Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700066M21Rik |
T |
A |
1: 57,422,474 (GRCm39) |
H283Q |
probably damaging |
Het |
2810021J22Rik |
A |
G |
11: 58,767,595 (GRCm39) |
K31E |
probably damaging |
Het |
Abcc10 |
G |
C |
17: 46,614,491 (GRCm39) |
N1477K |
probably benign |
Het |
Adam33 |
T |
C |
2: 130,897,266 (GRCm39) |
T310A |
probably benign |
Het |
Afm |
A |
G |
5: 90,671,594 (GRCm39) |
D92G |
probably benign |
Het |
Arg1 |
C |
T |
10: 24,798,561 (GRCm39) |
A30T |
probably benign |
Het |
Ash1l |
C |
G |
3: 88,873,510 (GRCm39) |
P98A |
probably damaging |
Het |
Atad5 |
A |
T |
11: 79,988,878 (GRCm39) |
|
probably null |
Het |
Atg2a |
T |
C |
19: 6,307,488 (GRCm39) |
V1474A |
probably benign |
Het |
Atp12a |
A |
G |
14: 56,603,466 (GRCm39) |
K24E |
probably benign |
Het |
Auh |
G |
A |
13: 52,989,532 (GRCm39) |
P308L |
probably benign |
Het |
B3gnt4 |
A |
T |
5: 123,649,433 (GRCm39) |
H266L |
probably benign |
Het |
Bora |
T |
C |
14: 99,299,714 (GRCm39) |
S229P |
probably damaging |
Het |
Ccn1 |
C |
T |
3: 145,354,428 (GRCm39) |
W161* |
probably null |
Het |
Cdsn |
A |
T |
17: 35,865,591 (GRCm39) |
D40V |
probably damaging |
Het |
Cep295 |
T |
C |
9: 15,252,860 (GRCm39) |
R323G |
probably damaging |
Het |
Chek2 |
T |
C |
5: 110,989,112 (GRCm39) |
|
probably benign |
Het |
Chga |
A |
T |
12: 102,529,122 (GRCm39) |
K366N |
probably damaging |
Het |
Chrm5 |
T |
C |
2: 112,309,572 (GRCm39) |
K515E |
probably null |
Het |
Cmtr1 |
A |
G |
17: 29,913,757 (GRCm39) |
|
probably null |
Het |
Dsg3 |
T |
C |
18: 20,669,882 (GRCm39) |
L632S |
probably damaging |
Het |
Eif1ad8 |
T |
A |
12: 87,563,822 (GRCm39) |
F52L |
probably benign |
Het |
Fzd3 |
A |
G |
14: 65,473,012 (GRCm39) |
F252S |
probably damaging |
Het |
Gas2l2 |
T |
C |
11: 83,312,775 (GRCm39) |
K846E |
probably benign |
Het |
Gpatch11 |
T |
C |
17: 79,148,514 (GRCm39) |
|
probably null |
Het |
Gucy2g |
T |
A |
19: 55,210,772 (GRCm39) |
Y661F |
possibly damaging |
Het |
Hhip |
A |
G |
8: 80,783,931 (GRCm39) |
F72L |
probably benign |
Het |
Kat14 |
T |
C |
2: 144,231,136 (GRCm39) |
L181P |
probably damaging |
Het |
Kifc3 |
A |
T |
8: 95,834,981 (GRCm39) |
|
probably null |
Het |
Kntc1 |
G |
T |
5: 123,932,340 (GRCm39) |
|
probably null |
Het |
Man2b1 |
G |
T |
8: 85,812,013 (GRCm39) |
V156L |
possibly damaging |
Het |
Mast1 |
T |
C |
8: 85,647,823 (GRCm39) |
D517G |
probably damaging |
Het |
Mc1r |
T |
C |
8: 124,135,108 (GRCm39) |
L287P |
possibly damaging |
Het |
Mctp1 |
A |
T |
13: 76,907,843 (GRCm39) |
E238V |
probably damaging |
Het |
Mmp12 |
T |
A |
9: 7,349,725 (GRCm39) |
I52N |
probably damaging |
Het |
Morc1 |
C |
T |
16: 48,412,974 (GRCm39) |
T705I |
probably benign |
Het |
Mrpl24 |
T |
C |
3: 87,830,374 (GRCm39) |
|
probably null |
Het |
Nap1l1 |
C |
T |
10: 111,328,761 (GRCm39) |
T230I |
possibly damaging |
Het |
Niban1 |
T |
C |
1: 151,512,181 (GRCm39) |
F28L |
probably damaging |
Het |
Nmral1 |
T |
A |
16: 4,534,211 (GRCm39) |
I77F |
probably damaging |
Het |
Nudt13 |
T |
A |
14: 20,354,045 (GRCm39) |
D36E |
probably damaging |
Het |
Oxsm |
A |
G |
14: 16,241,983 (GRCm38) |
L262P |
probably benign |
Het |
Pde10a |
A |
T |
17: 9,180,827 (GRCm39) |
I754F |
probably benign |
Het |
Pdzph1 |
T |
C |
17: 59,281,092 (GRCm39) |
