Other mutations in this stock |
Total: 105 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca4 |
T |
G |
3: 121,969,772 (GRCm39) |
L2259R |
probably damaging |
Het |
Acd |
A |
G |
8: 106,427,647 (GRCm39) |
S2P |
possibly damaging |
Het |
Acsf3 |
A |
G |
8: 123,506,896 (GRCm39) |
Y63C |
possibly damaging |
Het |
Adam21 |
T |
C |
12: 81,607,748 (GRCm39) |
I5V |
probably benign |
Het |
Adamts6 |
C |
A |
13: 104,580,636 (GRCm39) |
S783* |
probably null |
Het |
Adamtsl1 |
T |
C |
4: 86,162,006 (GRCm39) |
|
probably null |
Het |
Adck2 |
T |
A |
6: 39,553,327 (GRCm39) |
S313T |
probably benign |
Het |
Adgb |
A |
G |
10: 10,233,616 (GRCm39) |
I1285T |
probably benign |
Het |
Angptl1 |
T |
A |
1: 156,688,153 (GRCm39) |
M485K |
possibly damaging |
Het |
Ank3 |
G |
A |
10: 69,694,095 (GRCm39) |
V289I |
probably benign |
Het |
Atp13a4 |
A |
G |
16: 29,308,826 (GRCm39) |
|
probably null |
Het |
Atp1a1 |
A |
G |
3: 101,491,091 (GRCm39) |
L648P |
probably benign |
Het |
Atp2a3 |
A |
G |
11: 72,863,855 (GRCm39) |
I194V |
probably benign |
Het |
Bglap |
A |
C |
3: 88,291,712 (GRCm39) |
I4S |
unknown |
Het |
Cacna1b |
T |
A |
2: 24,527,499 (GRCm39) |
T1621S |
possibly damaging |
Het |
Ccdc112 |
T |
A |
18: 46,420,739 (GRCm39) |
Q337L |
probably benign |
Het |
Ccdc121rt3 |
A |
G |
5: 112,503,165 (GRCm39) |
S180P |
possibly damaging |
Het |
Cd34 |
T |
G |
1: 194,633,319 (GRCm39) |
S194A |
probably damaging |
Het |
Cdh20 |
A |
G |
1: 104,868,989 (GRCm39) |
D160G |
probably damaging |
Het |
Clock |
T |
C |
5: 76,413,763 (GRCm39) |
K44R |
probably damaging |
Het |
Commd9 |
A |
G |
2: 101,729,241 (GRCm39) |
N116D |
probably benign |
Het |
Dab2 |
C |
A |
15: 6,459,092 (GRCm39) |
P335T |
probably benign |
Het |
Epb41l3 |
T |
A |
17: 69,555,714 (GRCm39) |
|
probably null |
Het |
Epha2 |
A |
G |
4: 141,049,727 (GRCm39) |
|
probably null |
Het |
Fam78b |
T |
C |
1: 166,906,216 (GRCm39) |
V125A |
probably benign |
Het |
Fars2 |
A |
T |
13: 36,721,400 (GRCm39) |
E448V |
probably damaging |
Het |
Fkbpl |
G |
A |
17: 34,864,303 (GRCm39) |
A24T |
probably benign |
Het |
Glyr1 |
A |
C |
16: 4,865,622 (GRCm39) |
V44G |
probably benign |
Het |
Gm1527 |
A |
G |
3: 28,974,812 (GRCm39) |
I542V |
possibly damaging |
Het |
Gm18856 |
C |
A |
13: 14,139,793 (GRCm39) |
|
probably benign |
Het |
Gm44501 |
A |
G |
17: 40,889,605 (GRCm39) |
K40E |
probably benign |
Het |
Hdhd5 |
T |
C |
6: 120,500,407 (GRCm39) |
H97R |
probably benign |
Het |
Hmcn1 |
A |
G |
1: 150,629,362 (GRCm39) |
V965A |
probably benign |
Het |
Hsf5 |
A |
G |
11: 87,526,446 (GRCm39) |
M373V |
probably benign |
Het |
Igbp1b |
C |
T |
6: 138,634,803 (GRCm39) |
E214K |
probably benign |
Het |
Iigp1 |
T |
A |
18: 60,522,964 (GRCm39) |
F27L |
probably benign |
Het |
Isl1 |
T |
C |
13: 116,441,966 (GRCm39) |
N89S |
probably benign |
Het |
Itga1 |
C |
A |
13: 115,171,921 (GRCm39) |
W61C |
probably damaging |
Het |
Itga5 |
T |
C |
15: 103,256,187 (GRCm39) |
R922G |
probably benign |
Het |
Kbtbd3 |
G |
A |
9: 4,331,073 (GRCm39) |
W482* |
probably null |
Het |
Kcnq1 |
A |
G |
7: 142,736,494 (GRCm39) |
T168A |
probably benign |
Het |
Lrch3 |
A |
G |
16: 32,826,074 (GRCm39) |
N631S |
probably damaging |
Het |
Lrrk1 |
T |
A |
7: 65,912,413 (GRCm39) |
I1716F |
possibly damaging |
Het |
Ly75 |
T |
C |
2: 60,180,284 (GRCm39) |
E631G |
probably benign |
Het |
Map4 |
T |
C |
9: 109,864,331 (GRCm39) |
S519P |
probably benign |
Het |
Mroh2a |
A |
G |
1: 88,186,386 (GRCm39) |
S64G |
probably benign |
Het |
Mrtfa |
C |
T |
15: 80,901,234 (GRCm39) |
S419N |
