Other mutations in this stock |
Total: 91 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acaca |
G |
A |
11: 84,154,138 (GRCm39) |
R953Q |
possibly damaging |
Het |
Aldh1a1 |
A |
T |
19: 20,579,434 (GRCm39) |
H20L |
probably benign |
Het |
Ankrd52 |
T |
A |
10: 128,219,526 (GRCm39) |
C487S |
probably benign |
Het |
Ap1s3 |
T |
C |
1: 79,602,845 (GRCm39) |
E54G |
probably benign |
Het |
Arglu1 |
A |
C |
8: 8,717,361 (GRCm39) |
M236R |
probably benign |
Het |
Baz1b |
T |
A |
5: 135,246,293 (GRCm39) |
F581I |
probably benign |
Het |
Bbox1 |
T |
G |
2: 110,122,884 (GRCm39) |
D135A |
probably benign |
Het |
Bcl2l14 |
T |
A |
6: 134,400,786 (GRCm39) |
V69E |
probably damaging |
Het |
Brinp3 |
C |
T |
1: 146,390,627 (GRCm39) |
Q58* |
probably null |
Het |
Ccnb1ip1 |
T |
A |
14: 51,029,724 (GRCm39) |
K113* |
probably null |
Het |
Cep128 |
T |
C |
12: 91,200,878 (GRCm39) |
I830M |
probably damaging |
Het |
Ces2f |
C |
T |
8: 105,681,284 (GRCm39) |
T541I |
probably damaging |
Het |
Chsy3 |
C |
A |
18: 59,309,149 (GRCm39) |
P134Q |
possibly damaging |
Het |
Cobl |
T |
G |
11: 12,328,271 (GRCm39) |
T112P |
probably damaging |
Het |
Cplane2 |
A |
T |
4: 140,947,159 (GRCm39) |
Y180F |
probably benign |
Het |
Dcc |
T |
A |
18: 71,680,469 (GRCm39) |
K589I |
probably benign |
Het |
Depdc1b |
T |
A |
13: 108,523,505 (GRCm39) |
I460K |
possibly damaging |
Het |
Dlst |
T |
C |
12: 85,157,705 (GRCm39) |
F12S |
probably benign |
Het |
Dnah1 |
G |
C |
14: 31,019,067 (GRCm39) |
F1342L |
probably damaging |
Het |
Dtnb |
A |
G |
12: 3,798,480 (GRCm39) |
Q438R |
possibly damaging |
Het |
Dusp4 |
C |
A |
8: 35,275,065 (GRCm39) |
S61R |
probably damaging |
Het |
E130308A19Rik |
A |
G |
4: 59,737,688 (GRCm39) |
Y433C |
probably damaging |
Het |
Ebf2 |
T |
C |
14: 67,661,407 (GRCm39) |
S512P |
probably benign |
Het |
Elapor2 |
A |
G |
5: 9,460,709 (GRCm39) |
N210S |
probably benign |
Het |
Eya1 |
C |
T |
1: 14,301,636 (GRCm39) |
|
probably null |
Het |
Fsd1 |
G |
A |
17: 56,300,876 (GRCm39) |
R245H |
probably damaging |
Het |
Fzr1 |
T |
A |
10: 81,204,463 (GRCm39) |
D379V |
probably damaging |
Het |
Gk2 |
T |
A |
5: 97,604,195 (GRCm39) |
E214D |
probably benign |
Het |
Gm10837 |
C |
G |
14: 122,728,142 (GRCm39) |
A6G |
unknown |
Het |
Gmnc |
A |
T |
16: 26,779,272 (GRCm39) |
V251E |
probably benign |
Het |
Golga3 |
A |
G |
5: 110,340,953 (GRCm39) |
Q549R |
probably damaging |
Het |
Gsdmd |
T |
G |
15: 75,736,204 (GRCm39) |
V111G |
probably damaging |
Het |
Gtf3c1 |
T |
C |
7: 125,244,914 (GRCm39) |
T1707A |
possibly damaging |
Het |
Gucy2c |
C |
T |
6: 136,674,937 (GRCm39) |
V1049M |
probably benign |
Het |
Gucy2g |
A |
G |
19: 55,229,583 (GRCm39) |
V29A |
probably damaging |
Het |
Hecw1 |
A |
T |
13: 14,609,044 (GRCm39) |
M1K |
probably null |
Het |
Hmcn1 |
T |
C |
1: 150,736,118 (GRCm39) |
D117G |
probably damaging |
Het |
Ifnab |
T |
A |
4: 88,609,350 (GRCm39) |
T39S |
possibly damaging |
Het |
Lcorl |
A |
G |
5: 45,904,566 (GRCm39) |
Y171H |
probably damaging |
Het |
Ly6g6c |
C |
T |
17: 35,288,437 (GRCm39) |
P103L |
probably damaging |
Het |
Macf1 |
T |
G |
4: 123,325,936 (GRCm39) |
E5189A |
probably damaging |
Het |
Mapkap1 |
A |
G |
2: 34,453,151 (GRCm39) |
E348G |
probably damaging |
Het |
Med25 |
G |
T |
7: 44,534,325 (GRCm39) |
A280D |
probably damaging |
Het |
Mep1b |
C |
A |
18: 21,233,108 (GRCm39) |
A703E |
probably benign |
Het |
Morn5 |
T |
A |
2: 35,944,990 (GRCm39) |
N71K |
probably benign |
Het |
Mtmr10 |
T |
A |
7: 63,970,375 (GRCm39) |
Y373N |
possibly damaging |
Het |
Myo1d |
C |
T |