R397G |
probably benign |
Het |
Pgap6 |
T |
C |
17: 26,341,017 (GRCm39) |
Y176H |
probably damaging |
Het |
Polr1a |
T |
A |
6: 71,953,058 (GRCm39) |
V567E |
possibly damaging |
Het |
Pou3f2 |
A |
G |
4: 22,488,076 (GRCm39) |
V19A |
probably benign |
Het |
Pramel34 |
T |
G |
5: 93,784,375 (GRCm39) |
Q363P |
probably damaging |
Het |
Pth1r |
A |
G |
9: 110,556,081 (GRCm39) |
I264T |
probably benign |
Het |
Ptprn |
C |
A |
1: 75,231,788 (GRCm39) |
G504C |
probably damaging |
Het |
Rbak |
A |
G |
5: 143,162,339 (GRCm39) |
L8P |
probably damaging |
Het |
Rhob |
A |
G |
12: 8,549,232 (GRCm39) |
M134T |
probably benign |
Het |
Slc10a4 |
T |
C |
5: 73,164,840 (GRCm39) |
L144P |
probably damaging |
Het |
Slc45a3 |
T |
C |
1: 131,905,370 (GRCm39) |
L131P |
probably damaging |
Het |
Slf1 |
T |
A |
13: 77,252,743 (GRCm39) |
E259D |
probably benign |
Het |
Slitrk5 |
A |
G |
14: 111,917,621 (GRCm39) |
Y415C |
probably damaging |
Het |
Sohlh2 |
A |
G |
3: 55,115,043 (GRCm39) |
I343V |
probably benign |
Het |
Sorl1 |
T |
C |
9: 41,890,753 (GRCm39) |
D1922G |
possibly damaging |
Het |
Spats2l |
T |
A |
1: 57,979,623 (GRCm39) |
I243N |
possibly damaging |
Het |
Specc1 |
A |
C |
11: 62,008,701 (GRCm39) |
K152N |
probably damaging |
Het |
Sv2a |
G |
A |
3: 96,101,191 (GRCm39) |
A730T |
possibly damaging |
Het |
Tars2 |
C |
A |
3: 95,654,950 (GRCm39) |
G113C |
probably damaging |
Het |
Tcstv2b |
A |
T |
13: 120,373,836 (GRCm39) |
D151E |
probably benign |
Het |
Tep1 |
T |
C |
14: 51,091,739 (GRCm39) |
K601E |
probably benign |
Het |
Trp53 |
A |
G |
11: 69,480,458 (GRCm39) |
D278G |
probably damaging |
Het |
Ttc39d |
G |
A |
17: 80,524,030 (GRCm39) |
G230R |
probably damaging |
Het |
Tubb2b |
T |
A |
13: 34,312,244 (GRCm39) |
Y183F |
probably damaging |
Het |
Ubxn7 |
T |
A |
16: 32,191,287 (GRCm39) |
C160S |
possibly damaging |
Het |
Vcp |
A |
G |
4: 42,995,894 (GRCm39) |
|
probably null |
Het |
Vmn1r201 |
T |
C |
13: 22,658,995 (GRCm39) |
F70L |
probably benign |
Het |
Vmn1r49 |
C |
T |
6: 90,049,184 (GRCm39) |
V273I |
probably benign |
Het |
Vmn2r103 |
A |
T |
17: 20,014,056 (GRCm39) |
I283L |
probably benign |
Het |
Xpr1 |
T |
C |
1: 155,166,026 (GRCm39) |
T574A |
probably benign |
Het |
Zfp408 |
A |
G |
2: 91,476,363 (GRCm39) |
F364L |
probably damaging |
Het |
Zfyve26 |
A |
G |
12: 79,334,220 (GRCm39) |
L266P |
possibly damaging |
Het |
|
Other mutations in Rev3l |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00332:Rev3l
|
APN |
10 |
39,682,965 (GRCm39) |
missense |
probably benign |
|
IGL00815:Rev3l
|
APN |
10 |
39,735,149 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL00964:Rev3l
|
APN |
10 |
39,740,802 (GRCm39) |
missense |
probably benign |
0.39 |
IGL01765:Rev3l
|
APN |
10 |
39,704,261 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01792:Rev3l
|
APN |
10 |
39,699,336 (GRCm39) |
missense |
probably benign |
|
IGL01950:Rev3l
|
APN |
10 |
39,697,153 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01963:Rev3l
|
APN |
10 |
39,698,733 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02089:Rev3l
|
APN |
10 |
39,701,095 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02288:Rev3l
|
APN |
10 |
39,704,212 (GRCm39) |
missense |
probably benign |
|
IGL02381:Rev3l
|
APN |