probably damaging |
Het |
Muc5b |
A |
G |
7: 141,403,304 (GRCm39) |
E755G |
unknown |
Het |
Ncaph2 |
T |
G |
15: 89,255,010 (GRCm39) |
V478G |
probably damaging |
Het |
Ncbp1 |
A |
G |
4: 46,152,967 (GRCm39) |
R247G |
possibly damaging |
Het |
Necab1 |
G |
T |
4: 15,111,208 (GRCm39) |
D73E |
possibly damaging |
Het |
Nedd9 |
T |
C |
13: 41,471,376 (GRCm39) |
K208E |
probably benign |
Het |
Nfyb |
A |
T |
10: 82,588,202 (GRCm39) |
|
probably benign |
Het |
Nol4 |
T |
C |
18: 23,054,944 (GRCm39) |
Q162R |
probably damaging |
Het |
Nwd2 |
G |
A |
5: 63,962,776 (GRCm39) |
D787N |
probably benign |
Het |
Olfr908 |
T |
A |
9: 38,427,799 (GRCm39) |
M157K |
probably damaging |
Het |
Or10a5 |
A |
T |
7: 106,636,121 (GRCm39) |
Y253F |
probably benign |
Het |
Or11g7 |
A |
C |
14: 50,690,874 (GRCm39) |
M122L |
probably damaging |
Het |
Or13a22 |
A |
G |
7: 140,072,920 (GRCm39) |
D123G |
probably damaging |
Het |
Or5ac23 |
C |
T |
16: 59,149,213 (GRCm39) |
V220I |
probably benign |
Het |
Or6a2 |
C |
T |
7: 106,600,542 (GRCm39) |
G175D |
probably damaging |
Het |
Or6e1 |
A |
G |
14: 54,520,004 (GRCm39) |
M116T |
probably damaging |
Het |
Orai3 |
T |
C |
7: 127,373,060 (GRCm39) |
V187A |
probably benign |
Het |
Parn |
T |
C |
16: 13,424,066 (GRCm39) |
T444A |
probably benign |
Het |
Pcdh11x |
A |
C |
X: 119,309,937 (GRCm39) |
N460T |
probably damaging |
Het |
Pcnt |
C |
T |
10: 76,205,858 (GRCm39) |
R2516H |
probably benign |
Het |
Pde4d |
T |
A |
13: 110,074,705 (GRCm39) |
|
probably benign |
Het |
Pdgfra |
A |
G |
5: 75,349,972 (GRCm39) |
N952S |
probably benign |
Het |
Pgm2 |
A |
G |
5: 64,261,217 (GRCm39) |
Y237C |
probably damaging |
Het |
Plcb2 |
A |
G |
2: 118,541,605 (GRCm39) |
V975A |
probably benign |
Het |
Polk |
T |
C |
13: 96,625,764 (GRCm39) |
T347A |
probably benign |
Het |
Ppp6r1 |
C |
T |
7: 4,644,053 (GRCm39) |
V430M |
possibly damaging |
Het |
Ptges2 |
C |
A |
2: 32,286,334 (GRCm39) |
C16* |
probably null |
Het |
Relb |
A |
T |
7: 19,353,764 (GRCm39) |
I38N |
probably damaging |
Het |
Runx1t1 |
T |
A |
4: 13,837,767 (GRCm39) |
N51K |
probably damaging |
Het |
Samsn1 |
A |
G |
16: 75,680,733 (GRCm39) |
|
probably benign |
Het |
Scrn1 |
A |
G |
6: 54,497,754 (GRCm39) |
V279A |
possibly damaging |
Het |
Sec31b |
A |
G |
19: 44,520,185 (GRCm39) |
S200P |
probably benign |
Het |
Selp |
A |
G |
1: 163,972,475 (GRCm39) |
T705A |
probably benign |
Het |
Slc2a1 |
G |
A |
4: 118,989,642 (GRCm39) |
R61Q |
probably damaging |
Het |
Slit3 |
G |
A |
11: 35,542,647 (GRCm39) |
|
probably null |
Het |
Smo |
T |
A |
6: 29,755,573 (GRCm39) |
V415E |
probably damaging |
Het |
Spag8 |
C |
A |
4: 43,652,035 (GRCm39) |
V350L |
possibly damaging |
Het |
Tbck |
T |
G |
3: 132,413,559 (GRCm39) |
L132R |
possibly damaging |
Het |
Thnsl1 |
T |
A |
2: 21,216,856 (GRCm39) |
C203* |
probably null |
Het |
Tm9sf2 |
T |
A |
14: 122,387,252 (GRCm39) |
|
probably null |
Het |
Tmem131 |
A |
G |
1: 36,880,757 (GRCm39) |
V171A |
probably damaging |
Het |
Tmem209 |
T |
C |
6: 30,501,954 (GRCm39) |
T83A |
probably benign |
Het |
Tmem63a |
T |
C |
1: 180,782,416 (GRCm39) |
Y138H |
probably damaging |
Het |
Trim80 |
A |
G |
11: 115,338,769 (GRCm39) |
Y533C |
probably damaging |
Het |
Trpv2 |
A |
G |
11: 62,472,006 (GRCm39) |
D66G |
possibly damaging |
Het |
Trrap |
T |
A |
5: 144,769,298 (GRCm39) |
I2620N |
probably benign |
Het |
Ttyh3 |
A |
T |
5: 140,620,541 (GRCm39) |
I232N |
probably damaging |
Het |
Ube2dnl1 |
G |
A |
X: 113,815,482 (GRCm39) |
C119Y |
possibly damaging |
Het |
Unc13c |
T |
