Other mutations in this stock |
Total: 103 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700006A11Rik |
T |
G |
3: 124,200,163 (GRCm39) |
L476F |
probably damaging |
Het |
4930432E11Rik |
A |
T |
7: 29,278,591 (GRCm39) |
|
noncoding transcript |
Het |
A930011G23Rik |
A |
T |
5: 99,370,897 (GRCm39) |
|
probably benign |
Het |
Abcd3 |
A |
G |
3: 121,575,612 (GRCm39) |
Y217H |
probably damaging |
Het |
Abraxas1 |
A |
T |
5: 100,965,822 (GRCm39) |
|
probably benign |
Het |
Acsbg1 |
T |
C |
9: 54,523,346 (GRCm39) |
Y427C |
probably damaging |
Het |
Acsbg3 |
T |
A |
17: 57,192,169 (GRCm39) |
Y577* |
probably null |
Het |
Adam10 |
T |
A |
9: 70,683,651 (GRCm39) |
|
probably benign |
Het |
Adam24 |
G |
A |
8: 41,134,004 (GRCm39) |
V491I |
possibly damaging |
Het |
Adamts2 |
T |
G |
11: 50,647,524 (GRCm39) |
V299G |
probably damaging |
Het |
Adh7 |
A |
G |
3: 137,929,752 (GRCm39) |
T143A |
probably damaging |
Het |
Ahcyl1 |
A |
G |
3: 107,581,419 (GRCm39) |
S81P |
probably benign |
Het |
Arhgap20 |
C |
A |
9: 51,761,215 (GRCm39) |
T986K |
probably benign |
Het |
Atp13a5 |
A |
T |
16: 29,133,478 (GRCm39) |
I391N |
possibly damaging |
Het |
Atp6v0a1 |
C |
A |
11: 100,917,511 (GRCm39) |
A143E |
probably benign |
Het |
Calcrl |
A |
G |
2: 84,181,629 (GRCm39) |
I173T |
probably damaging |
Het |
Casz1 |
A |
G |
4: 149,017,394 (GRCm39) |
T228A |
probably benign |
Het |
Cckar |
A |
G |
5: 53,857,321 (GRCm39) |
I292T |
probably damaging |
Het |
Ccn5 |
G |
A |
2: 163,670,906 (GRCm39) |
V138M |
probably damaging |
Het |
Cfhr2 |
T |
A |
1: 139,786,383 (GRCm39) |
|
probably null |
Het |
Chkb |
T |
C |
15: 89,313,260 (GRCm39) |
I109V |
possibly damaging |
Het |
Clec2i |
T |
C |
6: 128,865,069 (GRCm39) |
|
probably null |
Het |
Clec4a4 |
T |
A |
6: 123,000,934 (GRCm39) |
W216R |
probably damaging |
Het |
Cntnap1 |
A |
C |
11: 101,077,337 (GRCm39) |
I1000L |
probably damaging |
Het |
Cp |
C |
A |
3: 20,011,549 (GRCm39) |
D34E |
possibly damaging |
Het |
Cse1l |
T |
C |
2: 166,782,044 (GRCm39) |
|
probably null |
Het |
Dennd3 |
T |
C |
15: 73,394,357 (GRCm39) |
|
probably null |
Het |
Dnah7a |
A |
G |
1: 53,616,382 (GRCm39) |
V1193A |
probably benign |
Het |
Eaf2 |
A |
G |
16: 36,630,832 (GRCm39) |
|
probably null |
Het |
Efcab3 |
T |
A |
11: 104,611,765 (GRCm39) |
S536T |
probably benign |
Het |
Ephb2 |
T |
C |
4: 136,421,136 (GRCm39) |
T405A |
possibly damaging |
Het |
Fam117a |
G |
A |
11: 95,269,779 (GRCm39) |
V348M |
probably damaging |
Het |
Fh1 |
T |
C |
1: 175,428,990 (GRCm39) |
*167W |
probably null |
Het |
Fmo9 |
T |
A |
1: 166,490,868 (GRCm39) |
I486F |
probably benign |
Het |
Gabbr1 |
T |
A |
17: 37,365,771 (GRCm39) |
I150N |
probably damaging |
Het |
Gfpt1 |
T |
C |
6: 87,054,179 (GRCm39) |
V478A |
possibly damaging |
Het |
Gm2663 |
A |
T |
