Other mutations in this stock |
Total: 107 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
T |
11: 9,349,430 (GRCm39) |
H3668L |
probably damaging |
Het |
Acsbg3 |
A |
T |
17: 57,190,631 (GRCm39) |
I400F |
probably benign |
Het |
Acvr1c |
T |
C |
2: 58,174,850 (GRCm39) |
T313A |
probably damaging |
Het |
Adam28 |
T |
C |
14: 68,855,188 (GRCm39) |
K651R |
probably damaging |
Het |
Adamtsl3 |
A |
T |
7: 82,171,198 (GRCm39) |
D417V |
probably damaging |
Het |
Adgrf4 |
A |
T |
17: 42,978,204 (GRCm39) |
C380S |
probably damaging |
Het |
AI597479 |
T |
G |
1: 43,150,277 (GRCm39) |
L129R |
probably benign |
Het |
Anpep |
C |
T |
7: 79,488,004 (GRCm39) |
E518K |
probably benign |
Het |
Anxa7 |
A |
C |
14: 20,519,566 (GRCm39) |
|
probably null |
Het |
Arb2a |
T |
A |
13: 77,910,070 (GRCm39) |
|
probably benign |
Het |
Arhgap22 |
A |
G |
14: 33,091,374 (GRCm39) |
R650G |
possibly damaging |
Het |
Atp8a1 |
T |
A |
5: 67,969,416 (GRCm39) |
|
probably benign |
Het |
Bcr |
C |
T |
10: 75,017,466 (GRCm39) |
T1209I |
possibly damaging |
Het |
Bmpr1a |
C |
T |
14: 34,151,734 (GRCm39) |
S185N |
probably benign |
Het |
Calcoco1 |
A |
T |
15: 102,624,198 (GRCm39) |
M246K |
probably benign |
Het |
Casp12 |
T |
A |
9: 5,345,534 (GRCm39) |
|
probably benign |
Het |
Ccno |
T |
A |
13: 113,126,530 (GRCm39) |
L333Q |
probably damaging |
Het |
Cdhr2 |
T |
A |
13: 54,882,614 (GRCm39) |
|
probably benign |
Het |
Cftr |
T |
A |
6: 18,226,096 (GRCm39) |
M318K |
probably null |
Het |
Ckmt2 |
T |
A |
13: 92,011,322 (GRCm39) |
D96V |
possibly damaging |
Het |
Cnnm1 |
C |
T |
19: 43,430,349 (GRCm39) |
P489L |
probably damaging |
Het |
Cntnap1 |
A |
T |
11: 101,079,135 (GRCm39) |
D1175V |
probably damaging |
Het |
Cpne5 |
A |
T |
17: 29,430,634 (GRCm39) |
L92H |
probably damaging |
Het |
Crcp |
C |
A |
5: 130,071,083 (GRCm39) |
Q61K |
possibly damaging |
Het |
Crppa |
C |
T |
12: 36,431,837 (GRCm39) |
A22V |
possibly damaging |
Het |
Dcaf8 |
T |
A |
1: 172,014,978 (GRCm39) |
D414E |
probably benign |
Het |
Ddx28 |
T |
C |
8: 106,736,877 (GRCm39) |
T394A |
probably benign |
Het |
Ddx55 |
T |
C |
5: 124,697,210 (GRCm39) |
F191L |
probably benign |
Het |
Dnaaf1 |
T |
C |
8: 120,322,756 (GRCm39) |
|
probably benign |
Het |
Dnaaf2 |
C |
A |
12: 69,244,518 (GRCm39) |
R181L |
probably damaging |
Het |
Elac2 |
A |
G |
11: 64,870,136 (GRCm39) |
Y67C |
probably damaging |
Het |
Elf5 |
A |
G |
2: 103,260,765 (GRCm39) |
|
probably benign |
Het |
Emcn |
T |
A |
3: 137,122,575 (GRCm39) |
|
probably benign |
Het |
Erbb4 |
T |
C |
1: 68,337,439 (GRCm39) |
|
probably benign |
Het |
Erbin |
C |
A |
13: 104,005,373 (GRCm39) |
C114F |
probably damaging |
Het |
Etfdh |
T |
C |
3: 79,517,151 (GRCm39) |
I353V |
