) |
D199E |
probably benign |
Het |
Adam17 |
T |
C |
12: 21,375,602 (GRCm39) |
D739G |
probably damaging |
Het |
Agmat |
T |
C |
4: 141,474,163 (GRCm39) |
S15P |
probably benign |
Het |
Ahsa2 |
A |
G |
11: 23,441,099 (GRCm39) |
S229P |
probably damaging |
Het |
Arhgef3 |
A |
G |
14: 26,987,535 (GRCm39) |
D36G |
possibly damaging |
Het |
C6 |
C |
A |
15: 4,826,404 (GRCm39) |
Y662* |
probably null |
Het |
Ccs |
T |
C |
19: 4,883,378 (GRCm39) |
D140G |
probably benign |
Het |
Cdc42bpb |
A |
G |
12: 111,312,039 (GRCm39) |
L65P |
probably damaging |
Het |
Cdh24 |
A |
T |
14: 54,876,378 (GRCm39) |
V149E |
possibly damaging |
Het |
Cdk12 |
C |
A |
11: 98,101,294 (GRCm39) |
S384* |
probably null |
Het |
Cep350 |
G |
A |
1: 155,777,237 (GRCm39) |
A1701V |
probably damaging |
Het |
Ces1g |
T |
C |
8: 94,060,307 (GRCm39) |
Q104R |
not run |
Het |
Chd5 |
A |
G |
4: 152,447,745 (GRCm39) |
H537R |
probably damaging |
Het |
Cln5 |
T |
A |
14: 103,313,339 (GRCm39) |
V197D |
probably damaging |
Het |
Coq7 |
A |
G |
7: 118,128,798 (GRCm39) |
V79A |
probably benign |
Het |
Cp |
A |
T |
3: 20,018,470 (GRCm39) |
N58I |
probably benign |
Het |
Cplx2 |
A |
T |
13: 54,526,639 (GRCm39) |
M16L |
probably benign |
Het |
Crot |
A |
G |
5: 9,027,534 (GRCm39) |
L266S |
probably damaging |
Het |
Ctbs |
T |
A |
3: 146,164,509 (GRCm39) |
Y221N |
probably damaging |
Het |
Cul7 |
T |
A |
17: 46,967,933 (GRCm39) |
L707Q |
probably damaging |
Het |
D430041D05Rik |
G |
A |
2: 104,085,363 (GRCm39) |
T378I |
possibly damaging |
Het |
Dixdc1 |
T |
C |
9: 50,599,953 (GRCm39) |
I364V |
probably damaging |
Het |
Dnah11 |
T |
A |
12: 117,982,477 (GRCm39) |
H2564L |
probably damaging |
Het |
Dnajc3 |
T |
C |
14: 119,175,576 (GRCm39) |
Y26H |
probably benign |
Het |
Dpysl2 |
G |
A |
14: 67,071,664 (GRCm39) |
H159Y |
possibly damaging |
Het |
Ehmt1 |
T |
A |
2: 24,746,713 (GRCm39) |
K423I |
possibly damaging |
Het |
Eif1ad4 |
A |
G |
12: 87,862,170 (GRCm39) |
N11D |
unknown |
Het |
Enpp7 |
A |
G |
11: 118,882,985 (GRCm39) |
N353S |
probably benign |
Het |
Ext1 |
G |
A |
15: 53,208,119 (GRCm39) |
A214V |
probably damaging |
Het |
Fbh1 |
A |
T |
2: 11,751,887 (GRCm39) |
I937N |
probably damaging |
Het |
Fbxo39 |
T |
C |
11: 72,207,800 (GRCm39) |
Y51H |
possibly damaging |
Het |
Firrm |
A |
T |
1: 163,813,602 (GRCm39) |
D207E |
possibly damaging |
Het |
Grem2 |
T |
C |
1: 174,664,514 (GRCm39) |
K112E |
probably benign |
Het |
Gucy1a1 |
A |
G |
3: 82,005,027 (GRCm39) |
V586A |
probably damaging |
Het |
Il12rb2 |
G |
T |
6: 67,280,450 (GRCm39) |
L586I |
possibly damaging |
Het |
Il18 |
T |
C |
9: 50,490,614 (GRCm39) |
I83T |
probably damaging |
Het |
Irs1 |
A |
T |
1: 82,266,835 (GRCm39) |
Y460* |
probably null |
Het |
Jak1 |
G |
T |
4: 101,041,536 (GRCm39) |
Q161K |
possibly damaging |
Het |
Jakmip1 |
T |
A |
5: 37,276,148 (GRCm39) |
L486Q |
probably damaging |
Het |
Jmjd1c |
C |
A |
10: 67,054,143 (GRCm39) |
Q16K |
probably benign |
Het |
Kidins220 |
T |
C |
12: 25,106,999 (GRCm39) |
L1393P |
probably benign |
