Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2210408I21Rik |
A |
T |
13: 77,471,840 (GRCm39) |
N1082Y |
possibly damaging |
Het |
4930444P10Rik |
G |
A |
1: 16,136,451 (GRCm39) |
Q122* |
probably null |
Het |
Afg2a |
A |
G |
3: 37,502,661 (GRCm39) |
N607D |
probably benign |
Het |
Ak8 |
C |
T |
2: 28,625,602 (GRCm39) |
T215M |
probably benign |
Het |
Ano3 |
T |
A |
2: 110,614,074 (GRCm39) |
I210F |
probably benign |
Het |
Atg9b |
A |
G |
5: 24,592,032 (GRCm39) |
F656L |
probably damaging |
Het |
Bscl2 |
T |
C |
19: 8,824,793 (GRCm39) |
M292T |
probably benign |
Het |
Cachd1 |
G |
T |
4: 100,754,978 (GRCm39) |
C143F |
probably damaging |
Het |
Calcoco2 |
GGGCCTTCTCTTTCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTTCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTTCTCCCAGGAGGCCTTCTCTTCC |
GGGCCTTCTCTTTCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTCCTCCCAGGAGGCCTTCTCTTTCTCCCAGGAGGCCTTCTCTTCC |
11: 95,990,808 (GRCm39) |
|
probably benign |
Het |
Ccnb1ip1 |
C |
T |
14: 51,029,450 (GRCm39) |
G204E |
probably benign |
Het |
Ccr1 |
T |
A |
9: 123,764,022 (GRCm39) |
L169F |
probably benign |
Het |
Cdc42bpg |
A |
G |
19: 6,364,550 (GRCm39) |
N593D |
possibly damaging |
Het |
Cdh20 |
T |
C |
1: 104,873,048 (GRCm39) |
S265P |
probably damaging |
Het |
Cenpk |
A |
G |
13: 104,367,365 (GRCm39) |
E67G |
probably damaging |
Het |
Cep76 |
A |
T |
18: 67,773,190 (GRCm39) |
I36K |
probably benign |
Het |
Clock |
A |
T |
5: 76,383,632 (GRCm39) |
I507N |
probably benign |
Het |
Cpne1 |
T |
C |
2: 155,920,873 (GRCm39) |
T110A |
probably benign |
Het |
Crybg2 |
A |
T |
4: 133,818,525 (GRCm39) |
E1427V |
possibly damaging |
Het |
Ctu1 |
A |
C |
7: 43,324,746 (GRCm39) |
K62Q |
probably damaging |
Het |
Dnai4 |
C |
T |
4: 102,944,529 (GRCm39) |
|
probably null |
Het |
Drd5 |
C |
A |
5: 38,477,747 (GRCm39) |
Q247K |
possibly damaging |
Het |
Ect2l |
A |
T |
10: 18,014,608 (GRCm39) |
L808* |
probably null |
Het |
Efcab3 |
A |
G |
11: 104,791,500 (GRCm39) |
T2905A |
probably benign |
Het |
Ficd |
A |
T |
5: 113,876,248 (GRCm39) |
D141V |
probably damaging |
Het |
Fnbp1 |
A |
G |
2: 30,938,222 (GRCm39) |
Y148H |
|
Het |
Gm49368 |
A |
G |
7: 127,700,685 (GRCm39) |
K485R |
probably benign |
Het |
Gpr75 |
C |
A |
11: 30,841,860 (GRCm39) |
A255D |
probably benign |
Het |
Hcrtr2 |
G |
T |
9: 76,153,666 (GRCm39) |
A242D |
probably damaging |
Het |
Iapp |
G |
T |
6: 142,244,602 (GRCm39) |
V10F |
probably benign |
Het |
Ikzf2 |
A |
G |
1: 69,722,417 (GRCm39) |
S31P |
possibly damaging |
Het |
Il18rap |
G |
A |
1: 40,564,280 (GRCm39) |
|
probably benign |
Het |
Irak2 |
A |
T |
6: 113,663,902 (GRCm39) |
N423Y |
probably damaging |
Het |
Itpkb |
A |
G |
1: 180,159,744 (GRCm39) |
|
probably benign |
Het |
Itpr1 |
A |
G |
6: 108,365,172 (GRCm39) |
I874M |
probably damaging |
Het |
Kif26b |
G |
T |
1: 178,692,594 (GRCm39) |
V512F |
probably damaging |
Het |
Lhx6 |
G |
A |
2: 35,995,232 (GRCm39) |
|
probably benign |
Het |
Lrfn1 |
A |
G |
7: 28,158,918 (GRCm39) |
E279G |
possibly damaging |
Het |
Masp1 |
A |
C |
16: 23,314,882 (GRCm39) |
D126E |
probably damaging |
Het |
Mef2a |
T |
C |
7: 66,890,176 (GRCm39) |
I299V |
probably benign |
Het |
Midn |
A |
