Other mutations in this stock |
Total: 98 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4833420G17Rik |
T |
C |
13: 119,606,478 (GRCm39) |
V240A |
probably damaging |
Het |
A930009A15Rik |
C |
T |
10: 115,406,019 (GRCm39) |
|
probably benign |
Het |
Aarsd1 |
A |
G |
11: 101,301,970 (GRCm39) |
I201T |
probably damaging |
Het |
Acaca |
T |
A |
11: 84,152,414 (GRCm39) |
Y854N |
probably benign |
Het |
Adra2c |
T |
C |
5: 35,437,759 (GRCm39) |
L177P |
probably damaging |
Het |
Akr1c12 |
A |
T |
13: 4,329,309 (GRCm39) |
I16N |
probably damaging |
Het |
Aldh8a1 |
A |
T |
10: 21,256,729 (GRCm39) |
I47F |
possibly damaging |
Het |
Birc6 |
A |
G |
17: 74,886,879 (GRCm39) |
I736V |
probably benign |
Het |
Bmp2 |
A |
T |
2: 133,402,817 (GRCm39) |
M123L |
probably benign |
Het |
C1ql1 |
T |
C |
11: 102,836,812 (GRCm39) |
Y159C |
probably damaging |
Het |
Ccdc148 |
T |
C |
2: 58,713,645 (GRCm39) |
Y502C |
probably damaging |
Het |
Ccdc168 |
A |
T |
1: 44,098,593 (GRCm39) |
V835E |
possibly damaging |
Het |
Cenpf |
A |
T |
1: 189,390,864 (GRCm39) |
N989K |
probably damaging |
Het |
Ciz1 |
A |
G |
2: 32,257,380 (GRCm39) |
M142V |
probably benign |
Het |
Cnot4 |
T |
C |
6: 35,029,939 (GRCm39) |
R320G |
possibly damaging |
Het |
Cyth1 |
G |
T |
11: 118,073,689 (GRCm39) |
H215N |
probably damaging |
Het |
Dapk1 |
G |
A |
13: 60,908,987 (GRCm39) |
G1200D |
probably damaging |
Het |
Dhps |
A |
G |
8: 85,799,181 (GRCm39) |
Y103C |
probably damaging |
Het |
Dnah1 |
T |
A |
14: 31,041,865 (GRCm39) |
E35D |
probably benign |
Het |
Dnajb9 |
A |
T |
12: 44,254,169 (GRCm39) |
D79E |
probably damaging |
Het |
Eif4a2 |
T |
C |
16: 22,928,877 (GRCm39) |
F164S |
probably benign |
Het |
Enpp2 |
T |
C |
15: 54,714,813 (GRCm39) |
T595A |
probably benign |
Het |
Exoc6b |
T |
A |
6: 84,768,366 (GRCm39) |
|
probably null |
Het |
Fam171a1 |
T |
C |
2: 3,221,391 (GRCm39) |
S286P |
probably damaging |
Het |
Fermt2 |
T |
A |
14: 45,706,782 (GRCm39) |
N338I |
probably damaging |
Het |
Fhdc1 |
A |
G |
3: 84,353,438 (GRCm39) |
F596L |
probably benign |
Het |
Fry |
T |
C |
5: 150,304,359 (GRCm39) |
V583A |
probably benign |
Het |
Gbp10 |
G |
A |
5: 105,384,015 (GRCm39) |
|
probably benign |
Het |
Gdap1 |
T |
A |
1: 17,231,665 (GRCm39) |
F337I |
possibly damaging |
Het |
Git2 |
C |
T |
5: 114,904,550 (GRCm39) |
R123H |
probably damaging |
Het |
Gpr6 |
A |
T |
10: 40,946,652 (GRCm39) |
I310N |
possibly damaging |
Het |
Gpsm2 |
G |
A |
3: 108,608,061 (GRCm39) |
A239V |
probably damaging |
Het |
Hexa |
T |
C |
9: 59,471,267 (GRCm39) |
V507A |
probably benign |
Het |
Hmcn2 |
A |
T |
2: 31,345,531 (GRCm39) |
H4718L |
possibly damaging |
Het |
Hrh4 |
T |
C |
18: 13,154,970 (GRCm39) |
F170L |
possibly damaging |
Het |
Ica1 |
T |
C |
6: 8,658,266 (GRCm39) |
T284A |
probably benign |
Het |
Itga5 |
T |
C |
15: 103,258,876 (GRCm39) |
N774S |
probably damaging |
