Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2210408I21Rik |
T |
C |
13: 77,340,766 (GRCm39) |
S132P |
probably benign |
Het |
AC153895.1 |
T |
C |
6: 50,020,451 (GRCm39) |
R54G |
unknown |
Het |
Acot12 |
G |
A |
13: 91,919,994 (GRCm39) |
|
probably null |
Het |
Adhfe1 |
T |
A |
1: 9,623,671 (GRCm39) |
D98E |
probably benign |
Het |
Ago2 |
A |
G |
15: 72,988,213 (GRCm39) |
F594S |
probably damaging |
Het |
Aldh18a1 |
A |
G |
19: 40,545,927 (GRCm39) |
I620T |
probably damaging |
Het |
Aspscr1 |
C |
A |
11: 120,592,342 (GRCm39) |
A294D |
probably damaging |
Het |
Bod1l |
C |
G |
5: 41,976,883 (GRCm39) |
R1477T |
probably damaging |
Het |
Ccdc18 |
C |
A |
5: 108,336,844 (GRCm39) |
A741D |
possibly damaging |
Het |
Ces4a |
G |
A |
8: 105,864,729 (GRCm39) |
G69S |
probably damaging |
Het |
Cfap52 |
C |
T |
11: 67,829,819 (GRCm39) |
V317I |
probably benign |
Het |
Cgn |
A |
T |
3: 94,681,568 (GRCm39) |
L509Q |
probably benign |
Het |
Crb2 |
A |
G |
2: 37,676,631 (GRCm39) |
H204R |
probably benign |
Het |
Cspg4b |
A |
G |
13: 113,504,790 (GRCm39) |
N431S |
probably damaging |
Het |
Ddx39a |
G |
A |
8: 84,446,527 (GRCm39) |
V99M |
probably damaging |
Het |
Dis3l2 |
T |
A |
1: 86,948,808 (GRCm39) |
C582S |
possibly damaging |
Het |
Dmbt1 |
G |
A |
7: 130,676,061 (GRCm39) |
|
probably benign |
Het |
Dnah6 |
T |
C |
6: 73,004,425 (GRCm39) |
E3846G |
probably damaging |
Het |
Dstyk |
A |
G |
1: 132,384,084 (GRCm39) |
E655G |
probably damaging |
Het |
Epha4 |
T |
C |
1: 77,357,523 (GRCm39) |
Y825C |
probably damaging |
Het |
Esp36 |
T |
A |
17: 38,728,173 (GRCm39) |
N36I |
probably damaging |
Het |
Fabp3 |
C |
T |
4: 130,206,180 (GRCm39) |
T57I |
probably benign |
Het |
Fem1c |
A |
G |
18: 46,657,280 (GRCm39) |
S145P |
probably benign |
Het |
Galnt13 |
T |
C |
2: 54,623,094 (GRCm39) |
I80T |
probably damaging |
Het |
Gm5698 |
T |
C |
1: 31,016,728 (GRCm39) |
T108A |
probably benign |
Het |
Hipk3 |
A |
G |
2: 104,271,607 (GRCm39) |
S442P |
probably benign |
Het |
Hmcn2 |
T |
A |
2: 31,204,491 (GRCm39) |
V22D |
possibly damaging |
Het |
Hspg2 |
C |
T |
4: 137,238,552 (GRCm39) |
|
probably benign |
Het |
Ide |
A |
G |
19: 37,262,603 (GRCm39) |
|
probably null |
Het |
Ifnar1 |
C |
A |
16: 91,300,384 (GRCm39) |
P462Q |
probably damaging |
Het |
Itgb2l |
T |
A |
16: 96,228,049 (GRCm39) |
I485F |
probably benign |
Het |
Jakmip3 |
C |
T |
7: 138,629,505 (GRCm39) |
R549W |
possibly damaging |
Het |
Lrrc36 |
A |
G |
8: 106,187,761 (GRCm39) |
Q680R |
probably damaging |
Het |
Lysmd3 |
T |
G |
13: 81,817,390 (GRCm39) |
H122Q |
probably benign |
Het |
Macf1 |
C |
A |
4: 123,577,802 (GRCm39) |
V61L |
possibly damaging |
Het |
Map1b |
T |
C |
13: 99,568,036 (GRCm39) |
T1562A |
unknown |
Het |
Map3k20 |
A |
T |
2: 72,194,968 (GRCm39) |
|
probably benign |
Het |
Mroh8 |
A |
G |
2: 157,075,125 (GRCm39) |
V457A |
probably benign |
Het |
Mrpl40 |
T |
A |
16: 18,694,159 (GRCm39) |
|
probably null |
Het |
Ms4a10 |
C |
T |
19: 10,941,472 (GRCm39) |
V166I |
probably benign |
Het |
Mycl |
A |
G |
4: 122,894,100 (GRCm39) |
D300G |