Het |
Klhl24 |
A |
C |
16: 19,936,750 (GRCm39) |
I453L |
probably benign |
Het |
Krtap2-4 |
C |
T |
11: 99,505,420 (GRCm39) |
D64N |
probably damaging |
Het |
Man1a |
T |
A |
10: 53,784,105 (GRCm39) |
D592V |
probably damaging |
Het |
Mepe |
T |
A |
5: 104,485,009 (GRCm39) |
Y50N |
probably benign |
Het |
Mier3 |
G |
A |
13: 111,841,783 (GRCm39) |
G115S |
possibly damaging |
Het |
Muc4 |
T |
A |
16: 32,754,670 (GRCm38) |
S1515T |
probably benign |
Het |
Nalcn |
T |
C |
14: 123,529,251 (GRCm39) |
D1408G |
probably benign |
Het |
Nav1 |
T |
C |
1: 135,380,591 (GRCm39) |
M1443V |
unknown |
Het |
Nckap1l |
A |
C |
15: 103,379,709 (GRCm39) |
N332T |
possibly damaging |
Het |
Neurl4 |
T |
A |
11: 69,802,905 (GRCm39) |
L1467Q |
probably benign |
Het |
Notch2 |
A |
G |
3: 98,038,718 (GRCm39) |
N1287S |
probably benign |
Het |
Nr4a3 |
C |
T |
4: 48,083,203 (GRCm39) |
P579S |
probably benign |
Het |
Nrxn2 |
A |
T |
19: 6,567,112 (GRCm39) |
H1329L |
probably benign |
Het |
Nynrin |
A |
T |
14: 56,107,857 (GRCm39) |
H988L |
possibly damaging |
Het |
Or1e34 |
T |
A |
11: 73,778,827 (GRCm39) |
I124F |
probably damaging |
Het |
Or4c31 |
A |
G |
2: 88,291,836 (GRCm39) |
T70A |
probably benign |
Het |
Or4c3d |
A |
G |
2: 89,882,089 (GRCm39) |
I193T |
probably benign |
Het |
Or52e3 |
G |
T |
7: 102,869,830 (GRCm39) |
D302Y |
possibly damaging |
Het |
Or7g35 |
T |
A |
9: 19,495,856 (GRCm39) |
F8I |
probably benign |
Het |
Pclo |
G |
A |
5: 14,843,882 (GRCm39) |
S1534N |
probably damaging |
Het |
Pign |
A |
G |
1: 105,512,778 (GRCm39) |
V635A |
probably benign |
Het |
Pkhd1 |
T |
C |
1: 20,664,177 (GRCm39) |
T134A |
probably damaging |
Het |
Plcb4 |
A |
T |
2: 135,818,068 (GRCm39) |
N790I |
possibly damaging |
Het |
Plxna2 |
G |
T |
1: 194,482,087 (GRCm39) |
C1453F |
probably damaging |
Het |
Plxna4 |
A |
G |
6: 32,173,057 (GRCm39) |
|
probably null |
Het |
Pnpla2 |
A |
G |
7: 141,037,344 (GRCm39) |
I116V |
possibly damaging |
Het |
Polq |
A |
G |
16: 36,880,790 (GRCm39) |
T985A |
probably benign |
Het |
Pramel11 |
T |
C |
4: 143,622,456 (GRCm39) |
T300A |
possibly damaging |
Het |
Prex1 |
T |
C |
2: 166,555,490 (GRCm39) |
N50S |
probably benign |
Het |
Ptgfrn |
G |
A |
3: 100,984,760 (GRCm39) |
A144V |
probably benign |
Het |
Rad54b |
G |
A |
4: 11,599,782 (GRCm39) |
G329S |
probably damaging |
Het |
Rrbp1 |
A |
G |
2: 143,809,364 (GRCm39) |
L931S |
probably benign |
Het |
Saxo4 |
T |
G |
19: 10,456,943 (GRCm39) |
D134A |
probably damaging |
Het |
Sipa1l2 |
A |
G |
8: 126,180,071 (GRCm39) |
S1109P |
probably damaging |
Het |
Slc26a7 |
G |
T |
4: 14,546,305 (GRCm39) |
N341K |
probably damaging |
Het |
Smg1 |
A |
C |
7: 117,784,200 (GRCm39) |
D958E |
unknown |
Het |
Smg6 |
T |
A |
11: 74,820,979 (GRCm39) |
S417T |
probably benign |
Het |
Srgap3 |
A |
G |
6: 112,723,882 (GRCm39) |
V550A |
probably damaging |
Het |
Terb1 |
T |
A |
8: 105,195,431 (GRCm39) |
D570V |
probably damaging |
Het |
Tet3 |
A |
G |
6: 83,345,076 (GRCm39) |
V1787A |
probably benign |
Het |
Tor1a |
A |
T |