Het |
Itgb2 |
T |
C |
10: 77,395,992 (GRCm39) |
S556P |
probably benign |
Het |
Kash5 |
A |
T |
7: 44,854,035 (GRCm39) |
H31Q |
possibly damaging |
Het |
Kcnq4 |
A |
G |
4: 120,568,565 (GRCm39) |
F384L |
probably benign |
Het |
Lama2 |
A |
T |
10: 26,882,726 (GRCm39) |
N2612K |
probably benign |
Het |
Lnx1 |
T |
C |
5: 74,846,099 (GRCm39) |
E117G |
probably benign |
Het |
Lrrc14b |
G |
T |
13: 74,508,892 (GRCm39) |
A505E |
probably damaging |
Het |
Ly6g |
T |
C |
15: 75,030,413 (GRCm39) |
I77T |
probably benign |
Het |
Mmp1a |
TG |
TGG |
9: 7,465,083 (GRCm38) |
|
probably null |
Het |
Mrgpre |
C |
T |
7: 143,335,087 (GRCm39) |
V139M |
probably damaging |
Het |
Muc4 |
T |
A |
16: 32,753,411 (GRCm38) |
S1096T |
probably benign |
Het |
Myrfl |
G |
A |
10: 116,667,430 (GRCm39) |
R337* |
probably null |
Het |
Ndufa4 |
C |
T |
6: 11,906,092 (GRCm39) |
V20I |
probably benign |
Het |
Nf1 |
A |
G |
11: 79,299,595 (GRCm39) |
D241G |
probably null |
Het |
Nid1 |
A |
G |
13: 13,643,028 (GRCm39) |
D322G |
probably benign |
Het |
Nova1 |
A |
T |
12: 46,747,544 (GRCm39) |
D244E |
unknown |
Het |
Or11g27 |
T |
A |
14: 50,771,770 (GRCm39) |
D300E |
probably benign |
Het |
Or4a68 |
T |
C |
2: 89,269,745 (GRCm39) |
K293E |
possibly damaging |
Het |
Or5m10b |
A |
G |
2: 85,699,350 (GRCm39) |
K138R |
probably benign |
Het |
Padi2 |
C |
A |
4: 140,676,648 (GRCm39) |
N595K |
possibly damaging |
Het |
Pag1 |
A |
G |
3: 9,758,951 (GRCm39) |
I389T |
probably damaging |
Het |
Pcdh10 |
G |
T |
3: 45,335,810 (GRCm39) |
G708V |
possibly damaging |
Het |
Pecam1 |
A |
G |
11: 106,590,610 (GRCm39) |
S55P |
probably damaging |
Het |
Plin3 |
A |
T |
17: 56,591,192 (GRCm39) |
V196E |
possibly damaging |
Het |
Plxdc1 |
A |
T |
11: 97,847,316 (GRCm39) |
L119Q |
possibly damaging |
Het |
Pnliprp1 |
A |
T |
19: 58,726,681 (GRCm39) |
N346I |
probably damaging |
Het |
Ppp1r27 |
A |
T |
11: 120,441,856 (GRCm39) |
Y8* |
probably null |
Het |
Prg3 |
A |
T |
2: 84,819,746 (GRCm39) |
D80V |
probably damaging |
Het |
Prmt5 |
T |
C |
14: 54,745,347 (GRCm39) |
N607D |
possibly damaging |
Het |
Ptprs |
A |
G |
17: 56,730,538 (GRCm39) |
F1144L |
probably benign |
Het |
Rai14 |
C |
T |
15: 10,593,189 (GRCm39) |
G152R |
probably damaging |
Het |
Rap1gds1 |
T |
A |
3: 138,661,976 (GRCm39) |
R427* |
probably null |
Het |
Recql5 |
A |
G |
11: 115,819,248 (GRCm39) |
V106A |
probably benign |
Het |
Resp18 |
T |
C |
1: 75,250,615 (GRCm39) |
T155A |
probably benign |
Het |
Rfx6 |
A |
G |
10: 51,557,914 (GRCm39) |
D129G |
probably benign |
Het |
Rsf1 |
T |
A |
7: 97,310,374 (GRCm39) |
I368K |
|
Het |
Sema6a |
C |
G |
18: 47,424,231 (GRCm39) |
V226L |
probably damaging |
Het |
Sf1 |
A |
G |
19: 6,422,234 (GRCm39) |
E220G |
probably damaging |
Het |
Shld2 |
C |
T |
14: 33,959,423 (GRCm39) |
S853N |
probably damaging |
Het |
Sidt1 |
T |
A |
16: 44,079,848 (GRCm39) |
Y602F |