10 |
39,697,342 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL02409:Rev3l
|
APN |
10 |
39,697,144 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL02434:Rev3l
|
APN |
10 |
39,698,587 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02570:Rev3l
|
APN |
10 |
39,724,009 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL02581:Rev3l
|
APN |
10 |
39,697,277 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02654:Rev3l
|
APN |
10 |
39,738,730 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02720:Rev3l
|
APN |
10 |
39,698,391 (GRCm39) |
nonsense |
probably null |
|
IGL02746:Rev3l
|
APN |
10 |
39,700,585 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02829:Rev3l
|
APN |
10 |
39,701,236 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02961:Rev3l
|
APN |
10 |
39,703,941 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL02974:Rev3l
|
APN |
10 |
39,738,743 (GRCm39) |
nonsense |
probably null |
|
IGL03029:Rev3l
|
APN |
10 |
39,704,482 (GRCm39) |
missense |
probably benign |
0.34 |
IGL03153:Rev3l
|
APN |
10 |
39,682,874 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03172:Rev3l
|
APN |
10 |
39,700,786 (GRCm39) |
missense |
probably benign |
0.10 |
R0068:Rev3l
|
UTSW |
10 |
39,700,827 (GRCm39) |
missense |
possibly damaging |
0.68 |
R0068:Rev3l
|
UTSW |
10 |
39,700,827 (GRCm39) |
missense |
possibly damaging |
0.68 |
R0153:Rev3l
|
UTSW |
10 |
39,750,124 (GRCm39) |
nonsense |
probably null |
|
R0308:Rev3l
|
UTSW |
10 |
39,700,890 (GRCm39) |
missense |
probably benign |
0.09 |
R0355:Rev3l
|
UTSW |
10 |
39,693,282 (GRCm39) |
missense |
probably damaging |
1.00 |
R0513:Rev3l
|
UTSW |
10 |
39,704,139 (GRCm39) |
missense |
probably benign |
0.00 |
R0523:Rev3l
|
UTSW |
10 |
39,724,045 (GRCm39) |
missense |
probably benign |
0.02 |
R0559:Rev3l
|
UTSW |
10 |
39,700,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R0761:Rev3l
|
UTSW |
10 |
39,750,191 (GRCm39) |
missense |
probably benign |
0.32 |
R1023:Rev3l
|
UTSW |
10 |
39,708,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R1159:Rev3l
|
UTSW |
10 |
39,727,921 (GRCm39) |
nonsense |
probably null |
|
R1398:Rev3l
|
UTSW |
10 |
39,697,579 (GRCm39) |
missense |
probably benign |
0.05 |
R1478:Rev3l
|
UTSW |
10 |
39,659,329 (GRCm39) |
critical splice donor site |
probably null |
|
R1517:Rev3l
|
UTSW |
10 |
39,714,439 (GRCm39) |
missense |
probably benign |
0.34 |
R1527:Rev3l
|
UTSW |
10 |
39,698,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R1635:Rev3l
|
UTSW |
10 |
39,682,658 (GRCm39) |
missense |
probably damaging |
0.98 |
R1695:Rev3l
|
UTSW |
10 |
39,700,612 (GRCm39) |
missense |
probably damaging |
0.97 |
R1695:Rev3l
|
UTSW |
10 |
39,700,611 (GRCm39) |
nonsense |
probably null |
|
R1782:Rev3l
|
UTSW |
10 |
39,675,881 (GRCm39) |
missense |
probably benign |
|
R1815:Rev3l
|
UTSW |
10 |
39,698,867 (GRCm39) |
missense |
probably benign |
0.41 |
R1818:Rev3l
|
UTSW |
10 |
39,704,420 (GRCm39) |
missense |
probably benign |
0.05 |
R2039:Rev3l
|
UTSW |
10 |
39,700,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R2101:Rev3l
|
UTSW |
10 |
39,704,092 (GRCm39) |
missense |
probably benign |
0.00 |
R2141:Rev3l
|
UTSW |
10 |
39,724,045 (GRCm39) |
missense |
probably benign |
0.02 |
R2883:Rev3l
|
UTSW |
10 |