2: 30,853,753 (GRCm39) |
D192E |
probably benign |
Het |
Tpr |
T |
C |
1: 150,323,372 (GRCm39) |
S2379P |
possibly damaging |
Het |
Trip12 |
A |
T |
1: 84,728,163 (GRCm39) |
F1138L |
probably damaging |
Het |
Trpv1 |
T |
C |
11: 73,151,203 (GRCm39) |
L797P |
probably damaging |
Het |
Tut1 |
T |
C |
19: 8,942,698 (GRCm39) |
L595P |
probably damaging |
Het |
Ubl7 |
T |
C |
9: 57,821,905 (GRCm39) |
S85P |
probably damaging |
Het |
Urb1 |
C |
A |
16: 90,571,656 (GRCm39) |
S1051I |
probably damaging |
Het |
Usp17le |
A |
G |
7: 104,418,084 (GRCm39) |
W353R |
probably damaging |
Het |
Usp44 |
T |
C |
10: 93,682,330 (GRCm39) |
L260S |
probably benign |
Het |
Wsb1 |
T |
A |
11: 79,131,623 (GRCm39) |
|
probably null |
Het |
Xrcc2 |
A |
T |
5: 25,897,755 (GRCm39) |
C65S |
probably damaging |
Het |
Zfp316 |
T |
A |
5: 143,240,430 (GRCm39) |
M530L |
probably benign |
Het |
Zfp473 |
T |
C |
7: 44,382,563 (GRCm39) |
H590R |
probably damaging |
Het |
Zfp983 |
T |
A |
17: 21,880,850 (GRCm39) |
H259Q |
probably damaging |
Het |
|
Other mutations in Fry |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00327:Fry
|
APN |
5 |
150,263,869 (GRCm39) |
nonsense |
probably null |
|
IGL00328:Fry
|
APN |
5 |
150,263,869 (GRCm39) |
nonsense |
probably null |
|
IGL00841:Fry
|
APN |
5 |
150,346,189 (GRCm39) |
missense |
probably benign |
|
IGL00938:Fry
|
APN |
5 |
150,293,645 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01015:Fry
|
APN |
5 |
150,346,252 (GRCm39) |
missense |
probably benign |
0.18 |
IGL01401:Fry
|
APN |
5 |
150,362,253 (GRCm39) |
missense |
probably benign |
|
IGL01616:Fry
|
APN |
5 |
150,323,064 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01616:Fry
|
APN |
5 |
150,362,276 (GRCm39) |
splice site |
probably null |
|
IGL01748:Fry
|
APN |
5 |
150,269,116 (GRCm39) |
splice site |
probably benign |
|
IGL01965:Fry
|
APN |
5 |
150,305,086 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02030:Fry
|
APN |
5 |
150,395,083 (GRCm39) |
splice site |
probably benign |
|
IGL02079:Fry
|
APN |
5 |
150,323,089 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02087:Fry
|
APN |
5 |
150,327,059 (GRCm39) |
missense |
probably benign |
0.23 |
IGL02113:Fry
|
APN |
5 |
150,323,070 (GRCm39) |
missense |
probably benign |
|
IGL02209:Fry
|
APN |
5 |
150,360,491 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02250:Fry
|
APN |
5 |
150,326,899 (GRCm39) |
splice site |
probably benign |
|
IGL02265:Fry
|
APN |
5 |
150,360,618 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02486:Fry
|
APN |
5 |
150,414,642 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02552:Fry
|
APN |
5 |
150,304,375 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02881:Fry
|
APN |
5 |
150,282,516 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03008:Fry
|
APN |
5 |
150,269,021 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL03140:Fry
|
APN |
5 |
150,419,166 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03171:Fry
|
APN |
5 |
150,304,274 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03389:Fry