probably damaging |
Het |
Slc17a8 |
A |
G |
10: 89,428,008 (GRCm39) |
I273T |
probably benign |
Het |
Slc28a2b |
A |
T |
2: 122,353,325 (GRCm39) |
I502F |
not run |
Het |
Slc41a1 |
A |
T |
1: 131,766,889 (GRCm39) |
I136F |
probably damaging |
Het |
Snrpb |
T |
C |
2: 130,018,939 (GRCm39) |
I51V |
probably benign |
Het |
Sprr2f |
T |
A |
3: 92,273,254 (GRCm39) |
C18S |
unknown |
Het |
Svil |
C |
A |
18: 5,095,188 (GRCm39) |
T1457K |
probably benign |
Het |
Syt1 |
A |
T |
10: 108,340,262 (GRCm39) |
I352N |
probably damaging |
Het |
Tas2r119 |
A |
G |
15: 32,178,279 (GRCm39) |
K282E |
probably damaging |
Het |
Timeless |
T |
C |
10: 128,080,538 (GRCm39) |
F473S |
probably damaging |
Het |
Tmc3 |
A |
G |
7: 83,247,481 (GRCm39) |
D192G |
probably damaging |
Het |
Trmt1l |
T |
A |
1: 151,316,591 (GRCm39) |
I184N |
possibly damaging |
Het |
Ttll6 |
G |
A |
11: 96,025,701 (GRCm39) |
V61M |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,632,755 (GRCm39) |
E14100K |
probably damaging |
Het |
Txndc2 |
T |
A |
17: 65,945,620 (GRCm39) |
I186F |
possibly damaging |
Het |
Ubr1 |
A |
T |
2: 120,703,672 (GRCm39) |
S1553T |
possibly damaging |
Het |
Vmn1r208 |
T |
C |
13: 22,956,705 (GRCm39) |
N264S |
probably benign |
Het |
Vmn1r87 |
T |
A |
7: 12,865,613 (GRCm39) |
M225L |
probably benign |
Het |
Vmn2r101 |
T |
A |
17: 19,831,899 (GRCm39) |
C632S |
possibly damaging |
Het |
Wdr97 |
T |
A |
15: 76,241,949 (GRCm39) |
Y747* |
probably null |
Het |
Zfp474 |
T |
C |
18: 52,772,261 (GRCm39) |
S305P |
probably benign |
Het |
Zfp59 |
A |
G |
7: 27,552,863 (GRCm39) |
N105S |
probably benign |
Het |
Zfp804b |
T |
A |
5: 6,822,301 (GRCm39) |
Y254F |
possibly damaging |
Het |
|
Other mutations in Stab1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00087:Stab1
|
APN |
14 |
30,883,314 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00323:Stab1
|
APN |
14 |
30,861,263 (GRCm39) |
missense |
probably benign |
0.04 |
IGL00515:Stab1
|
APN |
14 |
30,881,686 (GRCm39) |
missense |
probably benign |
0.20 |
IGL00844:Stab1
|
APN |
14 |
30,869,023 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01374:Stab1
|
APN |
14 |
30,869,032 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01384:Stab1
|
APN |
14 |
30,872,365 (GRCm39) |
missense |
probably benign |
|
IGL01431:Stab1
|
APN |
14 |
30,870,952 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01787:Stab1
|
APN |
14 |
30,861,765 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02128:Stab1
|
APN |
14 |
30,872,398 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02138:Stab1
|
APN |
14 |
30,865,470 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02256:Stab1
|
APN |
14 |
30,863,549 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02340:Stab1
|
APN |
14 |
30,862,367 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02507:Stab1
|
APN |
14 |
30,861,167 (GRCm39) |