probably benign |
Het |
Fads2b |
T |
A |
2: 85,348,895 (GRCm39) |
R72S |
probably benign |
Het |
Fbxl12 |
C |
T |
9: 20,549,776 (GRCm39) |
G316D |
probably damaging |
Het |
Gbf1 |
G |
A |
19: 46,260,709 (GRCm39) |
|
probably null |
Het |
Gbp2b |
T |
G |
3: 142,313,937 (GRCm39) |
S406A |
probably benign |
Het |
Gli3 |
T |
G |
13: 15,898,143 (GRCm39) |
L741R |
probably damaging |
Het |
Gmip |
G |
T |
8: 70,263,468 (GRCm39) |
S70I |
probably benign |
Het |
Gnptab |
T |
C |
10: 88,276,171 (GRCm39) |
S1153P |
probably damaging |
Het |
Gp1ba |
A |
G |
11: 70,531,235 (GRCm39) |
|
probably benign |
Het |
Gramd1a |
T |
C |
7: 30,837,679 (GRCm39) |
D360G |
possibly damaging |
Het |
Hectd4 |
T |
C |
5: 121,397,927 (GRCm39) |
I285T |
probably benign |
Het |
Hrh4 |
A |
G |
18: 13,140,302 (GRCm39) |
|
probably benign |
Het |
Hsp90b1 |
T |
C |
10: 86,530,019 (GRCm39) |
E226G |
probably damaging |
Het |
Hspa13 |
A |
T |
16: 75,562,018 (GRCm39) |
D60E |
probably damaging |
Het |
Htt |
T |
A |
5: 34,974,478 (GRCm39) |
|
probably benign |
Het |
Iqca1l |
T |
C |
5: 24,750,783 (GRCm39) |
|
probably null |
Het |
Kif14 |
G |
C |
1: 136,423,764 (GRCm39) |
|
probably benign |
Het |
Kit |
T |
G |
5: 75,813,489 (GRCm39) |
V888G |
probably damaging |
Het |
Lpin3 |
T |
C |
2: 160,747,225 (GRCm39) |
V827A |
probably benign |
Het |
Lrriq4 |
T |
C |
3: 30,709,873 (GRCm39) |
S406P |
probably benign |
Het |
Man2c1 |
T |
C |
9: 57,048,467 (GRCm39) |
V777A |
probably benign |
Het |
Mcm8 |
A |
G |
2: 132,661,914 (GRCm39) |
K83E |
possibly damaging |
Het |
Mep1a |
A |
G |
17: 43,808,789 (GRCm39) |
|
probably null |
Het |
Mtor |
T |
A |
4: 148,568,837 (GRCm39) |
V1119E |
probably benign |
Het |
Mybpc2 |
C |
T |
7: 44,158,453 (GRCm39) |
A710T |
possibly damaging |
Het |
Myo9a |
C |
G |
9: 59,830,960 (GRCm39) |
T2368S |
probably damaging |
Het |
Nbeal1 |
A |
G |
1: 60,307,222 (GRCm39) |
Y1684C |
probably damaging |
Het |
Npm3 |
A |
G |
19: 45,737,965 (GRCm39) |
F11L |
probably benign |
Het |
Nutf2 |
T |
A |
8: 106,602,995 (GRCm39) |
S37T |
probably damaging |
Het |
Obscn |
T |
A |
11: 58,931,267 (GRCm39) |
I5790F |
probably damaging |
Het |
Obscn |
A |
T |
11: 58,943,332 (GRCm39) |
D4833E |
probably damaging |
Het |
Or2g1 |
A |
T |
17: 38,106,880 (GRCm39) |
M182L |
probably benign |
Het |
Or7d9 |
T |
A |
9: 20,197,153 (GRCm39) |
S61T |
possibly damaging |
Het |
Or8g35 |
T |
C |
9: 39,381,852 (GRCm39) |
T57A |
possibly damaging |
Het |
Or9g4b |
T |
A |
2: 85,616,147 (GRCm39) |
C97* |
probably null |
Het |
Pcdhb1 |
A |
G |
18: 37,400,077 (GRCm39) |
D676G |
possibly damaging |
Het |
Pcif1 |
G |
T |
2: 164,731,364 (GRCm39) |
R466L |
probably damaging |
Het |
Pdk1 |
T |
C |
2: 71,726,018 (GRCm39) |
|
probably benign |