G |
10: 79,985,939 (GRCm39) |
S10G |
probably damaging |
Het |
Mrps12 |
A |
T |
7: 28,439,361 (GRCm39) |
L118Q |
probably damaging |
Het |
Mxi1 |
G |
A |
19: 53,360,126 (GRCm39) |
G283S |
probably damaging |
Het |
Mzf1 |
A |
G |
7: 12,786,836 (GRCm39) |
V78A |
probably benign |
Het |
Ncoa6 |
A |
G |
2: 155,263,078 (GRCm39) |
V452A |
probably damaging |
Het |
Neb |
A |
G |
2: 52,051,481 (GRCm39) |
Y6600H |
probably damaging |
Het |
Nlgn2 |
A |
G |
11: 69,716,297 (GRCm39) |
L748P |
possibly damaging |
Het |
Nnmt |
A |
T |
9: 48,514,801 (GRCm39) |
L72H |
probably damaging |
Het |
Nrxn3 |
A |
G |
12: 90,171,560 (GRCm39) |
T964A |
probably benign |
Het |
Or12k7 |
A |
G |
2: 36,958,982 (GRCm39) |
I222V |
probably benign |
Het |
Or1e35 |
T |
G |
11: 73,797,725 (GRCm39) |
M198L |
probably benign |
Het |
Or2y16 |
T |
A |
11: 49,335,350 (GRCm39) |
V224E |
probably damaging |
Het |
Or4k35 |
T |
A |
2: 111,100,464 (GRCm39) |
I83F |
possibly damaging |
Het |
Or5h27 |
G |
A |
16: 59,006,130 (GRCm39) |
P239S |
unknown |
Het |
Or8c11 |
A |
G |
9: 38,289,720 (GRCm39) |
N175S |
probably benign |
Het |
Or8g33 |
A |
G |
9: 39,337,548 (GRCm39) |
V273A |
probably damaging |
Het |
Osbpl11 |
A |
G |
16: 33,034,850 (GRCm39) |
N280D |
probably benign |
Het |
Peg10 |
A |
T |
6: 4,754,825 (GRCm39) |
Y202F |
probably damaging |
Het |
Pick1 |
A |
G |
15: 79,140,107 (GRCm39) |
R469G |
unknown |
Het |
Rmc1 |
A |
G |
18: 12,321,618 (GRCm39) |
E473G |
probably benign |
Het |
Rnaseh2b |
T |
A |
14: 62,569,617 (GRCm39) |
L18Q |
probably damaging |
Het |
Rpl19 |
A |
G |
11: 97,920,615 (GRCm39) |
Y122C |
probably benign |
Het |
Selp |
A |
G |
1: 163,964,787 (GRCm39) |
Y483C |
probably damaging |
Het |
Setd2 |
T |
A |
9: 110,423,321 (GRCm39) |
F347L |
|
Het |
Snx14 |
A |
G |
9: 88,295,541 (GRCm39) |
I208T |
probably benign |
Het |
Spag16 |
T |
A |
1: 70,036,017 (GRCm39) |
F348L |
probably benign |
Het |
Spata22 |
A |
T |
11: 73,231,091 (GRCm39) |
N115I |
probably damaging |
Het |
Spata31 |
T |
C |
13: 65,068,818 (GRCm39) |
V322A |
probably benign |
Het |
Stc1 |
A |
T |
14: 69,275,825 (GRCm39) |
H206L |
probably benign |
Het |
Tas2r129 |
A |
G |
6: 132,928,522 (GRCm39) |
D153G |
probably damaging |
Het |
Tmem196 |
T |
A |
12: 119,982,268 (GRCm39) |
N167K |
possibly damaging |
Het |
Tmpo |
T |
C |
10: 90,987,581 (GRCm39) |
T356A |
probably damaging |
Het |
Tnks |
A |
G |
8: 35,314,433 (GRCm39) |
|
probably null |
Het |
Ttbk1 |
A |
C |
17: 46,781,661 (GRCm39) |
L364R |
probably damaging |
Het |
Vmn1r176 |
A |
T |
7: 23,534,480 (GRCm39) |
N224K |
probably damaging |
Het |
Vmn1r36 |
T |
A |
6: 66,693,720 (GRCm39) |
M52L |
probably benign |
Het |
Vmn2r93 |
A |
T |
17: 18,525,320 (GRCm39) |
H326L |
possibly damaging |
Het |
Wrn |
A |
T |
8: 33,819,220 (GRCm39) |
M244K |
probably benign |
Het |
Zcchc24 |
C |
T |
14: 25,757,578 (GRCm39) |
A102T |
probably benign |
Het |
Zfp1010 |
T |
A |
2: 176,957,312 (GRCm39) |
Q62L |
probably benign |
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 |
R2071:Rev3l
|
UTSW |
10 |
39,700,349 (GRCm39) |
missense |
probably benign |
0.17 |
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 |
|
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 |
|