unclassified |
probably benign |
|
IGL02695:Stab1
|
APN |
14 |
30,881,228 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02755:Stab1
|
APN |
14 |
30,861,595 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02870:Stab1
|
APN |
14 |
30,861,354 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02884:Stab1
|
APN |
14 |
30,872,100 (GRCm39) |
splice site |
probably null |
|
IGL03035:Stab1
|
APN |
14 |
30,869,726 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03267:Stab1
|
APN |
14 |
30,864,686 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03286:Stab1
|
APN |
14 |
30,881,283 (GRCm39) |
splice site |
probably benign |
|
IGL03366:Stab1
|
APN |
14 |
30,872,220 (GRCm39) |
missense |
possibly damaging |
0.58 |
IGL03412:Stab1
|
APN |
14 |
30,876,364 (GRCm39) |
missense |
probably benign |
0.42 |
R0906_Stab1_335
|
UTSW |
14 |
30,867,206 (GRCm39) |
missense |
probably benign |
0.19 |
R5086_Stab1_467
|
UTSW |
14 |
30,881,261 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02835:Stab1
|
UTSW |
14 |
30,867,981 (GRCm39) |
critical splice donor site |
probably null |
|
K7371:Stab1
|
UTSW |
14 |
30,872,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R0053:Stab1
|
UTSW |
14 |
30,862,644 (GRCm39) |
missense |
possibly damaging |
0.57 |
R0053:Stab1
|
UTSW |
14 |
30,862,644 (GRCm39) |
missense |
possibly damaging |
0.57 |
R0066:Stab1
|
UTSW |
14 |
30,879,027 (GRCm39) |
splice site |
probably benign |
|
R0066:Stab1
|
UTSW |
14 |
30,879,027 (GRCm39) |
splice site |
probably benign |
|
R0363:Stab1
|
UTSW |
14 |
30,880,965 (GRCm39) |
splice site |
probably benign |
|
R0387:Stab1
|
UTSW |
14 |
30,870,058 (GRCm39) |
missense |
probably benign |
0.00 |
R0391:Stab1
|
UTSW |
14 |
30,865,375 (GRCm39) |
missense |
probably benign |
0.21 |
R0513:Stab1
|
UTSW |
14 |
30,870,902 (GRCm39) |
missense |
probably benign |
0.08 |
R0546:Stab1
|
UTSW |
14 |
30,861,507 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0825:Stab1
|
UTSW |
14 |
30,874,557 (GRCm39) |
missense |
probably benign |
0.16 |
R0906:Stab1
|
UTSW |
14 |
30,867,206 (GRCm39) |
missense |
probably benign |
0.19 |
R0963:Stab1
|
UTSW |
14 |
30,869,231 (GRCm39) |
missense |
probably damaging |
0.97 |
R1219:Stab1
|
UTSW |
14 |
30,862,578 (GRCm39) |
splice site |
probably null |
|
R1234:Stab1
|
UTSW |
14 |
30,872,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R1260:Stab1
|
UTSW |
14 |
30,873,846 (GRCm39) |
missense |
probably damaging |
1.00 |
R1400:Stab1
|
UTSW |
14 |
30,861,787 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1405:Stab1
|
UTSW |
14 |
30,870,958 (GRCm39) |
missense |
probably benign |
0.19 |
R1405:Stab1
|
UTSW |
14 |
30,870,958 (GRCm39) |
missense |
probably benign |
0.19 |
R1440:Stab1
|
UTSW |
14 |
30,873,647 (GRCm39) |
nonsense |
probably null |
|
R1472:Stab1
|
UTSW |
14 |
30,863,543 (GRCm39) |
missense |
probably benign |
0.01 |