|
APN |
5 |
150,317,696 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03404:Fry
|
APN |
5 |
150,249,633 (GRCm39) |
missense |
probably damaging |
1.00 |
Brook
|
UTSW |
5 |
150,249,597 (GRCm39) |
missense |
probably damaging |
1.00 |
haydn
|
UTSW |
5 |
150,341,929 (GRCm39) |
missense |
possibly damaging |
0.94 |
miracle
|
UTSW |
5 |
150,360,624 (GRCm39) |
missense |
probably damaging |
0.99 |
quickening
|
UTSW |
5 |
150,358,241 (GRCm39) |
missense |
probably damaging |
1.00 |
seasons
|
UTSW |
5 |
150,389,902 (GRCm39) |
missense |
probably benign |
0.06 |
Vivaldi
|
UTSW |
5 |
150,317,603 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0023:Fry
|
UTSW |
5 |
150,374,563 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0024:Fry
|
UTSW |
5 |
150,304,268 (GRCm39) |
missense |
probably benign |
0.03 |
R0030:Fry
|
UTSW |
5 |
150,296,034 (GRCm39) |
nonsense |
probably null |
|
R0053:Fry
|
UTSW |
5 |
150,384,842 (GRCm39) |
splice site |
probably benign |
|
R0089:Fry
|
UTSW |
5 |
150,263,892 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0212:Fry
|
UTSW |
5 |
150,419,862 (GRCm39) |
missense |
probably damaging |
0.99 |
R0241:Fry
|
UTSW |
5 |
150,183,811 (GRCm39) |
intron |
probably benign |
|
R0265:Fry
|
UTSW |
5 |
150,358,241 (GRCm39) |
missense |
probably damaging |
1.00 |
R0317:Fry
|
UTSW |
5 |
150,394,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R0532:Fry
|
UTSW |
5 |
150,402,226 (GRCm39) |
splice site |
probably benign |
|
R0532:Fry
|
UTSW |
5 |
150,357,172 (GRCm39) |
unclassified |
probably benign |
|
R0599:Fry
|
UTSW |
5 |
150,360,624 (GRCm39) |
missense |
probably damaging |
0.99 |
R0631:Fry
|
UTSW |
5 |
150,419,817 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0723:Fry
|
UTSW |
5 |
150,419,825 (GRCm39) |
missense |
probably damaging |
1.00 |
R0766:Fry
|
UTSW |
5 |
150,326,897 (GRCm39) |
splice site |
probably benign |
|
R0790:Fry
|
UTSW |
5 |
150,389,902 (GRCm39) |
missense |
probably benign |
0.06 |
R0928:Fry
|
UTSW |
5 |
150,360,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R1104:Fry
|
UTSW |
5 |
150,419,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R1144:Fry
|
UTSW |
5 |
150,341,929 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1172:Fry
|
UTSW |
5 |
150,404,959 (GRCm39) |
nonsense |
probably null |
|
R1312:Fry
|
UTSW |
5 |
150,326,897 (GRCm39) |
splice site |
probably benign |
|
R1347:Fry
|
UTSW |
5 |
150,419,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R1347:Fry
|
UTSW |
5 |
150,419,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R1437:Fry
|
UTSW |
5 |
150,233,890 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1458:Fry
|
UTSW |
5 |
150,304,324 (GRCm39) |
missense |
probably damaging |
1.00 |
R1542:Fry
|
UTSW |
5 |
150,328,431 (GRCm39) |
missense |
probably benign |
0.13 |
R1692:Fry
|
UTSW |
5 |
150,293,692 (GRCm39) |
missense |
probably damaging |
1.00 |
R1826:Fry
|
UTSW |
5 |
150,360,174 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1874:Fry
|
UTSW |
5 |