6: 40,974,894 (GRCm39) |
V59E |
probably damaging |
Het |
Gm4868 |
T |
A |
5: 125,925,176 (GRCm39) |
|
noncoding transcript |
Het |
Heatr4 |
T |
A |
12: 84,026,934 (GRCm39) |
T108S |
probably benign |
Het |
Hells |
G |
T |
19: 38,935,286 (GRCm39) |
A319S |
probably benign |
Het |
Helz2 |
A |
G |
2: 180,876,780 (GRCm39) |
V1238A |
probably benign |
Het |
Helz2 |
T |
A |
2: 180,880,252 (GRCm39) |
Q488L |
possibly damaging |
Het |
Hkdc1 |
A |
G |
10: 62,227,162 (GRCm39) |
F765S |
probably damaging |
Het |
Hspg2 |
T |
A |
4: 137,245,820 (GRCm39) |
W938R |
probably damaging |
Het |
Itpr2 |
G |
A |
6: 146,060,399 (GRCm39) |
R2473* |
probably null |
Het |
Kctd1 |
C |
T |
18: 15,194,839 (GRCm39) |
V595I |
probably benign |
Het |
Krt7 |
A |
G |
15: 101,321,290 (GRCm39) |
Y369C |
probably damaging |
Het |
Krt72 |
T |
C |
15: 101,689,364 (GRCm39) |
T323A |
probably benign |
Het |
Krt76 |
A |
G |
15: 101,801,122 (GRCm39) |
L58P |
unknown |
Het |
Liph |
C |
A |
16: 21,786,800 (GRCm39) |
R272L |
probably benign |
Het |
Lrrc9 |
A |
T |
12: 72,502,772 (GRCm39) |
K248* |
probably null |
Het |
Mei4 |
T |
A |
9: 81,809,195 (GRCm39) |
S93T |
probably damaging |
Het |
Mgll |
T |
A |
6: 88,790,930 (GRCm39) |
Y183* |
probably null |
Het |
Myo5b |
A |
G |
18: 74,875,218 (GRCm39) |
M1541V |
probably benign |
Het |
Napg |
A |
G |
18: 63,115,762 (GRCm39) |
E66G |
probably benign |
Het |
Npr3 |
T |
C |
15: 11,851,572 (GRCm39) |
D406G |
probably damaging |
Het |
Nr2c2 |
A |
G |
6: 92,136,224 (GRCm39) |
T355A |
possibly damaging |
Het |
Or13j1 |
G |
A |
4: 43,706,041 (GRCm39) |
H176Y |
probably damaging |
Het |
Or4a71 |
A |
T |
2: 89,357,989 (GRCm39) |
I255K |
probably benign |
Het |
Or51m1 |
G |
T |
7: 103,578,668 (GRCm39) |
V213L |
probably benign |
Het |
Or51v8 |
A |
G |
7: 103,319,845 (GRCm39) |
I131T |
probably benign |
Het |
Or52z13 |
A |
T |
7: 103,247,107 (GRCm39) |
I195F |
probably damaging |
Het |
Or5b107 |
T |
C |
19: 13,142,404 (GRCm39) |
Y9H |
probably benign |
Het |
Or8d1 |
A |
G |
9: 38,766,846 (GRCm39) |
M163V |
possibly damaging |
Het |
Orai2 |
T |
C |
5: 136,179,793 (GRCm39) |
E80G |
probably damaging |
Het |
Pcdhb14 |
T |
A |
18: 37,582,535 (GRCm39) |
V547E |
probably damaging |
Het |
Pcdhb15 |
T |
C |
18: 37,609,084 (GRCm39) |
I772T |
possibly damaging |
Het |
Pdcd6 |
A |
G |
13: 74,453,700 (GRCm39) |
I146T |
probably damaging |
Het |
Phldb2 |
T |
A |
16: 45,621,988 (GRCm39) |
D664V |
probably damaging |
Het |
Pik3ap1 |
A |
T |
19: 41,320,673 (GRCm39) |
V182E |
probably damaging |
Het |
Pip4k2a |
A |
G |
2: 18,852,433 (GRCm39) |
V283A |
probably benign |
Het |
Pkdrej |
A |
G |
15: 85,705,372 (GRCm39) |
V188A |
possibly damaging |
Het |
Pnpla6 |
T |
C |
8: 3,591,404 (GRCm39) |
W1151R |
probably damaging |
Het |
Ppp1r14c |
A |
G |
10: 3,316,890 (GRCm39) |
Y75C |
