Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930568D16Rik |
T |
C |
2: 35,244,399 (GRCm39) |
K318E |
probably benign |
Het |
Ap5z1 |
T |
C |
5: 142,463,113 (GRCm39) |
F766L |
probably benign |
Het |
Atrnl1 |
A |
G |
19: 57,599,786 (GRCm39) |
M1V |
probably null |
Het |
Atxn1 |
T |
C |
13: 45,710,622 (GRCm39) |
E770G |
probably benign |
Het |
Brwd1 |
T |
G |
16: 95,813,096 (GRCm39) |
I1471L |
probably benign |
Het |
Bud23 |
T |
C |
5: 135,082,571 (GRCm39) |
E66G |
probably benign |
Het |
Cdh8 |
T |
A |
8: 99,757,367 (GRCm39) |
I744L |
possibly damaging |
Het |
Celsr1 |
G |
T |
15: 85,917,286 (GRCm39) |
S229* |
probably null |
Het |
Cep95 |
C |
A |
11: 106,703,322 (GRCm39) |
H467Q |
probably benign |
Het |
Chd1 |
A |
G |
17: 15,989,023 (GRCm39) |
Y1592C |
probably benign |
Het |
Chkb |
C |
G |
15: 89,313,628 (GRCm39) |
G59A |
probably damaging |
Het |
Copa |
A |
G |
1: 171,945,648 (GRCm39) |
S915G |
probably benign |
Het |
Creb3 |
G |
T |
4: 43,563,191 (GRCm39) |
V97F |
probably damaging |
Het |
Csmd2 |
T |
A |
4: 128,308,062 (GRCm39) |
H1273Q |
|
Het |
Cxcr1 |
T |
C |
1: 74,231,074 (GRCm39) |
N316S |
probably benign |
Het |
Cyct |
A |
T |
2: 76,184,523 (GRCm39) |
I76N |
probably damaging |
Het |
Dmxl2 |
G |
T |
9: 54,294,840 (GRCm39) |
R2412S |
probably damaging |
Het |
Dnah11 |
A |
G |
12: 117,982,513 (GRCm39) |
M2552T |
possibly damaging |
Het |
Dnph1 |
G |
A |
17: 46,809,901 (GRCm39) |
E148K |
possibly damaging |
Het |
Ecpas |
T |
C |
4: 58,822,060 (GRCm39) |
N1169S |
probably benign |
Het |
Esp16 |
T |
A |
17: 39,848,731 (GRCm39) |
Y8* |
probably null |
Het |
Fam186a |
T |
C |
15: 99,841,024 (GRCm39) |
D1740G |
possibly damaging |
Het |
Fam76a |
C |
A |
4: 132,628,557 (GRCm39) |
K300N |
probably damaging |
Het |
Fcgbpl1 |
A |
G |
7: 27,856,044 (GRCm39) |
T1944A |
probably benign |
Het |
Frrs1l |
A |
C |
4: 56,990,191 (GRCm39) |
D27E |
|
Het |
G6pc1 |
T |
C |
11: 101,267,380 (GRCm39) |
S277P |
probably damaging |
Het |
Gabrg3 |
T |
A |
7: 56,973,422 (GRCm39) |
I82F |
probably damaging |
Het |
Gm3604 |
G |
T |
13: 62,517,969 (GRCm39) |
Q130K |
probably benign |
Het |
Hhip |
T |
A |
8: 80,719,108 (GRCm39) |
D473V |
probably damaging |
Het |
Ifi209 |
T |
C |
1: 173,470,332 (GRCm39) |
S307P |
probably damaging |
Het |
Ino80c |
C |
T |
18: 24,254,856 (GRCm39) |
M1I |
probably null |
Het |
Jag2 |
G |
T |
12: 112,875,416 (GRCm39) |
C872* |
probably null |
Het |
Kcnma1 |
A |
C |
14: 23,558,123 (GRCm39) |
H474Q |
probably benign |
Het |
Krr1 |
G |
A |
10: 111,818,963 (GRCm39) |
|
probably null |
Het |
Lats1 |
T |
G |
10: 7,588,387 (GRCm39) |
D1001E |
probably benign |
Het |
Lilrb4b |
T |
C |
10: 51,357,753 (GRCm39) |
L149P |
probably benign |
Het |
Lrrk2 |
T |
A |
15: 91,649,884 (GRCm39) |
S1674T |
probably damaging |
Het |
Magi2 |
A |
G |
5: 20,670,582 (GRCm39) |
I309V |
possibly damaging |
Het |
Mtmr4 |
T |
C |
11: 87,504,916 (GRCm39) |
V1137A |
probably damaging |
Het |
Mtmr4 |
A |
G |
11: 87,503,138 (GRCm39) |
D1064G |
probably damaging |
Het |
Neb |
C |
T |
2: 52,133,853 (GRCm39) |