R1474:Stab1
|
UTSW |
14 |
30,871,818 (GRCm39) |
missense |
probably benign |
0.45 |
R1475:Stab1
|
UTSW |
14 |
30,885,785 (GRCm39) |
missense |
probably benign |
|
R1509:Stab1
|
UTSW |
14 |
30,873,541 (GRCm39) |
splice site |
probably benign |
|
R1551:Stab1
|
UTSW |
14 |
30,882,456 (GRCm39) |
missense |
probably benign |
0.00 |
R1572:Stab1
|
UTSW |
14 |
30,872,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R1633:Stab1
|
UTSW |
14 |
30,872,337 (GRCm39) |
splice site |
probably null |
|
R1719:Stab1
|
UTSW |
14 |
30,867,985 (GRCm39) |
nonsense |
probably null |
|
R1733:Stab1
|
UTSW |
14 |
30,867,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R1763:Stab1
|
UTSW |
14 |
30,890,373 (GRCm39) |
missense |
probably benign |
0.04 |
R1808:Stab1
|
UTSW |
14 |
30,863,101 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1816:Stab1
|
UTSW |
14 |
30,879,422 (GRCm39) |
missense |
probably benign |
0.03 |
R1853:Stab1
|
UTSW |
14 |
30,862,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R1891:Stab1
|
UTSW |
14 |
30,863,287 (GRCm39) |
missense |
probably benign |
0.07 |
R1984:Stab1
|
UTSW |
14 |
30,872,605 (GRCm39) |
missense |
probably benign |
0.20 |
R1998:Stab1
|
UTSW |
14 |
30,884,110 (GRCm39) |
nonsense |
probably null |
|
R2165:Stab1
|
UTSW |
14 |
30,890,392 (GRCm39) |
missense |
probably benign |
0.20 |
R2191:Stab1
|
UTSW |
14 |
30,881,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R2191:Stab1
|
UTSW |
14 |
30,864,757 (GRCm39) |
missense |
probably benign |
0.03 |
R2233:Stab1
|
UTSW |
14 |
30,883,837 (GRCm39) |
missense |
probably benign |
0.08 |
R2303:Stab1
|
UTSW |
14 |
30,868,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R2496:Stab1
|
UTSW |
14 |
30,883,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R2504:Stab1
|
UTSW |
14 |
30,884,997 (GRCm39) |
critical splice donor site |
probably null |
|
R2519:Stab1
|
UTSW |
14 |
30,876,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R2926:Stab1
|
UTSW |
14 |
30,883,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R4025:Stab1
|
UTSW |
14 |
30,876,909 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4113:Stab1
|
UTSW |
14 |
30,890,436 (GRCm39) |
missense |
probably damaging |
0.98 |
R4258:Stab1
|
UTSW |
14 |
30,876,629 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4588:Stab1
|
UTSW |
14 |
30,879,402 (GRCm39) |
missense |
probably benign |
0.01 |
R4644:Stab1
|
UTSW |
14 |
30,862,444 (GRCm39) |
unclassified |
probably benign |
|
R4660:Stab1
|
UTSW |
14 |
30,876,872 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4801:Stab1
|
UTSW |
14 |
30,863,328 (GRCm39) |
nonsense |
probably null |
|
R4802:Stab1
|
UTSW |
14 |
30,863,328 (GRCm39) |
nonsense |
probably null |
|
R4870:Stab1
|
UTSW |
14 |
30,864,000 (GRCm39) |
missense |
probably benign |
0.13 |
R4872:Stab1
|
UTSW |
14 |
30,862,350 (GRCm39) |
missense |
probably damaging |
1.00 |