A |
9: 73,839,469 (GRCm39) |
S461C |
probably damaging |
Het |
Usp42 |
C |
A |
5: 143,709,692 (GRCm39) |
G170W |
probably damaging |
Het |
Vldlr |
T |
C |
19: 27,216,252 (GRCm39) |
|
probably null |
Het |
Ywhab |
A |
G |
2: 163,857,265 (GRCm39) |
Y180C |
probably damaging |
Het |
Zan |
A |
T |
5: 137,379,112 (GRCm39) |
C5329* |
probably null |
Het |
Zbtb40 |
C |
T |
4: 136,725,953 (GRCm39) |
M535I |
probably benign |
Het |
Zdhhc1 |
CGGGGG |
CGGGGGG |
8: 106,210,376 (GRCm39) |
|
probably null |
Het |
Zfp318 |
A |
G |
17: 46,722,988 (GRCm39) |
T1664A |
probably benign |
Het |
Zfp7 |
T |
A |
15: 76,775,546 (GRCm39) |
C529* |
probably null |
Het |
Zfp768 |
T |
C |
7: 126,942,547 (GRCm39) |
Q527R |
possibly damaging |
Het |
Zfp975 |
T |
A |
7: 42,314,570 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Unc80 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00160:Unc80
|
APN |
1 |
66,693,554 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL00340:Unc80
|
APN |
1 |
66,645,618 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL00783:Unc80
|
APN |
1 |
66,647,596 (GRCm39) |
missense |
probably benign |
0.37 |
IGL00784:Unc80
|
APN |
1 |
66,647,596 (GRCm39) |
missense |
probably benign |
0.37 |
IGL00935:Unc80
|
APN |
1 |
66,666,425 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL01094:Unc80
|
APN |
1 |
66,734,592 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01466:Unc80
|
APN |
1 |
66,661,645 (GRCm39) |
missense |
probably benign |
0.33 |
IGL01577:Unc80
|
APN |
1 |
66,569,127 (GRCm39) |
splice site |
probably null |
|
IGL01626:Unc80
|
APN |
1 |
66,590,213 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01640:Unc80
|
APN |
1 |
66,718,744 (GRCm39) |
missense |
probably benign |
0.33 |
IGL01775:Unc80
|
APN |
1 |
66,640,215 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01960:Unc80
|
APN |
1 |
66,647,659 (GRCm39) |
splice site |
probably benign |
|
IGL01991:Unc80
|
APN |
1 |
66,508,668 (GRCm39) |
nonsense |
probably null |
|
IGL02022:Unc80
|
APN |
1 |
66,665,675 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL02073:Unc80
|
APN |
1 |
66,651,386 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02077:Unc80
|
APN |
1 |
66,564,875 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL02197:Unc80
|
APN |
1 |
66,569,224 (GRCm39) |
missense |
probably benign |
0.39 |
IGL02198:Unc80
|
APN |
1 |
66,569,145 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02228:Unc80
|
APN |
1 |
66,647,587 (GRCm39) |
missense |
possibly damaging |
0.72 |
IGL02327:Unc80
|
APN |
1 |
66,680,832 (GRCm39) |
missense |
probably benign |
0.33 |
IGL02447:Unc80
|
APN |
1 |
66,542,703 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02489:Unc80
|
APN |
1 |
66,564,860 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02546:Unc80
|
APN |
1 |
66,594,112 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL02629:Unc80
|
APN |
1 |
66,522,476 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL02631:Unc80
|
APN |
1 |
66,569,222 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02839:Unc80
|
APN |
1 |
66,710,834 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL02960:Unc80
|
APN |
1 |
66,717,217 (GRCm39) |
splice site |
probably benign |
|
IGL02974:Unc80
|
APN |
1 |
66,564,817 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03060:Unc80
|
APN |
1 |
66,676,169 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL03062:Unc80
|
APN |
1 |
66,548,648 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03074:Unc80
|
APN |
1 |
66,710,877 (GRCm39) |