39,701,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R3787:Rev3l
|
UTSW |
10 |
39,722,206 (GRCm39) |
missense |
probably damaging |
0.97 |
R3910:Rev3l
|
UTSW |
10 |
39,696,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R3912:Rev3l
|
UTSW |
10 |
39,696,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R3913:Rev3l
|
UTSW |
10 |
39,696,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R4590:Rev3l
|
UTSW |
10 |
39,682,929 (GRCm39) |
missense |
probably damaging |
1.00 |
R4631:Rev3l
|
UTSW |
10 |
39,704,412 (GRCm39) |
missense |
probably benign |
0.44 |
R4633:Rev3l
|
UTSW |
10 |
39,722,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R4707:Rev3l
|
UTSW |
10 |
39,699,393 (GRCm39) |
missense |
probably damaging |
0.99 |
R4724:Rev3l
|
UTSW |
10 |
39,722,802 (GRCm39) |
nonsense |
probably null |
|
R4810:Rev3l
|
UTSW |
10 |
39,699,721 (GRCm39) |
missense |
probably benign |
0.01 |
R4857:Rev3l
|
UTSW |
10 |
39,714,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R4882:Rev3l
|
UTSW |
10 |
39,697,456 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4928:Rev3l
|
UTSW |
10 |
39,699,981 (GRCm39) |
missense |
probably benign |
0.30 |
R4970:Rev3l
|
UTSW |
10 |
39,699,326 (GRCm39) |
missense |
probably benign |
0.00 |
R4977:Rev3l
|
UTSW |
10 |
39,699,574 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5112:Rev3l
|
UTSW |
10 |
39,699,326 (GRCm39) |
missense |
probably benign |
0.00 |
R5261:Rev3l
|
UTSW |
10 |
39,722,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R5419:Rev3l
|
UTSW |
10 |
39,700,927 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5570:Rev3l
|
UTSW |
10 |
39,728,071 (GRCm39) |
critical splice donor site |
probably null |
|
R5628:Rev3l
|
UTSW |
10 |
39,698,963 (GRCm39) |
missense |
probably damaging |
0.98 |
R5689:Rev3l
|
UTSW |
10 |
39,670,954 (GRCm39) |
missense |
probably damaging |
1.00 |
R5781:Rev3l
|
UTSW |
10 |
39,699,089 (GRCm39) |
missense |
probably benign |
0.00 |
R5829:Rev3l
|
UTSW |
10 |
39,682,902 (GRCm39) |
missense |
probably damaging |
0.97 |
R5984:Rev3l
|
UTSW |
10 |
39,618,685 (GRCm39) |
intron |
probably benign |
|
R5990:Rev3l
|
UTSW |
10 |
39,699,807 (GRCm39) |
missense |
probably benign |
0.17 |
R6054:Rev3l
|
UTSW |
10 |
39,700,146 (GRCm39) |
missense |
probably benign |
0.01 |
R6171:Rev3l
|
UTSW |
10 |
39,738,709 (GRCm39) |
nonsense |
probably null |
|
R6220:Rev3l
|
UTSW |
10 |
39,698,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R6520:Rev3l
|
UTSW |
10 |
39,698,698 (GRCm39) |
missense |
probably benign |
0.06 |
R6798:Rev3l
|
UTSW |
10 |
39,730,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R6811:Rev3l
|
UTSW |
10 |
39,706,917 (GRCm39) |
nonsense |
probably null |
|
R6812:Rev3l
|
UTSW |
10 |
39,699,544 (GRCm39) |
missense |
probably benign |
|
R6904:Rev3l
|
UTSW |
10 |
39,697,477 (GRCm39) |
missense |
probably benign |
|
R6905:Rev3l
|
UTSW |
10 |
39,693,323 (GRCm39) |
missense |
probably benign |
0.18 |
R6938:Rev3l
|
UTSW |
10 |
39,738,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R7037:Rev3l
|
UTSW |
10 |
39,727,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R7124:Rev3l
|
UTSW |
10 |
39,698,163 (GRCm39) |
nonsense |
probably null |
|
R7286:Rev3l
|
UTSW |
10 |
39,699,601 (GRCm39) |
missense |
probably damaging |