150,269,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R1875:Fry
|
UTSW |
5 |
150,249,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R1881:Fry
|
UTSW |
5 |
150,401,511 (GRCm39) |
missense |
probably damaging |
0.97 |
R1884:Fry
|
UTSW |
5 |
150,326,985 (GRCm39) |
missense |
probably benign |
0.00 |
R1929:Fry
|
UTSW |
5 |
150,324,389 (GRCm39) |
missense |
probably null |
0.02 |
R2066:Fry
|
UTSW |
5 |
150,293,584 (GRCm39) |
splice site |
probably benign |
|
R2270:Fry
|
UTSW |
5 |
150,324,389 (GRCm39) |
missense |
probably null |
0.02 |
R2356:Fry
|
UTSW |
5 |
150,394,897 (GRCm39) |
missense |
probably benign |
|
R3720:Fry
|
UTSW |
5 |
150,378,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R3773:Fry
|
UTSW |
5 |
150,321,663 (GRCm39) |
missense |
probably damaging |
0.96 |
R3824:Fry
|
UTSW |
5 |
150,419,884 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3902:Fry
|
UTSW |
5 |
150,269,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R3923:Fry
|
UTSW |
5 |
150,336,814 (GRCm39) |
missense |
probably benign |
|
R4250:Fry
|
UTSW |
5 |
150,233,825 (GRCm39) |
missense |
probably damaging |
0.99 |
R4332:Fry
|
UTSW |
5 |
150,305,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R4495:Fry
|
UTSW |
5 |
150,233,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R4610:Fry
|
UTSW |
5 |
150,309,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R4682:Fry
|
UTSW |
5 |
150,346,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R4732:Fry
|
UTSW |
5 |
150,309,472 (GRCm39) |
missense |
|
|
R4733:Fry
|
UTSW |
5 |
150,309,472 (GRCm39) |
missense |
|
|
R4755:Fry
|
UTSW |
5 |
150,321,719 (GRCm39) |
missense |
probably damaging |
0.99 |
R4788:Fry
|
UTSW |
5 |
150,323,101 (GRCm39) |
missense |
probably benign |
0.00 |
R4803:Fry
|
UTSW |
5 |
150,322,998 (GRCm39) |
missense |
probably benign |
0.31 |
R4858:Fry
|
UTSW |
5 |
150,325,108 (GRCm39) |
missense |
possibly damaging |
0.78 |
R4872:Fry
|
UTSW |
5 |
150,317,704 (GRCm39) |
critical splice donor site |
probably null |
|
R4902:Fry
|
UTSW |
5 |
150,419,168 (GRCm39) |
missense |
probably benign |
0.43 |
R4915:Fry
|
UTSW |
5 |
150,402,328 (GRCm39) |
missense |
probably benign |
0.30 |
R4938:Fry
|
UTSW |
5 |
150,401,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R4983:Fry
|
UTSW |
5 |
150,321,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R5004:Fry
|
UTSW |
5 |
150,357,069 (GRCm39) |
missense |
probably benign |
0.16 |
R5040:Fry
|
UTSW |
5 |
150,312,319 (GRCm39) |
missense |
probably damaging |
0.99 |
R5145:Fry
|
UTSW |
5 |
150,293,689 (GRCm39) |
missense |
probably damaging |
0.98 |
R5170:Fry
|
UTSW |
5 |
150,353,319 (GRCm39) |
missense |
probably benign |
0.03 |
R5233:Fry
|
UTSW |
5 |
150,393,185 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5428:Fry
|
UTSW |
5 |
150,328,824 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5468:Fry
|
UTSW |
5 |
150,323,053 (GRCm39) |
missense |
probably benign |
0.44 |
R5481:Fry
|
UTSW |
5 |
150,183,784 (GRCm39) |
missense |
probably benign |
0.01 |
R5494:Fry
|