splice site |
probably benign |
|
IGL03086:Unc80
|
APN |
1 |
66,548,633 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03105:Unc80
|
APN |
1 |
66,511,258 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03107:Unc80
|
APN |
1 |
66,670,613 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03158:Unc80
|
APN |
1 |
66,680,833 (GRCm39) |
missense |
probably benign |
0.33 |
IGL03220:Unc80
|
APN |
1 |
66,544,097 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03271:Unc80
|
APN |
1 |
66,734,762 (GRCm39) |
unclassified |
probably benign |
|
IGL03332:Unc80
|
APN |
1 |
66,542,790 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03347:Unc80
|
APN |
1 |
66,734,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R0012:Unc80
|
UTSW |
1 |
66,546,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R0012:Unc80
|
UTSW |
1 |
66,546,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R0026:Unc80
|
UTSW |
1 |
66,560,743 (GRCm39) |
missense |
probably benign |
0.27 |
R0055:Unc80
|
UTSW |
1 |
66,545,782 (GRCm39) |
splice site |
probably benign |
|
R0149:Unc80
|
UTSW |
1 |
66,560,760 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0325:Unc80
|
UTSW |
1 |
66,550,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R0329:Unc80
|
UTSW |
1 |
66,713,246 (GRCm39) |
missense |
possibly damaging |
0.96 |
R0330:Unc80
|
UTSW |
1 |
66,713,246 (GRCm39) |
missense |
possibly damaging |
0.96 |
R0355:Unc80
|
UTSW |
1 |
66,589,015 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0412:Unc80
|
UTSW |
1 |
66,590,096 (GRCm39) |
splice site |
probably benign |
|
R0422:Unc80
|
UTSW |
1 |
66,522,497 (GRCm39) |
missense |
probably damaging |
1.00 |
R0477:Unc80
|
UTSW |
1 |
66,609,160 (GRCm39) |
missense |
probably damaging |
0.99 |
R0507:Unc80
|
UTSW |
1 |
66,567,052 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0513:Unc80
|
UTSW |
1 |
66,661,633 (GRCm39) |
missense |
possibly damaging |
0.73 |
R0553:Unc80
|
UTSW |
1 |
66,545,828 (GRCm39) |
missense |
probably damaging |
0.97 |
R0626:Unc80
|
UTSW |
1 |
66,647,601 (GRCm39) |
missense |
probably benign |
0.01 |
R0655:Unc80
|
UTSW |
1 |
66,542,940 (GRCm39) |
missense |
probably damaging |
0.98 |
R0742:Unc80
|
UTSW |
1 |
66,567,052 (GRCm39) |
missense |
possibly damaging |
0.66 |
R0755:Unc80
|
UTSW |
1 |
66,544,082 (GRCm39) |
missense |
probably damaging |
1.00 |
R0782:Unc80
|
UTSW |
1 |
66,661,740 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0837:Unc80
|
UTSW |
1 |
66,688,103 (GRCm39) |
missense |
possibly damaging |
0.73 |
R0841:Unc80
|
UTSW |
1 |
66,511,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R0893:Unc80
|
UTSW |
1 |
66,560,645 (GRCm39) |
missense |
probably damaging |
0.97 |
R0900:Unc80
|
UTSW |
1 |
66,710,757 (GRCm39) |
missense |
probably benign |
0.33 |
R0924:Unc80
|
UTSW |
1 |
66,549,800 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0930:Unc80
|
UTSW |
1 |
66,549,800 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0989:Unc80
|
UTSW |
1 |
66,685,599 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1145:Unc80
|
UTSW |
1 |
66,511,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R1145:Unc80
|
UTSW |
1 |
66,511,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R1224:Unc80
|
UTSW |
1 |
66,511,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R1240:Unc80
|
UTSW |
1 |
66,675,061 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1245:Unc80
|
UTSW |
1 |
66,594,254 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1467:Unc80
|
UTSW |
1 |
66,560,740 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1473:Unc80