0.99 |
R7385:Rev3l
|
UTSW |
10 |
39,699,678 (GRCm39) |
missense |
probably benign |
0.01 |
R7575:Rev3l
|
UTSW |
10 |
39,697,441 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7596:Rev3l
|
UTSW |
10 |
39,697,534 (GRCm39) |
missense |
probably damaging |
1.00 |
R7597:Rev3l
|
UTSW |
10 |
39,698,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R7670:Rev3l
|
UTSW |
10 |
39,712,718 (GRCm39) |
missense |
probably benign |
0.01 |
R7804:Rev3l
|
UTSW |
10 |
39,699,481 (GRCm39) |
missense |
probably benign |
0.34 |
R7818:Rev3l
|
UTSW |
10 |
39,699,898 (GRCm39) |
missense |
possibly damaging |
0.54 |
R7874:Rev3l
|
UTSW |
10 |
39,698,491 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7991:Rev3l
|
UTSW |
10 |
39,739,734 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8059:Rev3l
|
UTSW |
10 |
39,719,491 (GRCm39) |
missense |
probably damaging |
1.00 |
R8174:Rev3l
|
UTSW |
10 |
39,735,111 (GRCm39) |
missense |
probably damaging |
1.00 |
R8187:Rev3l
|
UTSW |
10 |
39,682,693 (GRCm39) |
missense |
probably benign |
|
R8299:Rev3l
|
UTSW |
10 |
39,697,537 (GRCm39) |
missense |
probably benign |
0.01 |
R8352:Rev3l
|
UTSW |
10 |
39,698,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R8452:Rev3l
|
UTSW |
10 |
39,698,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R8468:Rev3l
|
UTSW |
10 |
39,703,987 (GRCm39) |
missense |
probably damaging |
0.99 |
R8487:Rev3l
|
UTSW |
10 |
39,682,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R8512:Rev3l
|
UTSW |
10 |
39,697,534 (GRCm39) |
missense |
probably damaging |
1.00 |
R8554:Rev3l
|
UTSW |
10 |
39,682,838 (GRCm39) |
missense |
probably benign |
0.12 |
R8702:Rev3l
|
UTSW |
10 |
39,714,465 (GRCm39) |
nonsense |
probably null |
|
R8848:Rev3l
|
UTSW |
10 |
39,722,705 (GRCm39) |
missense |
probably damaging |
0.99 |
R8857:Rev3l
|
UTSW |
10 |
39,670,965 (GRCm39) |
nonsense |
probably null |
|
R8870:Rev3l
|
UTSW |
10 |
39,738,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R9094:Rev3l
|
UTSW |
10 |
39,700,809 (GRCm39) |
missense |
probably benign |
|
R9175:Rev3l
|
UTSW |
10 |
39,730,764 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9286:Rev3l
|
UTSW |
10 |
39,682,947 (GRCm39) |
missense |
possibly damaging |
0.54 |
R9299:Rev3l
|
UTSW |
10 |
39,723,999 (GRCm39) |
missense |
probably damaging |
1.00 |
R9307:Rev3l
|
UTSW |
10 |
39,693,149 (GRCm39) |
missense |
probably benign |
0.01 |
R9337:Rev3l
|
UTSW |
10 |
39,698,850 (GRCm39) |
missense |
probably benign |
0.40 |
R9342:Rev3l
|
UTSW |
10 |
39,697,458 (GRCm39) |
missense |
probably benign |
|
R9389:Rev3l
|
UTSW |
10 |
39,698,967 (GRCm39) |
missense |
possibly damaging |
0.47 |
R9395:Rev3l
|
UTSW |
10 |
39,735,219 (GRCm39) |
critical splice donor site |
probably null |
|
R9458:Rev3l
|
UTSW |
10 |
39,659,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R9481:Rev3l
|
UTSW |
10 |
39,701,033 (GRCm39) |
missense |
probably benign |
|
R9646:Rev3l
|
UTSW |
10 |
39,698,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R9686:Rev3l
|
UTSW |
10 |
39,743,384 (GRCm39) |
missense |
possibly damaging |
0.67 |
X0022:Rev3l
|
UTSW |
10 |
39,704,603 (GRCm39) |
critical splice donor site |
probably null |
|
Z1088:Rev3l
|
UTSW |
10 |
39,700,314 (GRCm39) |
missense |
probably benign |
0.41 |
|