11: 80,565,460 (GRCm39) |
E426K |
probably damaging |
Het |
Ncbp1 |
G |
C |
4: 46,155,756 (GRCm39) |
V302L |
probably benign |
Het |
Notch4 |
A |
G |
17: 34,801,520 (GRCm39) |
T1123A |
possibly damaging |
Het |
Nudt18 |
T |
A |
14: 70,816,452 (GRCm39) |
M88K |
possibly damaging |
Het |
Or12k8 |
A |
G |
2: 36,975,608 (GRCm39) |
S51P |
possibly damaging |
Het |
Or5b100-ps1 |
A |
T |
19: 12,994,097 (GRCm39) |
D170V |
possibly damaging |
Het |
Or6d12 |
T |
A |
6: 116,493,632 (GRCm39) |
L298Q |
probably damaging |
Het |
Or8g4 |
A |
T |
9: 39,661,787 (GRCm39) |
Y35F |
possibly damaging |
Het |
Pdcd6ip |
T |
C |
9: 113,488,953 (GRCm39) |
N694S |
probably benign |
Het |
Pecam1 |
T |
A |
11: 106,579,773 (GRCm39) |
T430S |
probably benign |
Het |
Plaa |
T |
G |
4: 94,462,288 (GRCm39) |
T530P |
probably benign |
Het |
Ppfia3 |
G |
T |
7: 45,010,019 (GRCm39) |
Q95K |
probably damaging |
Het |
Ppp4r2 |
T |
C |
6: 100,843,274 (GRCm39) |
S331P |
probably benign |
Het |
Prg4 |
T |
C |
1: 150,334,014 (GRCm39) |
T117A |
possibly damaging |
Het |
Prrc2b |
A |
T |
2: 32,103,531 (GRCm39) |
D1003V |
probably benign |
Het |
Ptk2 |
G |
A |
15: 73,093,658 (GRCm39) |
P854S |
possibly damaging |
Het |
Rasef |
T |
C |
4: 73,698,626 (GRCm39) |
I12V |
probably benign |
Het |
Robo2 |
T |
G |
16: 74,149,504 (GRCm39) |
Y108S |
probably damaging |
Het |
Rsrc1 |
T |
C |
3: 66,901,987 (GRCm39) |
S46P |
unknown |
Het |
Rttn |
A |
T |
18: 89,027,546 (GRCm39) |
T554S |
probably benign |
Het |
Sall3 |
C |
T |
18: 81,017,314 (GRCm39) |
V205M |
probably damaging |
Het |
Scn3a |
C |
A |
2: 65,327,944 (GRCm39) |
V849L |
probably damaging |
Het |
Sec23a |
A |
G |
12: 59,039,069 (GRCm39) |
C277R |
probably benign |
Het |
Sf3b3 |
C |
T |
8: 111,539,639 (GRCm39) |
A1075T |
possibly damaging |
Het |
Sfxn5 |
T |
C |
6: 85,309,366 (GRCm39) |
D113G |
unknown |
Het |
Slc22a22 |
C |
T |
15: 57,126,876 (GRCm39) |
M64I |
probably benign |
Het |
Slc5a11 |
C |
T |
7: 122,857,669 (GRCm39) |
P253S |
probably damaging |
Het |
Smarcd3 |
A |
G |
5: 24,798,067 (GRCm39) |
F449S |
probably damaging |
Het |
Sspo |
C |
T |
6: 48,437,313 (GRCm39) |
T1357M |
probably damaging |
Het |
Styx |
C |
T |
14: 45,609,873 (GRCm39) |
T179I |
probably benign |
Het |
Syt7 |
A |
T |
19: 10,412,963 (GRCm39) |
T297S |
probably benign |
Het |
Tbx19 |
T |
A |
1: 164,988,135 (GRCm39) |
|
probably benign |
Het |
Tg |
T |
A |
15: 66,545,392 (GRCm39) |
V149E |
probably damaging |
Het |
Tgfbr3l |
T |
A |
8: 4,299,238 (GRCm39) |
L35Q |
probably damaging |
Het |
Tmem161b |
C |
A |
13: 84,370,537 (GRCm39) |
|
probably benign |
Het |
Tmem219 |
T |
A |
7: 126,490,975 (GRCm39) |
T161S |
probably damaging |
Het |
Tox2 |
T |
A |
2: 163,162,501 (GRCm39) |
L68H |
|
Het |
Trim5 |
T |
A |
7: 103,927,681 (GRCm39) |
D153V |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,580,651 (GRCm39) |
Y23414C |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,582,153 (GRCm39) |
N22913K |
probably damaging |
Het |
Ubr2 |
A |
C |
17: 47,266,779 (GRCm39) |
M1124R |
possibly damaging |
Het |
Vmn2r75 |
A |
G |
7: 85,815,568 (GRCm39) |
S99P |
probably damaging |
Het |
Wdr83 |
T |
C |
8: 85,802,680 (GRCm39) |
D219G |
probably damaging |
Het |
Wdr90 |
C |
T |
17: 26,068,623 (GRCm39) |
V1285M |
probably damaging |
Het |
Zmynd15 |
A |
T |
11: 70,351,581 (GRCm39) |
L62F |
probably 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 |
4,418,760 (GRCm39) |
missense |
probably benign |
0.20 |
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 |
|
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 |
|