probably damaging |
Het |
Naca |
T |
A |
10: 127,879,266 (GRCm39) |
|
probably benign |
Het |
Ncoa4 |
T |
C |
14: 31,895,391 (GRCm39) |
S172P |
probably damaging |
Het |
Nfatc3 |
T |
C |
8: 106,810,486 (GRCm39) |
F421L |
possibly damaging |
Het |
Nucb1 |
C |
A |
7: 45,144,649 (GRCm39) |
K301N |
probably benign |
Het |
Or1af1 |
A |
G |
2: 37,109,966 (GRCm39) |
H155R |
probably damaging |
Het |
Or52ae9 |
A |
T |
7: 103,390,243 (GRCm39) |
M68K |
probably benign |
Het |
Or5b99 |
T |
A |
19: 12,976,815 (GRCm39) |
I155N |
possibly damaging |
Het |
Panx1 |
A |
T |
9: 14,921,341 (GRCm39) |
V178E |
possibly damaging |
Het |
Pkd1l3 |
G |
A |
8: 110,367,402 (GRCm39) |
V1210I |
probably damaging |
Het |
Polr2a |
A |
T |
11: 69,638,039 (GRCm39) |
H143Q |
possibly damaging |
Het |
Potefam1 |
A |
T |
2: 111,048,972 (GRCm39) |
M269K |
probably benign |
Het |
Prdm12 |
G |
A |
2: 31,544,186 (GRCm39) |
R263H |
probably damaging |
Het |
Prkdc |
A |
C |
16: 15,549,430 (GRCm39) |
K1998T |
probably damaging |
Het |
Rab11fip1 |
A |
T |
8: 27,643,051 (GRCm39) |
S583T |
probably damaging |
Het |
Rnf157 |
T |
A |
11: 116,237,921 (GRCm39) |
T567S |
probably benign |
Het |
Rps10 |
A |
C |
17: 27,850,182 (GRCm39) |
F150V |
probably benign |
Het |
Rrp12 |
A |
T |
19: 41,870,639 (GRCm39) |
F499I |
probably damaging |
Het |
Sez6l2 |
G |
A |
7: 126,562,535 (GRCm39) |
R604H |
probably damaging |
Het |
Slc25a21 |
G |
T |
12: 56,904,864 (GRCm39) |
Q57K |
probably benign |
Het |
Slc27a2 |
A |
G |
2: 126,395,234 (GRCm39) |
T54A |
possibly damaging |
Het |
Slc9a9 |
T |
A |
9: 95,111,011 (GRCm39) |
S610T |
probably benign |
Het |
Smc1b |
A |
T |
15: 84,970,335 (GRCm39) |
S973T |
probably benign |
Het |
Smc6 |
G |
A |
12: 11,329,734 (GRCm39) |
S164N |
possibly damaging |
Het |
Sp1 |
A |
G |
15: 102,316,314 (GRCm39) |
T32A |
possibly damaging |
Het |
Spen |
T |
C |
4: 141,202,946 (GRCm39) |
I1894V |
probably benign |
Het |
Spen |
T |
C |
4: 141,203,011 (GRCm39) |
K1872R |
possibly damaging |
Het |
Stab1 |
C |
A |
14: 30,873,541 (GRCm39) |
|
probably benign |
Het |
Taar7d |
T |
G |
10: 23,904,102 (GRCm39) |
F328C |
probably damaging |
Het |
Ticam1 |
A |
T |
17: 56,578,113 (GRCm39) |
S327R |
probably benign |
Het |
Tmem248 |
C |
T |
5: 130,258,295 (GRCm39) |
|
probably benign |
Het |
Tom1 |
T |
C |
8: 75,781,259 (GRCm39) |
S83P |
probably damaging |
Het |
Txk |
T |
A |
5: 72,856,453 (GRCm39) |
Y446F |
probably damaging |
Het |
Ubap1l |
T |
A |
9: 65,279,237 (GRCm39) |
C179S |
probably benign |
Het |
Utrn |
T |
C |
10: 12,331,185 (GRCm39) |
E474G |
possibly damaging |
Het |
Vmn2r14 |
T |
C |
5: 109,363,862 (GRCm39) |
M685V |
probably benign |
Het |
Vmn2r7 |
A |
T |
3: 64,623,881 (GRCm39) |
Y146* |
probably null |
Het |
Wdr1 |
G |
A |
5: 38,697,905 (GRCm39) |
T220M |
probably damaging |
Het |
Xpo7 |
T |
C |
14: 70,915,582 (GRCm39) |
D726G |
probably damaging |
Het |
Zbtb14 |
C |
G |
17: 69,694,759 (GRCm39) |
I152M |
probably benign |
Het |
Zbtb3 |
A |
G |
19: 8,780,771 (GRCm39) |
D128G |
probably damaging |
Het |
Zeb1os1 |
A |
G |
18: 5,583,794 (GRCm39) |