|
UTSW |
1 |
66,560,740 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1500:Unc80
|
UTSW |
1 |
66,560,740 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1556:Unc80
|
UTSW |
1 |
66,560,740 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1562:Unc80
|
UTSW |
1 |
66,677,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R1655:Unc80
|
UTSW |
1 |
66,711,915 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1674:Unc80
|
UTSW |
1 |
66,548,467 (GRCm39) |
missense |
probably damaging |
1.00 |
R1680:Unc80
|
UTSW |
1 |
66,542,828 (GRCm39) |
nonsense |
probably null |
|
R1739:Unc80
|
UTSW |
1 |
66,567,051 (GRCm39) |
missense |
probably damaging |
0.97 |
R1756:Unc80
|
UTSW |
1 |
66,678,407 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1783:Unc80
|
UTSW |
1 |
66,722,432 (GRCm39) |
missense |
probably benign |
0.01 |
R1834:Unc80
|
UTSW |
1 |
66,678,407 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1854:Unc80
|
UTSW |
1 |
66,670,573 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1871:Unc80
|
UTSW |
1 |
66,549,876 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1878:Unc80
|
UTSW |
1 |
66,548,561 (GRCm39) |
missense |
probably damaging |
0.96 |
R1883:Unc80
|
UTSW |
1 |
66,564,929 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1912:Unc80
|
UTSW |
1 |
66,549,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R1990:Unc80
|
UTSW |
1 |
66,731,708 (GRCm39) |
missense |
probably damaging |
0.97 |
R2007:Unc80
|
UTSW |
1 |
66,542,935 (GRCm39) |
missense |
probably damaging |
1.00 |
R2035:Unc80
|
UTSW |
1 |
66,645,752 (GRCm39) |
missense |
probably damaging |
0.98 |
R2056:Unc80
|
UTSW |
1 |
66,679,711 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2060:Unc80
|
UTSW |
1 |
66,679,754 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2074:Unc80
|
UTSW |
1 |
66,718,903 (GRCm39) |
critical splice donor site |
probably null |
|
R2088:Unc80
|
UTSW |
1 |
66,629,386 (GRCm39) |
missense |
possibly damaging |
0.77 |
R2089:Unc80
|
UTSW |
1 |
66,710,874 (GRCm39) |
splice site |
probably benign |
|
R2091:Unc80
|
UTSW |
1 |
66,710,874 (GRCm39) |
splice site |
probably benign |
|
R2139:Unc80
|
UTSW |
1 |
66,560,740 (GRCm39) |
missense |
possibly damaging |
0.46 |
R2169:Unc80
|
UTSW |
1 |
66,560,740 (GRCm39) |
missense |
possibly damaging |
0.46 |
R2175:Unc80
|
UTSW |
1 |
66,716,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R2248:Unc80
|
UTSW |
1 |
66,662,365 (GRCm39) |
splice site |
probably benign |
|
R2255:Unc80
|
UTSW |
1 |
66,657,417 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2308:Unc80
|
UTSW |
1 |
66,688,156 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2484:Unc80
|
UTSW |
1 |
66,560,740 (GRCm39) |
missense |
possibly damaging |
0.46 |
R2507:Unc80
|
UTSW |
1 |
66,651,266 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2512:Unc80
|
UTSW |
1 |
66,710,767 (GRCm39) |
missense |
possibly damaging |
0.70 |
R2878:Unc80
|
UTSW |
1 |
66,710,735 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R3040:Unc80
|
UTSW |
1 |
66,678,464 (GRCm39) |
missense |
probably benign |
0.33 |
R3104:Unc80
|
UTSW |
1 |
66,662,450 (GRCm39) |
missense |
probably benign |
0.33 |
R3402:Unc80
|
UTSW |
1 |
66,549,845 (GRCm39) |
missense |
probably damaging |
0.97 |
R3403:Unc80
|
UTSW |
1 |
66,549,845 (GRCm39) |
missense |
probably damaging |
0.97 |
R3413:Unc80
|
UTSW |
1 |
66,678,464 (GRCm39) |
missense |
probably benign |
0.33 |
R3426:Unc80
|
UTSW |
1 |
66,678,464 (GRCm39) |
missense |
probably benign |