UTSW |
5 |
150,314,132 (GRCm39) |
missense |
probably damaging |
1.00 |
R5538:Fry
|
UTSW |
5 |
150,419,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R5638:Fry
|
UTSW |
5 |
150,282,546 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5645:Fry
|
UTSW |
5 |
150,304,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R5716:Fry
|
UTSW |
5 |
150,293,686 (GRCm39) |
nonsense |
probably null |
|
R5812:Fry
|
UTSW |
5 |
150,323,136 (GRCm39) |
missense |
probably damaging |
0.99 |
R5813:Fry
|
UTSW |
5 |
150,323,136 (GRCm39) |
missense |
probably damaging |
0.99 |
R5873:Fry
|
UTSW |
5 |
150,302,350 (GRCm39) |
missense |
probably damaging |
1.00 |
R5933:Fry
|
UTSW |
5 |
150,314,265 (GRCm39) |
intron |
probably benign |
|
R6037:Fry
|
UTSW |
5 |
150,351,644 (GRCm39) |
missense |
probably benign |
0.03 |
R6037:Fry
|
UTSW |
5 |
150,351,644 (GRCm39) |
missense |
probably benign |
0.03 |
R6158:Fry
|
UTSW |
5 |
150,378,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R6178:Fry
|
UTSW |
5 |
150,377,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R6481:Fry
|
UTSW |
5 |
150,309,479 (GRCm39) |
missense |
probably damaging |
1.00 |
R6562:Fry
|
UTSW |
5 |
150,249,614 (GRCm39) |
missense |
probably damaging |
1.00 |
R6676:Fry
|
UTSW |
5 |
150,304,387 (GRCm39) |
missense |
probably benign |
0.22 |
R6717:Fry
|
UTSW |
5 |
150,419,777 (GRCm39) |
missense |
probably benign |
0.00 |
R6828:Fry
|
UTSW |
5 |
150,389,911 (GRCm39) |
splice site |
probably null |
|
R6874:Fry
|
UTSW |
5 |
150,360,768 (GRCm39) |
missense |
probably benign |
0.00 |
R6930:Fry
|
UTSW |
5 |
150,351,695 (GRCm39) |
missense |
probably benign |
0.00 |
R6963:Fry
|
UTSW |
5 |
150,381,309 (GRCm39) |
missense |
probably benign |
0.17 |
R6965:Fry
|
UTSW |
5 |
150,339,685 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7051:Fry
|
UTSW |
5 |
150,318,634 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7085:Fry
|
UTSW |
5 |
150,362,214 (GRCm39) |
missense |
probably benign |
0.02 |
R7108:Fry
|
UTSW |
5 |
150,414,555 (GRCm39) |
missense |
|
|
R7108:Fry
|
UTSW |
5 |
150,319,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R7115:Fry
|
UTSW |
5 |
150,309,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R7116:Fry
|
UTSW |
5 |
150,319,334 (GRCm39) |
critical splice donor site |
probably null |
|
R7197:Fry
|
UTSW |
5 |
150,393,232 (GRCm39) |
missense |
|
|
R7256:Fry
|
UTSW |
5 |
150,390,251 (GRCm39) |
missense |
|
|
R7318:Fry
|
UTSW |
5 |
150,360,458 (GRCm39) |
missense |
probably damaging |
0.98 |
R7323:Fry
|
UTSW |
5 |
150,419,814 (GRCm39) |
missense |
|
|
R7358:Fry
|
UTSW |
5 |
150,339,788 (GRCm39) |
missense |
probably benign |
|
R7395:Fry
|
UTSW |
5 |
150,304,348 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7487:Fry
|
UTSW |
5 |
150,338,039 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7491:Fry
|
UTSW |
5 |
150,389,791 (GRCm39) |
missense |
|
|
R7574:Fry
|
UTSW |
5 |
150,304,359 (GRCm39) |
missense |
probably benign |
0.00 |
R7582:Fry
|
UTSW |
5 |
150,419,847 (GRCm39) |
missense |
|
|