probably damaging |
Het |
Prl2b1 |
C |
T |
13: 27,567,452 (GRCm39) |
D224N |
probably benign |
Het |
Ptgis |
A |
G |
2: 167,056,778 (GRCm39) |
S270P |
probably benign |
Het |
Rgs11 |
C |
A |
17: 26,429,640 (GRCm39) |
A446D |
probably damaging |
Het |
Rims2 |
A |
G |
15: 39,545,098 (GRCm39) |
T1531A |
probably damaging |
Het |
Sbno1 |
A |
T |
5: 124,526,580 (GRCm39) |
|
probably benign |
Het |
Scarb2 |
C |
G |
5: 92,596,416 (GRCm39) |
M409I |
probably benign |
Het |
Scube3 |
C |
T |
17: 28,387,353 (GRCm39) |
|
probably benign |
Het |
Slc44a4 |
T |
C |
17: 35,140,901 (GRCm39) |
I180T |
probably damaging |
Het |
Slc9a2 |
T |
C |
1: 40,781,803 (GRCm39) |
M344T |
probably damaging |
Het |
Smc3 |
A |
T |
19: 53,627,800 (GRCm39) |
T860S |
probably benign |
Het |
Snrpa |
A |
G |
7: 26,891,174 (GRCm39) |
I99T |
probably benign |
Het |
Sorcs1 |
A |
G |
19: 50,163,481 (GRCm39) |
|
probably benign |
Het |
Sorl1 |
C |
T |
9: 41,902,778 (GRCm39) |
|
probably null |
Het |
Suds3 |
T |
C |
5: 117,243,309 (GRCm39) |
K143R |
probably benign |
Het |
Supt20 |
A |
T |
3: 54,622,164 (GRCm39) |
M424L |
probably benign |
Het |
Tgtp2 |
T |
C |
11: 48,949,751 (GRCm39) |
M274V |
probably benign |
Het |
Tmem158 |
T |
A |
9: 123,088,974 (GRCm39) |
M213L |
probably benign |
Het |
Tnks |
C |
A |
8: 35,324,672 (GRCm39) |
R639L |
probably benign |
Het |
Tns2 |
C |
T |
15: 102,017,369 (GRCm39) |
R281C |
probably damaging |
Het |
Trmt10c |
A |
C |
16: 55,854,938 (GRCm39) |
N232K |
possibly damaging |
Het |
Trpm6 |
C |
T |
19: 18,833,581 (GRCm39) |
R1587W |
probably damaging |
Het |
Trrap |
G |
A |
5: 144,765,400 (GRCm39) |
V2539I |
probably benign |
Het |
Tsg101 |
A |
G |
7: 46,556,835 (GRCm39) |
S115P |
probably benign |
Het |
Ttll13 |
G |
T |
7: 79,910,256 (GRCm39) |
V800L |
probably benign |
Het |
Vmn1r57 |
A |
G |
7: 5,223,576 (GRCm39) |
T34A |
possibly damaging |
Het |
Vmn2r118 |
T |
A |
17: 55,918,530 (GRCm39) |
T121S |
probably benign |
Het |
Wdr35 |
A |
G |
12: 9,035,772 (GRCm39) |
I238M |
possibly damaging |
Het |
Zfp81 |
T |
A |
17: 33,554,080 (GRCm39) |
T245S |
probably benign |
Het |
Zfyve26 |
G |
T |
12: 79,325,237 (GRCm39) |
P824Q |
probably damaging |
Het |
|
Other mutations in Pcnt |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01075:Pcnt
|
APN |
10 |
76,258,738 (GRCm39) |
nonsense |
probably null |
|
IGL01307:Pcnt
|
APN |
10 |
76,247,422 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01549:Pcnt
|
APN |
10 |
76,203,320 (GRCm39) |
splice site |
probably null |
|
IGL01576:Pcnt
|
APN |
10 |
76,204,656 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01611:Pcnt
|
APN |
10 |
76,272,258 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01630:Pcnt
|
APN |
10 |
76,256,080 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01647:Pcnt
|
APN |
10 |
76,205,835 (GRCm39) |