0.33 |
R3427:Unc80
|
UTSW |
1 |
66,678,464 (GRCm39) |
missense |
probably benign |
0.33 |
R3428:Unc80
|
UTSW |
1 |
66,678,464 (GRCm39) |
missense |
probably benign |
0.33 |
R3904:Unc80
|
UTSW |
1 |
66,678,455 (GRCm39) |
nonsense |
probably null |
|
R3916:Unc80
|
UTSW |
1 |
66,716,654 (GRCm39) |
missense |
probably benign |
0.11 |
R3950:Unc80
|
UTSW |
1 |
66,661,729 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4642:Unc80
|
UTSW |
1 |
66,710,873 (GRCm39) |
splice site |
probably null |
|
R4646:Unc80
|
UTSW |
1 |
66,708,394 (GRCm39) |
missense |
probably benign |
0.03 |
R4655:Unc80
|
UTSW |
1 |
66,710,821 (GRCm39) |
missense |
probably benign |
0.18 |
R4662:Unc80
|
UTSW |
1 |
66,685,595 (GRCm39) |
missense |
probably benign |
0.01 |
R4720:Unc80
|
UTSW |
1 |
66,549,951 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4736:Unc80
|
UTSW |
1 |
66,688,831 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4888:Unc80
|
UTSW |
1 |
66,683,606 (GRCm39) |
missense |
probably damaging |
0.98 |
R4917:Unc80
|
UTSW |
1 |
66,685,709 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4918:Unc80
|
UTSW |
1 |
66,685,709 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4983:Unc80
|
UTSW |
1 |
66,713,891 (GRCm39) |
splice site |
probably null |
|
R5051:Unc80
|
UTSW |
1 |
66,548,636 (GRCm39) |
missense |
probably damaging |
0.96 |
R5111:Unc80
|
UTSW |
1 |
66,567,154 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5122:Unc80
|
UTSW |
1 |
66,718,749 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5260:Unc80
|
UTSW |
1 |
66,685,746 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5351:Unc80
|
UTSW |
1 |
66,645,672 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5387:Unc80
|
UTSW |
1 |
66,569,180 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5437:Unc80
|
UTSW |
1 |
66,693,737 (GRCm39) |
missense |
possibly damaging |
0.96 |
R5525:Unc80
|
UTSW |
1 |
66,645,773 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5621:Unc80
|
UTSW |
1 |
66,677,202 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5690:Unc80
|
UTSW |
1 |
66,679,731 (GRCm39) |
missense |
probably benign |
0.08 |
R5762:Unc80
|
UTSW |
1 |
66,732,955 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5956:Unc80
|
UTSW |
1 |
66,567,123 (GRCm39) |
missense |
probably damaging |
0.97 |
R6005:Unc80
|
UTSW |
1 |
66,666,416 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6025:Unc80
|
UTSW |
1 |
66,734,727 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6033:Unc80
|
UTSW |
1 |
66,512,419 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6033:Unc80
|
UTSW |
1 |
66,512,419 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6117:Unc80
|
UTSW |
1 |
66,714,226 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6156:Unc80
|
UTSW |
1 |
66,651,409 (GRCm39) |
missense |
probably benign |
0.01 |
R6157:Unc80
|
UTSW |
1 |
66,693,188 (GRCm39) |
nonsense |
probably null |
|
R6189:Unc80
|
UTSW |
1 |
66,716,630 (GRCm39) |
missense |
probably benign |
0.33 |
R6291:Unc80
|
UTSW |
1 |
66,560,756 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6367:Unc80
|
UTSW |
1 |
66,711,925 (GRCm39) |
missense |
probably benign |
0.33 |
R6598:Unc80
|
UTSW |
1 |
66,507,699 (GRCm39) |
critical splice donor site |
probably null |
|
R6724:Unc80
|
UTSW |
1 |
66,722,350 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6763:Unc80
|
UTSW |
1 |
66,560,636 (GRCm39) |
missense |
probably benign |
0.00 |
R6773:Unc80
|
UTSW |
1 |
66,690,702 (GRCm39) |
missense |
probably benign |
0.33 |
R6883:Unc80
|
UTSW |