R7586:Fry
|
UTSW |
5 |
150,349,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R7650:Fry
|
UTSW |
5 |
150,336,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R7699:Fry
|
UTSW |
5 |
150,328,792 (GRCm39) |
missense |
probably damaging |
0.98 |
R7700:Fry
|
UTSW |
5 |
150,328,792 (GRCm39) |
missense |
probably damaging |
0.98 |
R7972:Fry
|
UTSW |
5 |
150,233,861 (GRCm39) |
missense |
probably benign |
0.05 |
R8058:Fry
|
UTSW |
5 |
150,419,232 (GRCm39) |
missense |
|
|
R8070:Fry
|
UTSW |
5 |
150,401,472 (GRCm39) |
missense |
|
|
R8159:Fry
|
UTSW |
5 |
150,322,998 (GRCm39) |
missense |
probably benign |
0.31 |
R8202:Fry
|
UTSW |
5 |
150,355,202 (GRCm39) |
missense |
probably damaging |
1.00 |
R8261:Fry
|
UTSW |
5 |
150,369,372 (GRCm39) |
missense |
probably damaging |
1.00 |
R8279:Fry
|
UTSW |
5 |
150,419,726 (GRCm39) |
missense |
|
|
R8338:Fry
|
UTSW |
5 |
150,282,516 (GRCm39) |
missense |
probably damaging |
0.99 |
R8370:Fry
|
UTSW |
5 |
150,319,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R8673:Fry
|
UTSW |
5 |
150,318,576 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8786:Fry
|
UTSW |
5 |
150,317,501 (GRCm39) |
missense |
probably benign |
0.00 |
R8815:Fry
|
UTSW |
5 |
150,317,603 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8847:Fry
|
UTSW |
5 |
150,309,472 (GRCm39) |
missense |
|
|
R9023:Fry
|
UTSW |
5 |
150,360,768 (GRCm39) |
missense |
probably benign |
0.00 |
R9025:Fry
|
UTSW |
5 |
150,219,273 (GRCm39) |
intron |
probably benign |
|
R9125:Fry
|
UTSW |
5 |
150,269,525 (GRCm39) |
missense |
probably damaging |
0.97 |
R9172:Fry
|
UTSW |
5 |
150,336,793 (GRCm39) |
missense |
probably benign |
|
R9262:Fry
|
UTSW |
5 |
150,305,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R9263:Fry
|
UTSW |
5 |
150,322,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R9293:Fry
|
UTSW |
5 |
150,419,297 (GRCm39) |
missense |
|
|
R9368:Fry
|
UTSW |
5 |
150,401,403 (GRCm39) |
missense |
|
|
R9401:Fry
|
UTSW |
5 |
150,302,403 (GRCm39) |
missense |
probably damaging |
1.00 |
R9402:Fry
|
UTSW |
5 |
150,360,318 (GRCm39) |
missense |
probably damaging |
1.00 |
R9402:Fry
|
UTSW |
5 |
150,357,161 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9420:Fry
|
UTSW |
5 |
150,356,994 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9557:Fry
|
UTSW |
5 |
150,389,781 (GRCm39) |
missense |
|
|
R9647:Fry
|
UTSW |
5 |
150,292,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R9650:Fry
|
UTSW |
5 |
150,369,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R9655:Fry
|
UTSW |
5 |
150,362,251 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9664:Fry
|
UTSW |
5 |
150,282,488 (GRCm39) |
missense |
probably damaging |
0.98 |
R9668:Fry
|
UTSW |
5 |
150,282,318 (GRCm39) |
missense |
probably damaging |
1.00 |
R9732:Fry
|
UTSW |
5 |
150,328,758 (GRCm39) |
missense |
probably benign |
0.00 |
R9773:Fry
|
UTSW |
5 |
150,322,728 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Fry
|
UTSW |
5 |
150,233,902 (GRCm39) |
missense |
possibly damaging |
0.80 |
|