|
noncoding transcript |
Het |
Zfp462 |
T |
A |
4: 55,007,667 (GRCm39) |
D35E |
probably damaging |
Het |
Zfp467 |
A |
G |
6: 48,415,621 (GRCm39) |
S344P |
possibly damaging |
Het |
Zfpm1 |
A |
T |
8: 123,034,285 (GRCm39) |
D73V |
possibly damaging |
Het |
|
Other mutations in Rp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00323:Rp1
|
APN |
1 |
4,416,969 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00593:Rp1
|
APN |
1 |
4,415,626 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL00956:Rp1
|
APN |
1 |
4,422,435 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01070:Rp1
|
APN |
1 |
4,415,461 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01531:Rp1
|
APN |
1 |
4,419,168 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01668:Rp1
|
APN |
1 |
4,415,941 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01907:Rp1
|
APN |
1 |
4,418,730 (GRCm39) |
missense |
possibly damaging |
0.56 |
IGL02055:Rp1
|
APN |
1 |
4,422,745 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02071:Rp1
|
APN |
1 |
4,415,533 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL02128:Rp1
|
APN |
1 |
4,417,608 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02244:Rp1
|
APN |
1 |
4,419,003 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02381:Rp1
|
APN |
1 |
4,422,613 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02499:Rp1
|
APN |
1 |
4,419,271 (GRCm39) |
missense |
probably benign |
0.17 |
IGL02619:Rp1
|
APN |
1 |
4,418,673 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL02832:Rp1
|
APN |
1 |
4,419,936 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02861:Rp1
|
APN |
1 |
4,416,375 (GRCm39) |
nonsense |
probably null |
|
IGL03288:Rp1
|
APN |
1 |
4,419,747 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL03290:Rp1
|
APN |
1 |
4,420,264 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03303:Rp1
|
APN |
1 |
4,415,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R0041:Rp1
|
UTSW |
1 |
4,414,851 (GRCm39) |
missense |
probably benign |
0.36 |
R0111:Rp1
|
UTSW |
1 |
4,414,983 (GRCm39) |
missense |
probably damaging |
1.00 |
R0363:Rp1
|
UTSW |
1 |
4,417,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R0440:Rp1
|
UTSW |
1 |
4,415,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R0442:Rp1
|
UTSW |
1 |
4,416,970 (GRCm39) |
missense |
probably benign |
0.09 |
R0528:Rp1
|
UTSW |
1 |
4,415,088 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0586:Rp1
|
UTSW |
1 |
4,418,060 (GRCm39) |
missense |
possibly damaging |
0.76 |
R0639:Rp1
|
UTSW |
1 |
4,416,721 (GRCm39) |
missense |
probably benign |
0.00 |
R0856:Rp1
|
UTSW |
1 |
4,414,878 (GRCm39) |
missense |
probably benign |
0.05 |
R0908:Rp1
|
UTSW |
1 |
4,414,878 (GRCm39) |
missense |
probably benign |
0.05 |
R0968:Rp1
|
UTSW |
1 |
4,415,575 (GRCm39) |
missense |
probably benign |
0.00 |
R1099:Rp1
|
UTSW |
1 |
4,422,513 (GRCm39) |
missense |
possibly damaging |
0.45 |
R1242:Rp1
|
UTSW |
1 |
4,415,185 (GRCm39) |
missense |
probably benign |
0.03 |
R1301:Rp1
|
UTSW |
1 |
4,416,159 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1327:Rp1