1 |
66,685,563 (GRCm39) |
missense |
probably benign |
0.33 |
R6951:Unc80
|
UTSW |
1 |
66,687,670 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6965:Unc80
|
UTSW |
1 |
66,685,725 (GRCm39) |
missense |
probably benign |
0.33 |
R6993:Unc80
|
UTSW |
1 |
66,588,952 (GRCm39) |
missense |
possibly damaging |
0.60 |
R7041:Unc80
|
UTSW |
1 |
66,542,752 (GRCm39) |
missense |
probably benign |
0.00 |
R7050:Unc80
|
UTSW |
1 |
66,590,067 (GRCm39) |
splice site |
probably null |
|
R7067:Unc80
|
UTSW |
1 |
66,685,731 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7080:Unc80
|
UTSW |
1 |
66,685,680 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7193:Unc80
|
UTSW |
1 |
66,588,943 (GRCm39) |
missense |
possibly damaging |
0.60 |
R7197:Unc80
|
UTSW |
1 |
66,560,725 (GRCm39) |
nonsense |
probably null |
|
R7278:Unc80
|
UTSW |
1 |
66,591,368 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7290:Unc80
|
UTSW |
1 |
66,640,356 (GRCm39) |
missense |
probably damaging |
0.97 |
R7391:Unc80
|
UTSW |
1 |
66,734,687 (GRCm39) |
missense |
probably benign |
0.18 |
R7401:Unc80
|
UTSW |
1 |
66,685,574 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7470:Unc80
|
UTSW |
1 |
66,661,621 (GRCm39) |
missense |
probably benign |
0.02 |
R7573:Unc80
|
UTSW |
1 |
66,560,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R7637:Unc80
|
UTSW |
1 |
66,711,843 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7678:Unc80
|
UTSW |
1 |
66,688,881 (GRCm39) |
missense |
probably benign |
0.33 |
R7697:Unc80
|
UTSW |
1 |
66,677,104 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7746:Unc80
|
UTSW |
1 |
66,716,544 (GRCm39) |
missense |
probably benign |
0.33 |
R7768:Unc80
|
UTSW |
1 |
66,549,754 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7796:Unc80
|
UTSW |
1 |
66,542,873 (GRCm39) |
missense |
probably benign |
|
R7855:Unc80
|
UTSW |
1 |
66,522,508 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7878:Unc80
|
UTSW |
1 |
66,640,300 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7879:Unc80
|
UTSW |
1 |
66,549,866 (GRCm39) |
missense |
probably benign |
0.00 |
R8024:Unc80
|
UTSW |
1 |
66,645,803 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8026:Unc80
|
UTSW |
1 |
66,522,463 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8115:Unc80
|
UTSW |
1 |
66,688,072 (GRCm39) |
missense |
probably benign |
0.00 |
R8135:Unc80
|
UTSW |
1 |
66,548,446 (GRCm39) |
missense |
possibly damaging |
0.49 |
R8170:Unc80
|
UTSW |
1 |
66,690,692 (GRCm39) |
missense |
probably benign |
0.33 |
R8239:Unc80
|
UTSW |
1 |
66,693,178 (GRCm39) |
missense |
probably benign |
|
R8249:Unc80
|
UTSW |
1 |
66,658,650 (GRCm39) |
missense |
probably benign |
0.01 |
R8275:Unc80
|
UTSW |
1 |
66,679,773 (GRCm39) |
nonsense |
probably null |
|
R8288:Unc80
|
UTSW |
1 |
66,512,509 (GRCm39) |
missense |
probably benign |
0.07 |
R8341:Unc80
|
UTSW |
1 |
66,688,192 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8356:Unc80
|
UTSW |
1 |
66,680,788 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8433:Unc80
|
UTSW |
1 |
66,677,187 (GRCm39) |
nonsense |
probably null |
|
R8456:Unc80
|
UTSW |
1 |
66,680,788 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8464:Unc80
|
UTSW |
1 |
66,512,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R8483:Unc80
|
UTSW |
1 |
66,732,869 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8509:Unc80
|
UTSW |
1 |
66,680,788 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8686:Unc80
|
UTSW |
1 |
66,651,427 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8701:Unc80