nonsense |
probably null |
|
IGL01689:Pcnt
|
APN |
10 |
76,247,487 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01690:Pcnt
|
APN |
10 |
76,228,609 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01723:Pcnt
|
APN |
10 |
76,254,333 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL01920:Pcnt
|
APN |
10 |
76,240,362 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01958:Pcnt
|
APN |
10 |
76,269,513 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02210:Pcnt
|
APN |
10 |
76,225,053 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02225:Pcnt
|
APN |
10 |
76,225,308 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02228:Pcnt
|
APN |
10 |
76,225,308 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02237:Pcnt
|
APN |
10 |
76,188,818 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02279:Pcnt
|
APN |
10 |
76,239,599 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02303:Pcnt
|
APN |
10 |
76,278,393 (GRCm39) |
splice site |
probably benign |
|
IGL02355:Pcnt
|
APN |
10 |
76,210,996 (GRCm39) |
nonsense |
probably null |
|
IGL02362:Pcnt
|
APN |
10 |
76,210,996 (GRCm39) |
nonsense |
probably null |
|
IGL02428:Pcnt
|
APN |
10 |
76,265,090 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02536:Pcnt
|
APN |
10 |
76,216,063 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL02715:Pcnt
|
APN |
10 |
76,204,556 (GRCm39) |
splice site |
probably benign |
|
IGL02800:Pcnt
|
APN |
10 |
76,248,417 (GRCm39) |
nonsense |
probably null |
|
IGL03395:Pcnt
|
APN |
10 |
76,272,325 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02799:Pcnt
|
UTSW |
10 |
76,248,417 (GRCm39) |
nonsense |
probably null |
|
PIT4520001:Pcnt
|
UTSW |
10 |
76,256,069 (GRCm39) |
missense |
probably damaging |
0.99 |
R0049:Pcnt
|
UTSW |
10 |
76,205,655 (GRCm39) |
unclassified |
probably benign |
|
R0049:Pcnt
|
UTSW |
10 |
76,205,655 (GRCm39) |
unclassified |
probably benign |
|
R0109:Pcnt
|
UTSW |
10 |
76,225,030 (GRCm39) |
missense |
probably benign |
0.00 |
R0117:Pcnt
|
UTSW |
10 |
76,244,561 (GRCm39) |
nonsense |
probably null |
|
R0254:Pcnt
|
UTSW |
10 |
76,228,414 (GRCm39) |
missense |
probably benign |
0.10 |
R0392:Pcnt
|
UTSW |
10 |
76,220,660 (GRCm39) |
missense |
probably benign |
|
R0511:Pcnt
|
UTSW |
10 |
76,240,429 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0570:Pcnt
|
UTSW |
10 |
76,247,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R0614:Pcnt
|
UTSW |
10 |
76,256,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R0635:Pcnt
|
UTSW |
10 |
76,240,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R0707:Pcnt
|
UTSW |
10 |
76,256,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R0749:Pcnt
|
UTSW |
10 |
76,217,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R0969:Pcnt
|
UTSW |
10 |
76,263,785 (GRCm39) |