|
UTSW |
1 |
4,418,193 (GRCm39) |
missense |
probably benign |
0.01 |
R1403:Rp1
|
UTSW |
1 |
4,416,520 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1403:Rp1
|
UTSW |
1 |
4,416,520 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1406:Rp1
|
UTSW |
1 |
4,422,144 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1406:Rp1
|
UTSW |
1 |
4,422,144 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1440:Rp1
|
UTSW |
1 |
4,417,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R1509:Rp1
|
UTSW |
1 |
4,417,917 (GRCm39) |
missense |
probably damaging |
0.98 |
R1538:Rp1
|
UTSW |
1 |
4,415,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R1609:Rp1
|
UTSW |
1 |
4,419,424 (GRCm39) |
missense |
probably damaging |
1.00 |
R1666:Rp1
|
UTSW |
1 |
4,420,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R1703:Rp1
|
UTSW |
1 |
4,415,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R1782:Rp1
|
UTSW |
1 |
4,419,312 (GRCm39) |
missense |
probably benign |
0.00 |
R1799:Rp1
|
UTSW |
1 |
4,419,055 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1848:Rp1
|
UTSW |
1 |
4,417,455 (GRCm39) |
missense |
possibly damaging |
0.76 |
R1908:Rp1
|
UTSW |
1 |
4,418,943 (GRCm39) |
missense |
probably damaging |
0.99 |
R1919:Rp1
|
UTSW |
1 |
4,422,894 (GRCm39) |
missense |
probably damaging |
0.99 |
R2087:Rp1
|
UTSW |
1 |
4,418,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R2211:Rp1
|
UTSW |
1 |
4,418,362 (GRCm39) |
missense |
probably damaging |
0.96 |
R2278:Rp1
|
UTSW |
1 |
4,418,250 (GRCm39) |
missense |
possibly damaging |
0.51 |
R2287:Rp1
|
UTSW |
1 |
4,416,182 (GRCm39) |
nonsense |
probably null |
|
R2316:Rp1
|
UTSW |
1 |
4,415,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R2346:Rp1
|
UTSW |
1 |
4,418,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R2878:Rp1
|
UTSW |
1 |
4,418,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R3023:Rp1
|
UTSW |
1 |
4,422,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R3025:Rp1
|
UTSW |
1 |
4,422,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R3716:Rp1
|
UTSW |
1 |
4,419,988 (GRCm39) |
missense |
probably benign |
0.38 |
R3814:Rp1
|
UTSW |
1 |
4,419,931 (GRCm39) |
missense |
probably benign |
|
R3929:Rp1
|
UTSW |
1 |
4,422,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R4064:Rp1
|
UTSW |
1 |
4,415,623 (GRCm39) |
missense |
probably benign |
0.08 |
R4426:Rp1
|
UTSW |
1 |
4,418,147 (GRCm39) |
missense |
probably benign |
0.13 |
R4557:Rp1
|
UTSW |
1 |
4,414,886 (GRCm39) |
missense |
possibly damaging |
0.61 |
R4764:Rp1
|
UTSW |
1 |
4,416,101 (GRCm39) |
missense |
probably damaging |
0.96 |
R4845:Rp1
|
UTSW |
1 |
4,419,451 (GRCm39) |
missense |
probably benign |
0.02 |
R4850:Rp1
|
UTSW |
1 |
4,418,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R4857:Rp1
|
UTSW |
1 |
4,422,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R4857:Rp1
|
UTSW |
1 |
4,422,539 (GRCm39) |
missense |
probably damaging |
0.99 |
R5159:Rp1
|
UTSW |
1 |
4,416,426 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5226:Rp1
|