|
probably null |
Het |
Nhsl1 |
T |
A |
10: 18,402,665 (GRCm39) |
V1297E |
possibly damaging |
Het |
Nlrp3 |
T |
A |
11: 59,440,148 (GRCm39) |
V575D |
probably damaging |
Het |
Nptx2 |
T |
C |
5: 144,492,159 (GRCm39) |
I312T |
possibly damaging |
Het |
Osm |
A |
G |
11: 4,189,926 (GRCm39) |
T237A |
probably benign |
Het |
Pcdha12 |
T |
C |
18: 37,155,234 (GRCm39) |
V651A |
possibly damaging |
Het |
Pclo |
A |
G |
5: 14,908,758 (GRCm39) |
|
probably null |
Het |
Pdlim3 |
C |
T |
8: 46,368,195 (GRCm39) |
S183L |
possibly damaging |
Het |
Peg10 |
GC |
GCTCC |
6: 4,756,452 (GRCm39) |
|
probably benign |
Het |
Pgm2 |
T |
A |
5: 64,273,671 (GRCm39) |
M552K |
probably damaging |
Het |
Pkhd1l1 |
T |
C |
15: 44,386,901 (GRCm39) |
L1258S |
probably benign |
Het |
Proser3 |
T |
G |
7: 30,248,530 (GRCm39) |
T55P |
probably damaging |
Het |
Ranbp2 |
C |
A |
10: 58,300,963 (GRCm39) |
P611Q |
probably damaging |
Het |
Rangap1 |
T |
C |
15: 81,590,637 (GRCm39) |
D485G |
probably benign |
Het |
Ryr3 |
G |
A |
2: 112,486,883 (GRCm39) |
L3862F |
possibly damaging |
Het |
Sbf1 |
C |
T |
15: 89,179,675 (GRCm39) |
G1337R |
possibly damaging |
Het |
Setd2 |
A |
G |
9: 110,378,138 (GRCm39) |
E651G |
probably damaging |
Het |
Shmt1 |
A |
G |
11: 60,692,769 (GRCm39) |
W105R |
probably damaging |
Het |
Skor2 |
C |
T |
18: 76,946,376 (GRCm39) |
H33Y |
unknown |
Het |
Slc22a29 |
T |
C |
19: 8,140,104 (GRCm39) |
I434V |
probably benign |
Het |
Sord |
C |
T |
2: 122,090,712 (GRCm39) |
T221I |
probably benign |
Het |
Speer1g |
T |
A |
5: 11,178,990 (GRCm39) |
N55K |
probably benign |
Het |
Tbcd |
T |
C |
11: 121,464,647 (GRCm39) |
Y561H |
probably damaging |
Het |
Tcaf1 |
G |
A |
6: 42,663,808 (GRCm39) |
S24F |
probably benign |
Het |
Tenm4 |
A |
T |
7: 96,517,196 (GRCm39) |
D1429V |
probably damaging |
Het |
Tesk1 |
A |
G |
4: 43,444,574 (GRCm39) |
Y126C |
probably damaging |
Het |
Tmem176a |
G |
A |
6: 48,820,952 (GRCm39) |
V141I |
probably benign |
Het |
Tmem204 |
A |
T |
17: 25,299,243 (GRCm39) |
V92D |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,572,605 (GRCm39) |
D26096V |
probably damaging |
Het |
Vmn1r70 |
T |
A |
7: 10,368,364 (GRCm39) |
L284Q |
probably damaging |
Het |
Vmn2r77 |
T |
C |
7: 86,450,171 (GRCm39) |
V139A |
possibly damaging |
Het |
Wdpcp |
A |
G |
11: 21,671,285 (GRCm39) |
R509G |
possibly damaging |
Het |
Wee1 |
C |
T |
7: 109,725,210 (GRCm39) |
T284I |
probably damaging |
Het |
Wfs1 |
A |
G |
5: 37,125,113 (GRCm39) |
S593P |
probably damaging |
Het |
Zbtb11 |
A |
G |
16: 55,827,336 (GRCm39) |
H934R |
probably damaging |
Het |
Zfp277 |
A |
T |
12: 40,370,611 (GRCm39) |
V446E |
probably benign |
Het |
Zfp874a |
C |
A |
13: 67,591,156 (GRCm39) |
R176L |
probably benign |
Het |
Znrf2 |
A |
T |
6: 54,840,978 (GRCm39) |
N184I |
probably damaging |
Het |
Zp2 |
T |
A |
7: 119,733,238 (GRCm39) |
T568S |
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 |
|
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 |
|
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 |
|