missense |
probably damaging |
1.00 |
R1172:Pcnt
|
UTSW |
10 |
76,228,878 (GRCm39) |
splice site |
probably null |
|
R1174:Pcnt
|
UTSW |
10 |
76,228,878 (GRCm39) |
splice site |
probably null |
|
R1175:Pcnt
|
UTSW |
10 |
76,228,878 (GRCm39) |
splice site |
probably null |
|
R1512:Pcnt
|
UTSW |
10 |
76,240,496 (GRCm39) |
splice site |
probably null |
|
R1542:Pcnt
|
UTSW |
10 |
76,237,220 (GRCm39) |
missense |
probably benign |
0.02 |
R1542:Pcnt
|
UTSW |
10 |
76,225,221 (GRCm39) |
missense |
probably benign |
0.08 |
R1558:Pcnt
|
UTSW |
10 |
76,258,756 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1562:Pcnt
|
UTSW |
10 |
76,203,164 (GRCm39) |
missense |
probably benign |
0.02 |
R1762:Pcnt
|
UTSW |
10 |
76,190,971 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1869:Pcnt
|
UTSW |
10 |
76,215,740 (GRCm39) |
missense |
probably null |
0.94 |
R1911:Pcnt
|
UTSW |
10 |
76,204,650 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1985:Pcnt
|
UTSW |
10 |
76,216,171 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1995:Pcnt
|
UTSW |
10 |
76,228,633 (GRCm39) |
nonsense |
probably null |
|
R2073:Pcnt
|
UTSW |
10 |
76,216,214 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2111:Pcnt
|
UTSW |
10 |
76,256,360 (GRCm39) |
missense |
probably damaging |
0.99 |
R2112:Pcnt
|
UTSW |
10 |
76,256,360 (GRCm39) |
missense |
probably damaging |
0.99 |
R2309:Pcnt
|
UTSW |
10 |
76,278,460 (GRCm39) |
start gained |
probably benign |
|
R2902:Pcnt
|
UTSW |
10 |
76,211,064 (GRCm39) |
missense |
probably damaging |
0.98 |
R3623:Pcnt
|
UTSW |
10 |
76,269,584 (GRCm39) |
missense |
probably benign |
0.23 |
R4088:Pcnt
|
UTSW |
10 |
76,263,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R4300:Pcnt
|
UTSW |
10 |
76,203,225 (GRCm39) |
missense |
probably benign |
0.40 |
R4402:Pcnt
|
UTSW |
10 |
76,228,227 (GRCm39) |
missense |
probably benign |
0.00 |
R4407:Pcnt
|
UTSW |
10 |
76,210,704 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4483:Pcnt
|
UTSW |
10 |
76,237,317 (GRCm39) |
missense |
probably damaging |
1.00 |
R4647:Pcnt
|
UTSW |
10 |
76,190,047 (GRCm39) |
missense |
probably benign |
0.01 |
R4734:Pcnt
|
UTSW |
10 |
76,273,040 (GRCm39) |
missense |
probably benign |
0.25 |
R4747:Pcnt
|
UTSW |
10 |
76,272,299 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4782:Pcnt
|
UTSW |
10 |
76,245,411 (GRCm39) |
missense |
possibly damaging |
0.62 |
R4795:Pcnt
|
UTSW |
10 |
76,205,858 (GRCm39) |
missense |
probably benign |
0.21 |
R4831:Pcnt
|
UTSW |
10 |
76,248,335 (GRCm39) |
missense |
probably damaging |
0.96 |
R4873:Pcnt
|
UTSW |
10 |
76,205,688 (GRCm39) |
missense |
probably benign |
0.03 |
R4875:Pcnt
|
UTSW |
10 |
76,205,688 (GRCm39) |
missense |
probably benign |
0.03 |
R4946:Pcnt
|
UTSW |
10 |
76,192,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R5032:Pcnt