UTSW |
1 |
4,418,256 (GRCm39) |
missense |
probably benign |
0.01 |
R5327:Rp1
|
UTSW |
1 |
4,419,583 (GRCm39) |
splice site |
probably null |
|
R5352:Rp1
|
UTSW |
1 |
4,417,321 (GRCm39) |
missense |
probably benign |
0.00 |
R5504:Rp1
|
UTSW |
1 |
4,420,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R5527:Rp1
|
UTSW |
1 |
4,416,616 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5529:Rp1
|
UTSW |
1 |
4,416,055 (GRCm39) |
missense |
probably benign |
0.42 |
R5569:Rp1
|
UTSW |
1 |
4,415,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R5622:Rp1
|
UTSW |
1 |
4,418,060 (GRCm39) |
missense |
possibly damaging |
0.76 |
R5970:Rp1
|
UTSW |
1 |
4,418,685 (GRCm39) |
missense |
probably benign |
0.05 |
R5992:Rp1
|
UTSW |
1 |
4,218,926 (GRCm39) |
missense |
unknown |
|
R6004:Rp1
|
UTSW |
1 |
4,267,808 (GRCm39) |
missense |
unknown |
|
R6018:Rp1
|
UTSW |
1 |
4,423,059 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6074:Rp1
|
UTSW |
1 |
4,415,602 (GRCm39) |
missense |
probably benign |
0.02 |
R6127:Rp1
|
UTSW |
1 |
4,419,534 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6187:Rp1
|
UTSW |
1 |
4,420,092 (GRCm39) |
missense |
probably damaging |
1.00 |
R6301:Rp1
|
UTSW |
1 |
4,417,477 (GRCm39) |
missense |
probably benign |
0.04 |
R6317:Rp1
|
UTSW |
1 |
4,112,212 (GRCm39) |
missense |
unknown |
|
R6405:Rp1
|
UTSW |
1 |
4,415,994 (GRCm39) |
missense |
probably damaging |
1.00 |
R6445:Rp1
|
UTSW |
1 |
4,296,840 (GRCm39) |
missense |
unknown |
|
R6466:Rp1
|
UTSW |
1 |
4,418,109 (GRCm39) |
missense |
probably benign |
0.01 |
R6501:Rp1
|
UTSW |
1 |
4,381,503 (GRCm39) |
intron |
probably benign |
|
R6547:Rp1
|
UTSW |
1 |
4,240,528 (GRCm39) |
missense |
unknown |
|
R6604:Rp1
|
UTSW |
1 |
4,089,351 (GRCm39) |
missense |
unknown |
|
R6700:Rp1
|
UTSW |
1 |
4,420,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R6706:Rp1
|
UTSW |
1 |
4,212,887 (GRCm39) |
missense |
unknown |
|
R6831:Rp1
|
UTSW |
1 |
4,420,087 (GRCm39) |
splice site |
probably null |
|
R6918:Rp1
|
UTSW |
1 |
4,069,831 (GRCm39) |
missense |
unknown |
|
R6973:Rp1
|
UTSW |
1 |
4,422,217 (GRCm39) |
nonsense |
probably null |
|
R6981:Rp1
|
UTSW |
1 |
4,415,878 (GRCm39) |
missense |
probably benign |
0.06 |
R7009:Rp1
|
UTSW |
1 |
4,112,291 (GRCm39) |
missense |
unknown |
|
R7078:Rp1
|
UTSW |
1 |
4,277,014 (GRCm39) |
missense |
unknown |
|
R7112:Rp1
|
UTSW |
1 |
4,419,241 (GRCm39) |
missense |
probably benign |
0.43 |
R7135:Rp1
|
UTSW |
1 |
4,418,391 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7165:Rp1
|
UTSW |
1 |
4,420,140 (GRCm39) |
missense |
probably damaging |
0.99 |
R7199:Rp1
|
UTSW |
1 |
4,417,513 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7232:Rp1
|
UTSW |
1 |
4,298,824 (GRCm39) |
missense |
unknown |
|
R7367:Rp1
|
UTSW |
1 |
4,418,221 (GRCm39) |
missense |
probably benign |
0.42 |
R7484:Rp1
|
UTSW |
1 |
4,415,704 (GRCm39) |
missense |
probably benign |
0.10 |
R7500:Rp1
|
UTSW |
1 |
4,381,501 (GRCm39) |
missense |
unknown |
|
R7569:Rp1
|
UTSW |
1 |
4,355,063 (GRCm39) |
missense |
unknown |
|
R7642:Rp1
|
UTSW |
1 |