R4881:Stab1
|
UTSW |
14 |
30,865,629 (GRCm39) |
missense |
probably benign |
0.32 |
R4941:Stab1
|
UTSW |
14 |
30,873,528 (GRCm39) |
missense |
probably benign |
0.00 |
R5061:Stab1
|
UTSW |
14 |
30,885,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R5086:Stab1
|
UTSW |
14 |
30,881,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R5086:Stab1
|
UTSW |
14 |
30,865,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R5087:Stab1
|
UTSW |
14 |
30,881,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R5092:Stab1
|
UTSW |
14 |
30,867,812 (GRCm39) |
missense |
probably benign |
0.01 |
R5102:Stab1
|
UTSW |
14 |
30,869,974 (GRCm39) |
critical splice donor site |
probably null |
|
R5107:Stab1
|
UTSW |
14 |
30,885,752 (GRCm39) |
splice site |
probably null |
|
R5195:Stab1
|
UTSW |
14 |
30,862,478 (GRCm39) |
unclassified |
probably benign |
|
R5217:Stab1
|
UTSW |
14 |
30,881,476 (GRCm39) |
missense |
probably benign |
0.25 |
R5285:Stab1
|
UTSW |
14 |
30,865,433 (GRCm39) |
unclassified |
probably benign |
|
R5327:Stab1
|
UTSW |
14 |
30,883,793 (GRCm39) |
nonsense |
probably null |
|
R5647:Stab1
|
UTSW |
14 |
30,879,397 (GRCm39) |
nonsense |
probably null |
|
R5696:Stab1
|
UTSW |
14 |
30,882,178 (GRCm39) |
missense |
probably benign |
|
R5996:Stab1
|
UTSW |
14 |
30,861,508 (GRCm39) |
missense |
probably benign |
0.39 |
R6016:Stab1
|
UTSW |
14 |
30,880,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R6017:Stab1
|
UTSW |
14 |
30,863,501 (GRCm39) |
missense |
probably benign |
0.00 |
R6174:Stab1
|
UTSW |
14 |
30,884,476 (GRCm39) |
nonsense |
probably null |
|
R6366:Stab1
|
UTSW |
14 |
30,863,395 (GRCm39) |
missense |
probably benign |
0.10 |
R6754:Stab1
|
UTSW |
14 |
30,863,038 (GRCm39) |
missense |
probably benign |
|
R6788:Stab1
|
UTSW |
14 |
30,861,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R6898:Stab1
|
UTSW |
14 |
30,880,920 (GRCm39) |
missense |
probably benign |
0.00 |
R7124:Stab1
|
UTSW |
14 |
30,882,824 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7145:Stab1
|
UTSW |
14 |
30,867,030 (GRCm39) |
critical splice donor site |
probably null |
|
R7153:Stab1
|
UTSW |
14 |
30,882,541 (GRCm39) |
missense |
probably benign |
0.16 |
R7213:Stab1
|
UTSW |
14 |
30,865,630 (GRCm39) |
missense |
probably benign |
|
R7215:Stab1
|
UTSW |
14 |
30,882,754 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7319:Stab1
|
UTSW |
14 |
30,862,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R7389:Stab1
|
UTSW |
14 |
30,869,196 (GRCm39) |
missense |
probably benign |
0.00 |
R7400:Stab1
|
UTSW |
14 |
30,879,341 (GRCm39) |
missense |
probably null |
1.00 |
R7427:Stab1
|
UTSW |
14 |
30,881,216 (GRCm39) |
missense |
probably benign |
0.00 |
R7428:Stab1
|
UTSW |
14 |
30,881,216 (GRCm39) |
missense |
probably benign |
0.00 |
R7484:Stab1
|
UTSW |
14 |
30,882,274 (GRCm39) |
missense |
probably benign |
0.00 |
R7568:Stab1