|
UTSW |
10 |
76,190,911 (GRCm39) |
missense |
probably benign |
0.00 |
R5033:Pcnt
|
UTSW |
10 |
76,235,779 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5106:Pcnt
|
UTSW |
10 |
76,237,278 (GRCm39) |
missense |
probably damaging |
1.00 |
R5118:Pcnt
|
UTSW |
10 |
76,248,002 (GRCm39) |
missense |
probably damaging |
0.98 |
R5167:Pcnt
|
UTSW |
10 |
76,256,258 (GRCm39) |
missense |
probably damaging |
0.97 |
R5199:Pcnt
|
UTSW |
10 |
76,254,378 (GRCm39) |
missense |
probably benign |
0.09 |
R5223:Pcnt
|
UTSW |
10 |
76,216,106 (GRCm39) |
missense |
probably damaging |
0.99 |
R5241:Pcnt
|
UTSW |
10 |
76,269,451 (GRCm39) |
missense |
probably benign |
0.26 |
R5308:Pcnt
|
UTSW |
10 |
76,192,159 (GRCm39) |
nonsense |
probably null |
|
R5328:Pcnt
|
UTSW |
10 |
76,247,553 (GRCm39) |
missense |
probably damaging |
1.00 |
R5454:Pcnt
|
UTSW |
10 |
76,225,381 (GRCm39) |
splice site |
probably null |
|
R5543:Pcnt
|
UTSW |
10 |
76,247,886 (GRCm39) |
missense |
probably benign |
0.01 |
R5588:Pcnt
|
UTSW |
10 |
76,278,445 (GRCm39) |
missense |
possibly damaging |
0.74 |
R5647:Pcnt
|
UTSW |
10 |
76,221,675 (GRCm39) |
missense |
probably benign |
0.17 |
R5668:Pcnt
|
UTSW |
10 |
76,245,334 (GRCm39) |
missense |
probably benign |
0.16 |
R5712:Pcnt
|
UTSW |
10 |
76,265,105 (GRCm39) |
missense |
probably damaging |
0.96 |
R5714:Pcnt
|
UTSW |
10 |
76,256,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R5797:Pcnt
|
UTSW |
10 |
76,228,590 (GRCm39) |
missense |
probably benign |
0.00 |
R5946:Pcnt
|
UTSW |
10 |
76,217,897 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5955:Pcnt
|
UTSW |
10 |
76,247,456 (GRCm39) |
missense |
possibly damaging |
0.45 |
R6024:Pcnt
|
UTSW |
10 |
76,255,871 (GRCm39) |
missense |
possibly damaging |
0.87 |
R6267:Pcnt
|
UTSW |
10 |
76,221,632 (GRCm39) |
missense |
probably benign |
0.02 |
R6485:Pcnt
|
UTSW |
10 |
76,225,164 (GRCm39) |
nonsense |
probably null |
|
R6605:Pcnt
|
UTSW |
10 |
76,265,032 (GRCm39) |
critical splice donor site |
probably null |
|
R6877:Pcnt
|
UTSW |
10 |
76,269,851 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6882:Pcnt
|
UTSW |
10 |
76,263,662 (GRCm39) |
missense |
probably benign |
0.00 |
R6919:Pcnt
|
UTSW |
10 |
76,221,632 (GRCm39) |
missense |
probably benign |
0.02 |
R7025:Pcnt
|
UTSW |
10 |
76,239,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R7098:Pcnt
|
UTSW |
10 |
76,220,673 (GRCm39) |
missense |
probably benign |
|
R7109:Pcnt
|
UTSW |
10 |
76,205,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R7121:Pcnt
|
UTSW |
10 |
76,263,761 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7143:Pcnt
|
UTSW |
10 |
76,224,894 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7152:Pcnt
|
UTSW |
10 |
76,247,194 (GRCm39) |
splice site |
probably null |
|
R7213:Pcnt
|
UTSW |
10 |
