Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610008E11Rik |
T |
C |
10: 78,903,833 (GRCm39) |
Y133C |
probably benign |
Het |
Adcy5 |
G |
A |
16: 35,091,195 (GRCm39) |
|
probably benign |
Het |
Asb17 |
A |
G |
3: 153,550,052 (GRCm39) |
K28R |
probably damaging |
Het |
Bbs10 |
G |
T |
10: 111,135,244 (GRCm39) |
C119F |
probably damaging |
Het |
Camk2g |
G |
A |
14: 20,816,280 (GRCm39) |
Q119* |
probably null |
Het |
Cdh18 |
A |
T |
15: 23,226,838 (GRCm39) |
I46L |
possibly damaging |
Het |
Cimip2a |
T |
C |
2: 25,110,135 (GRCm39) |
|
probably benign |
Het |
Clmn |
T |
A |
12: 104,747,817 (GRCm39) |
N577Y |
probably damaging |
Het |
Col1a2 |
G |
A |
6: 4,518,822 (GRCm39) |
|
probably benign |
Het |
Crocc |
T |
C |
4: 140,774,387 (GRCm39) |
E63G |
probably benign |
Het |
Crocc |
T |
C |
4: 140,757,087 (GRCm39) |
T965A |
probably benign |
Het |
Cryzl2 |
A |
G |
1: 157,293,294 (GRCm39) |
I132V |
probably benign |
Het |
Csgalnact2 |
T |
C |
6: 118,103,073 (GRCm39) |
|
probably benign |
Het |
Ctr9 |
T |
C |
7: 110,645,479 (GRCm39) |
S569P |
probably damaging |
Het |
Cul3 |
A |
G |
1: 80,255,203 (GRCm39) |
|
probably benign |
Het |
Dcp2 |
G |
A |
18: 44,543,300 (GRCm39) |
S286N |
probably benign |
Het |
Dgkz |
C |
T |
2: 91,775,696 (GRCm39) |
R189H |
probably benign |
Het |
Dst |
A |
G |
1: 34,221,848 (GRCm39) |
T2551A |
probably benign |
Het |
Kcna4 |
T |
A |
2: 107,126,417 (GRCm39) |
S384T |
probably benign |
Het |
Klhl17 |
T |
C |
4: 156,317,204 (GRCm39) |
|
probably null |
Het |
Kmt2e |
C |
A |
5: 23,708,032 (GRCm39) |
S1865* |
probably null |
Het |
L3mbtl1 |
G |
A |
2: 162,807,967 (GRCm39) |
R534H |
probably damaging |
Het |
Lmnb2 |
A |
T |
10: 80,742,088 (GRCm39) |
M1K |
probably null |
Het |
Lrp1b |
T |
C |
2: 41,075,947 (GRCm39) |
D1784G |
probably damaging |
Het |
Lrrc34 |
A |
G |
3: 30,685,425 (GRCm39) |
|
probably null |
Het |
Megf10 |
C |
A |
18: 57,421,048 (GRCm39) |
Y895* |
probably null |
Het |
Mesd |
G |
T |
7: 83,544,951 (GRCm39) |
A143S |
probably damaging |
Het |
Mfap3l |
G |
T |
8: 61,124,615 (GRCm39) |
V286L |
possibly damaging |
Het |
Mroh2a |
G |
A |
1: 88,171,672 (GRCm39) |
R770Q |
probably damaging |
Het |
Nek1 |
T |
A |
8: 61,542,489 (GRCm39) |
D717E |
probably benign |
Het |
Nudt12 |
A |
T |
17: 59,318,064 (GRCm39) |
D60E |
probably benign |
Het |
Nup205 |
C |
T |
6: 35,173,363 (GRCm39) |
|
probably benign |
Het |
Or11g27 |
T |
C |
14: 50,771,159 (GRCm39) |
S97P |
possibly damaging |
Het |
Or2j3 |
A |
T |
17: 38,616,282 (GRCm39) |
H23Q |
probably benign |
Het |
Or4a75 |
T |
C |
2: 89,448,179 (GRCm39) |
D119G |
probably damaging |
Het |
Or5w19 |
C |
T |
2: 87,698,880 (GRCm39) |
P182S |
possibly damaging |
Het |
Pacs2 |
T |
A |
12: 113,023,688 (GRCm39) |
|
probably benign |
Het |
Pcdha9 |
T |
A |
18: 37,133,016 (GRCm39) |
L695* |
probably null |
Het |
Pira12 |
A |
T |
7: 3,896,978 (GRCm39) |
|
probably null |
Het |
Pkd1l1 |
A |
G |
11: 8,804,375 (GRCm39) |
S1739P |
probably damaging |
Het |
Polr1e |
C |
A |
4: 45,027,392 (GRCm39) |
D207E |
probably damaging |
Het |
Polr3f |
T |
A |
2: 144,376,327 (GRCm39) |
V142E |
probably damaging |
Het |
Psma6 |
T |
A |
12: 55,459,127 (GRCm39) |
W170R |
possibly damaging |
Het |
Rps6ka5 |
C |
T |
12: 100,537,141 (GRCm39) |
A530T |
probably damaging |
Het |
Simc1 |
T |
C |
13: 54,674,387 (GRCm39) |
Y912H |
probably damaging |
Het |
Tnfrsf1b |
T |
C |
4: 144,942,670 (GRCm39) |
D371G |
possibly damaging |
Het |
Trank1 |
T |
C |
9: 111,195,681 (GRCm39) |
V1235A |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,577,102 (GRCm39) |
E24597G |
probably damaging |
Het |
Ubr2 |
G |
A |
17: 47,294,242 (GRCm39) |
P297L |
probably damaging |
Het |
Unc5d |
A |
T |
8: 29,186,560 (GRCm39) |
|
probably null |
Het |
Xpo4 |
A |
G |
14: 57,850,840 (GRCm39) |
F355L |
probably 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 |
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 |
|
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 |
|