Het |
Phxr2 |
T |
C |
10: 98,961,979 (GRCm39) |
|
probably benign |
Het |
Pidd1 |
A |
T |
7: 141,019,474 (GRCm39) |
|
probably benign |
Het |
Plec |
A |
G |
15: 76,075,618 (GRCm39) |
|
probably null |
Het |
Polr1a |
T |
A |
6: 71,943,400 (GRCm39) |
C1212S |
possibly damaging |
Het |
Pot1a |
A |
G |
6: 25,778,830 (GRCm39) |
|
probably benign |
Het |
Prdm5 |
T |
C |
6: 65,839,887 (GRCm39) |
|
probably benign |
Het |
Primpol |
A |
T |
8: 47,063,496 (GRCm39) |
N53K |
probably damaging |
Het |
Pyroxd1 |
A |
G |
6: 142,307,702 (GRCm39) |
I491V |
probably benign |
Het |
Serpinb3b |
G |
T |
1: 107,087,433 (GRCm39) |
N25K |
probably damaging |
Het |
Slc9b1 |
C |
T |
3: 135,078,996 (GRCm39) |
R218* |
probably null |
Het |
Ssbp2 |
T |
A |
13: 91,828,698 (GRCm39) |
|
probably null |
Het |
Stat4 |
A |
G |
1: 52,130,029 (GRCm39) |
|
probably benign |
Het |
Steap4 |
T |
C |
5: 8,025,829 (GRCm39) |
V130A |
possibly damaging |
Het |
Stoml2 |
A |
G |
4: 43,030,238 (GRCm39) |
|
probably null |
Het |
Syne2 |
G |
T |
12: 76,013,727 (GRCm39) |
G2974C |
probably benign |
Het |
Tfdp2 |
T |
G |
9: 96,188,946 (GRCm39) |
F200V |
probably damaging |
Het |
Tgm4 |
T |
C |
9: 122,877,622 (GRCm39) |
|
probably null |
Het |
Tie1 |
C |
A |
4: 118,341,924 (GRCm39) |
R175L |
probably benign |
Het |
Tmem145 |
A |
G |
7: 25,008,099 (GRCm39) |
|
probably benign |
Het |
Tsacc |
A |
G |
3: 88,190,169 (GRCm39) |
S94P |
possibly damaging |
Het |
Tshz3 |
T |
A |
7: 36,469,458 (GRCm39) |
D482E |
probably benign |
Het |
Tspan33 |
T |
C |
6: 29,711,091 (GRCm39) |
|
probably null |
Het |
Ugt2b35 |
A |
G |
5: 87,151,264 (GRCm39) |
K290R |
probably null |
Het |
Usp10 |
T |
A |
8: 120,663,296 (GRCm39) |
C39* |
probably null |
Het |
Utp20 |
T |
A |
10: 88,653,841 (GRCm39) |
T260S |
probably benign |
Het |
Vmn2r118 |
G |
T |
17: 55,917,717 (GRCm39) |
T265K |
probably damaging |
Het |
Vmn2r7 |
C |
A |
3: 64,598,439 (GRCm39) |
C797F |
probably damaging |
Het |
Vmn2r98 |
A |
C |
17: 19,286,609 (GRCm39) |
H369P |
probably benign |
Het |
Vps39 |
A |
T |
2: 120,169,268 (GRCm39) |
Y245N |
possibly damaging |
Het |
Wdr27 |
A |
G |
17: 15,154,721 (GRCm39) |
|
probably benign |
Het |
Ythdc2 |
A |
G |
18: 44,998,127 (GRCm39) |
|
probably benign |
Het |
Zcwpw2 |
C |
A |
9: 117,843,123 (GRCm39) |
|
noncoding transcript |
Het |
Zdhhc1 |
C |
A |
8: 106,210,175 (GRCm39) |
A81S |
probably benign |
Het |
Zfp729a |
G |
T |
13: 67,768,473 (GRCm39) |
H585Q |
probably damaging |
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 |
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 |
|
R4795:Unc80
|
UTSW |
1 |
66,567,100 (GRCm39) |
missense |
probably damaging |
0.97 |
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 |
|