76,244,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R7368:Pcnt
|
UTSW |
10 |
76,235,835 (GRCm39) |
missense |
probably benign |
|
R7453:Pcnt
|
UTSW |
10 |
76,225,284 (GRCm39) |
missense |
probably benign |
|
R7486:Pcnt
|
UTSW |
10 |
76,254,271 (GRCm39) |
missense |
probably benign |
|
R7486:Pcnt
|
UTSW |
10 |
76,254,270 (GRCm39) |
missense |
probably benign |
0.03 |
R7538:Pcnt
|
UTSW |
10 |
76,235,773 (GRCm39) |
missense |
probably benign |
|
R7575:Pcnt
|
UTSW |
10 |
76,225,086 (GRCm39) |
missense |
probably benign |
0.32 |
R7662:Pcnt
|
UTSW |
10 |
76,223,356 (GRCm39) |
missense |
probably benign |
0.27 |
R7685:Pcnt
|
UTSW |
10 |
76,258,642 (GRCm39) |
missense |
probably benign |
0.14 |
R7764:Pcnt
|
UTSW |
10 |
76,190,082 (GRCm39) |
missense |
probably benign |
0.33 |
R7802:Pcnt
|
UTSW |
10 |
76,211,137 (GRCm39) |
splice site |
probably null |
|
R8432:Pcnt
|
UTSW |
10 |
76,256,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R8439:Pcnt
|
UTSW |
10 |
76,256,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R8493:Pcnt
|
UTSW |
10 |
76,239,457 (GRCm39) |
critical splice donor site |
probably null |
|
R8530:Pcnt
|
UTSW |
10 |
76,256,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R8535:Pcnt
|
UTSW |
10 |
76,256,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R8830:Pcnt
|
UTSW |
10 |
76,218,008 (GRCm39) |
missense |
probably benign |
0.03 |
R8878:Pcnt
|
UTSW |
10 |
76,244,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R8911:Pcnt
|
UTSW |
10 |
76,223,359 (GRCm39) |
missense |
probably damaging |
0.98 |
R8988:Pcnt
|
UTSW |
10 |
76,245,407 (GRCm39) |
nonsense |
probably null |
|
R9084:Pcnt
|
UTSW |
10 |
76,235,826 (GRCm39) |
missense |
probably benign |
0.09 |
R9169:Pcnt
|
UTSW |
10 |
76,221,572 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9372:Pcnt
|
UTSW |
10 |
76,258,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R9411:Pcnt
|
UTSW |
10 |
76,258,896 (GRCm39) |
missense |
probably damaging |
0.96 |
R9448:Pcnt
|
UTSW |
10 |
76,256,360 (GRCm39) |
missense |
probably damaging |
0.99 |
R9459:Pcnt
|
UTSW |
10 |
76,228,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R9479:Pcnt
|
UTSW |
10 |
76,217,963 (GRCm39) |
missense |
probably benign |
0.00 |
R9503:Pcnt
|
UTSW |
10 |
76,263,882 (GRCm39) |
missense |
possibly damaging |
0.59 |
R9561:Pcnt
|
UTSW |
10 |
76,217,128 (GRCm39) |
nonsense |
probably null |
|
R9618:Pcnt
|
UTSW |
10 |
76,188,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R9648:Pcnt
|
UTSW |
10 |
76,190,089 (GRCm39) |
missense |
probably benign |
0.32 |
R9733:Pcnt
|
UTSW |
10 |
76,237,314 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Pcnt
|
UTSW |
10 |
76,217,991 (GRCm39) |
nonsense |
probably null |
|
Z1177:Pcnt
|
UTSW |
10 |
76,235,802 (GRCm39) |
missense |
probably benign |
0.00 |
|