|
UTSW |
14 |
30,874,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R7619:Stab1
|
UTSW |
14 |
30,867,194 (GRCm39) |
missense |
probably benign |
|
R7623:Stab1
|
UTSW |
14 |
30,862,578 (GRCm39) |
missense |
probably benign |
0.03 |
R7721:Stab1
|
UTSW |
14 |
30,863,413 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7869:Stab1
|
UTSW |
14 |
30,876,429 (GRCm39) |
missense |
probably benign |
0.01 |
R7936:Stab1
|
UTSW |
14 |
30,879,372 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7956:Stab1
|
UTSW |
14 |
30,881,981 (GRCm39) |
missense |
probably benign |
0.02 |
R7973:Stab1
|
UTSW |
14 |
30,881,590 (GRCm39) |
critical splice donor site |
probably null |
|
R8059:Stab1
|
UTSW |
14 |
30,882,198 (GRCm39) |
missense |
probably benign |
0.02 |
R8116:Stab1
|
UTSW |
14 |
30,880,910 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8304:Stab1
|
UTSW |
14 |
30,870,911 (GRCm39) |
missense |
probably benign |
0.14 |
R8368:Stab1
|
UTSW |
14 |
30,870,368 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8495:Stab1
|
UTSW |
14 |
30,877,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R8513:Stab1
|
UTSW |
14 |
30,871,747 (GRCm39) |
critical splice donor site |
probably null |
|
R8544:Stab1
|
UTSW |
14 |
30,885,008 (GRCm39) |
nonsense |
probably null |
|
R8671:Stab1
|
UTSW |
14 |
30,879,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R8885:Stab1
|
UTSW |
14 |
30,883,771 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8974:Stab1
|
UTSW |
14 |
30,882,779 (GRCm39) |
missense |
probably benign |
|
R9022:Stab1
|
UTSW |
14 |
30,882,226 (GRCm39) |
missense |
probably benign |
0.01 |
R9059:Stab1
|
UTSW |
14 |
30,876,805 (GRCm39) |
missense |
probably benign |
0.01 |
R9226:Stab1
|
UTSW |
14 |
30,867,812 (GRCm39) |
missense |
probably benign |
0.00 |
R9272:Stab1
|
UTSW |
14 |
30,867,298 (GRCm39) |
missense |
probably benign |
0.05 |
R9388:Stab1
|
UTSW |
14 |
30,876,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R9401:Stab1
|
UTSW |
14 |
30,883,069 (GRCm39) |
missense |
probably benign |
|
R9433:Stab1
|
UTSW |
14 |
30,865,531 (GRCm39) |
missense |
probably benign |
0.00 |
R9450:Stab1
|
UTSW |
14 |
30,884,896 (GRCm39) |
missense |
possibly damaging |
0.62 |
R9505:Stab1
|
UTSW |
14 |
30,877,722 (GRCm39) |
missense |
probably damaging |
1.00 |
R9570:Stab1
|
UTSW |
14 |
30,864,638 (GRCm39) |
missense |
probably benign |
0.01 |
R9624:Stab1
|
UTSW |
14 |
30,863,345 (GRCm39) |
missense |
|
|
R9694:Stab1
|
UTSW |
14 |
30,876,901 (GRCm39) |
missense |
probably benign |
0.06 |
R9723:Stab1
|
UTSW |
14 |
30,885,848 (GRCm39) |
missense |
probably benign |
0.10 |
X0026:Stab1
|
UTSW |
14 |
30,884,148 (GRCm39) |
missense |
possibly damaging |
0.91 |
Z1176:Stab1
|
UTSW |
14 |
30,872,617 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Stab1
|
UTSW |
14 |
30,863,995 (GRCm39) |
missense |
probably benign |
0.00 |
|