|
UTSW |
1 |
66,677,191 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8729:Unc80
|
UTSW |
1 |
66,647,649 (GRCm39) |
missense |
probably benign |
0.01 |
R8755:Unc80
|
UTSW |
1 |
66,651,290 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8771:Unc80
|
UTSW |
1 |
66,685,554 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8866:Unc80
|
UTSW |
1 |
66,629,388 (GRCm39) |
missense |
probably benign |
0.05 |
R8877:Unc80
|
UTSW |
1 |
66,567,144 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8942:Unc80
|
UTSW |
1 |
66,512,468 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8976:Unc80
|
UTSW |
1 |
66,511,169 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9063:Unc80
|
UTSW |
1 |
66,645,816 (GRCm39) |
critical splice donor site |
probably null |
|
R9095:Unc80
|
UTSW |
1 |
66,545,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R9125:Unc80
|
UTSW |
1 |
66,718,740 (GRCm39) |
missense |
probably benign |
0.18 |
R9130:Unc80
|
UTSW |
1 |
66,677,244 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9165:Unc80
|
UTSW |
1 |
66,589,000 (GRCm39) |
missense |
probably null |
0.95 |
R9220:Unc80
|
UTSW |
1 |
66,546,534 (GRCm39) |
missense |
probably damaging |
1.00 |
R9262:Unc80
|
UTSW |
1 |
66,594,411 (GRCm39) |
intron |
probably benign |
|
R9334:Unc80
|
UTSW |
1 |
66,688,919 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9374:Unc80
|
UTSW |
1 |
66,629,460 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9387:Unc80
|
UTSW |
1 |
66,589,097 (GRCm39) |
critical splice donor site |
probably null |
|
R9415:Unc80
|
UTSW |
1 |
66,550,064 (GRCm39) |
missense |
|
|
R9427:Unc80
|
UTSW |
1 |
66,594,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R9436:Unc80
|
UTSW |
1 |
66,732,964 (GRCm39) |
critical splice donor site |
probably null |
|
R9454:Unc80
|
UTSW |
1 |
66,734,749 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9522:Unc80
|
UTSW |
1 |
66,677,221 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9539:Unc80
|
UTSW |
1 |
66,609,163 (GRCm39) |
critical splice donor site |
probably null |
|
R9552:Unc80
|
UTSW |
1 |
66,717,282 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9667:Unc80
|
UTSW |
1 |
66,651,287 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9720:Unc80
|
UTSW |
1 |
66,683,485 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9749:Unc80
|
UTSW |
1 |
66,544,179 (GRCm39) |
missense |
probably damaging |
0.99 |
R9789:Unc80
|
UTSW |
1 |
66,651,371 (GRCm39) |
missense |
possibly damaging |
0.53 |
X0019:Unc80
|
UTSW |
1 |
66,687,541 (GRCm39) |
missense |
probably benign |
0.33 |
X0021:Unc80
|
UTSW |
1 |
66,548,425 (GRCm39) |
critical splice acceptor site |
probably null |
|
X0024:Unc80
|
UTSW |
1 |
66,530,205 (GRCm39) |
missense |
probably benign |
0.21 |
X0062:Unc80
|
UTSW |
1 |
66,662,418 (GRCm39) |
missense |
probably benign |
0.02 |
X0066:Unc80
|
UTSW |
1 |
66,569,916 (GRCm39) |
missense |
possibly damaging |
0.77 |
Y4335:Unc80
|
UTSW |
1 |
66,560,740 (GRCm39) |
missense |
possibly damaging |
0.46 |
Y4336:Unc80
|
UTSW |
1 |
66,560,740 (GRCm39) |
missense |
possibly damaging |
0.46 |
Y4338:Unc80
|
UTSW |
1 |
66,560,740 (GRCm39) |
missense |
possibly damaging |
0.46 |
Z1088:Unc80
|
UTSW |
1 |
66,685,610 (GRCm39) |
missense |
possibly damaging |
0.85 |
Z1176:Unc80
|
UTSW |
1 |
66,733,568 (GRCm39) |
missense |
probably benign |
|
Z1177:Unc80
|
UTSW |
1 |
66,734,498 (GRCm39) |
missense |
probably benign |
0.03 |
Z1177:Unc80
|
UTSW |
1 |
66,685,557 (GRCm39) |
missense |
possibly damaging |
0.72 |
|