4,218,054 (GRCm39) |
missense |
unknown |
|
R7693:Rp1
|
UTSW |
1 |
4,417,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R7742:Rp1
|
UTSW |
1 |
4,240,457 (GRCm39) |
missense |
unknown |
|
R7759:Rp1
|
UTSW |
1 |
4,415,107 (GRCm39) |
missense |
probably benign |
|
R7784:Rp1
|
UTSW |
1 |
4,212,881 (GRCm39) |
missense |
unknown |
|
R7816:Rp1
|
UTSW |
1 |
4,417,926 (GRCm39) |
missense |
probably damaging |
0.98 |
R7866:Rp1
|
UTSW |
1 |
4,417,924 (GRCm39) |
missense |
probably benign |
0.02 |
R8215:Rp1
|
UTSW |
1 |
4,315,318 (GRCm39) |
missense |
unknown |
|
R8281:Rp1
|
UTSW |
1 |
4,418,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R8294:Rp1
|
UTSW |
1 |
4,416,220 (GRCm39) |
missense |
probably benign |
0.09 |
R8309:Rp1
|
UTSW |
1 |
4,417,312 (GRCm39) |
missense |
probably benign |
0.00 |
R8311:Rp1
|
UTSW |
1 |
4,418,572 (GRCm39) |
missense |
probably benign |
0.11 |
R8500:Rp1
|
UTSW |
1 |
4,416,813 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8559:Rp1
|
UTSW |
1 |
4,419,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R8672:Rp1
|
UTSW |
1 |
4,419,007 (GRCm39) |
missense |
possibly damaging |
0.55 |
R8688:Rp1
|
UTSW |
1 |
4,416,628 (GRCm39) |
missense |
probably benign |
0.01 |
R8792:Rp1
|
UTSW |
1 |
4,095,091 (GRCm39) |
missense |
unknown |
|
R8859:Rp1
|
UTSW |
1 |
4,420,183 (GRCm39) |
missense |
probably benign |
0.07 |
R8945:Rp1
|
UTSW |
1 |
4,419,817 (GRCm39) |
missense |
probably benign |
0.42 |
R8959:Rp1
|
UTSW |
1 |
4,419,650 (GRCm39) |
intron |
probably benign |
|
R8979:Rp1
|
UTSW |
1 |
4,218,937 (GRCm39) |
missense |
unknown |
|
R9126:Rp1
|
UTSW |
1 |
4,417,136 (GRCm39) |
missense |
probably damaging |
0.99 |
R9156:Rp1
|
UTSW |
1 |
4,234,161 (GRCm39) |
missense |
unknown |
|
R9160:Rp1
|
UTSW |
1 |
4,416,720 (GRCm39) |
missense |
probably benign |
0.00 |
R9221:Rp1
|
UTSW |
1 |
4,315,266 (GRCm39) |
missense |
unknown |
|
R9263:Rp1
|
UTSW |
1 |
4,419,160 (GRCm39) |
missense |
probably benign |
0.02 |
R9263:Rp1
|
UTSW |
1 |
4,418,675 (GRCm39) |
missense |
probably benign |
0.25 |
R9302:Rp1
|
UTSW |
1 |
4,416,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R9318:Rp1
|
UTSW |
1 |
4,418,488 (GRCm39) |
missense |
probably benign |
0.09 |
R9414:Rp1
|
UTSW |
1 |
4,313,841 (GRCm39) |
missense |
unknown |
|
R9474:Rp1
|
UTSW |
1 |
4,162,838 (GRCm39) |
critical splice donor site |
probably null |
|
R9478:Rp1
|
UTSW |
1 |
4,417,545 (GRCm39) |
missense |
probably benign |
0.06 |
R9529:Rp1
|
UTSW |
1 |
4,416,447 (GRCm39) |
missense |
probably benign |
|
R9572:Rp1
|
UTSW |
1 |
4,418,662 (GRCm39) |
missense |
probably benign |
|
R9673:Rp1
|
UTSW |
1 |
4,337,792 (GRCm39) |
missense |
unknown |
|
R9709:Rp1
|
UTSW |
1 |
4,112,255 (GRCm39) |
missense |
unknown |
|
R9716:Rp1
|
UTSW |
1 |
4,212,833 (GRCm39) |
critical splice donor site |
probably null |
|
RF003:Rp1
|
UTSW |
1 |
4,414,917 (GRCm39) |
missense |
probably damaging |
0.99 |
V1662:Rp1
|
UTSW |
1 |
4,419,783 (GRCm39) |
missense |
probably damaging |
1.00 |
X0012:Rp1
|
UTSW |
1 |
4,417,918 (GRCm39) |
missense |
probably damaging |
0.96 |
|