Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc6 |
A |
G |
7: 45,644,661 (GRCm39) |
L838P |
probably damaging |
Het |
Adam34l |
T |
G |
8: 44,078,281 (GRCm39) |
N648H |
probably damaging |
Het |
Adgrl4 |
T |
A |
3: 151,248,895 (GRCm39) |
F728I |
probably damaging |
Het |
Asap1 |
A |
G |
15: 64,184,304 (GRCm39) |
V7A |
probably benign |
Het |
B230104I21Rik |
A |
G |
4: 154,434,050 (GRCm39) |
|
probably benign |
Het |
C4b |
A |
T |
17: 34,958,649 (GRCm39) |
S562T |
probably benign |
Het |
Carmil2 |
A |
G |
8: 106,422,121 (GRCm39) |
Y1130C |
probably damaging |
Het |
Cit |
A |
T |
5: 116,024,740 (GRCm39) |
K328* |
probably null |
Het |
Col18a1 |
T |
C |
10: 76,949,137 (GRCm39) |
D125G |
unknown |
Het |
Cxadr |
T |
C |
16: 78,125,996 (GRCm39) |
V122A |
probably damaging |
Het |
Cyp2d22 |
G |
A |
15: 82,260,053 (GRCm39) |
P44S |
probably damaging |
Het |
Elapor1 |
A |
G |
3: 108,378,745 (GRCm39) |
V351A |
possibly damaging |
Het |
Gabrr1 |
A |
G |
4: 33,148,964 (GRCm39) |
T74A |
probably benign |
Het |
Gfm2 |
C |
A |
13: 97,309,086 (GRCm39) |
A597E |
probably benign |
Het |
H2-T22 |
T |
C |
17: 36,351,408 (GRCm39) |
Y274C |
probably damaging |
Het |
Has2 |
C |
A |
15: 56,531,817 (GRCm39) |
W299C |
probably damaging |
Het |
Hsd17b6 |
A |
G |
10: 127,827,227 (GRCm39) |
S282P |
probably benign |
Het |
Itga1 |
T |
C |
13: 115,110,676 (GRCm39) |
I972V |
probably benign |
Het |
Itih5 |
T |
A |
2: 10,254,187 (GRCm39) |
Y813N |
probably damaging |
Het |
Kctd16 |
A |
G |
18: 40,663,848 (GRCm39) |
T326A |
possibly damaging |
Het |
Klhdc1 |
T |
C |
12: 69,316,642 (GRCm39) |
S342P |
probably damaging |
Het |
Kmt2a |
T |
C |
9: 44,742,650 (GRCm39) |
I1682M |
unknown |
Het |
Lamc1 |
T |
C |
1: 153,116,200 (GRCm39) |
K994E |
possibly damaging |
Het |
Lig1 |
T |
G |
7: 13,030,270 (GRCm39) |
S416A |
probably benign |
Het |
Lims1 |
A |
G |
10: 58,248,263 (GRCm39) |
E240G |
probably damaging |
Het |
Lnpk |
T |
C |
2: 74,399,316 (GRCm39) |
M76V |
probably benign |
Het |
Lrrtm4 |
T |
A |
6: 79,999,428 (GRCm39) |
L280* |
probably null |
Het |
Mfap3l |
A |
T |
8: 61,124,315 (GRCm39) |
I186F |
possibly damaging |
Het |
Mta3 |
T |
C |
17: 84,083,011 (GRCm39) |
F234L |
probably benign |
Het |
Muc4 |
C |
G |
16: 32,575,221 (GRCm39) |
Q1269E |
probably benign |
Het |
Mybpc2 |
C |
T |
7: 44,159,223 (GRCm39) |
G609D |
probably damaging |
Het |
Naga |
A |
T |
15: 82,219,035 (GRCm39) |
D237E |
probably benign |
Het |
Naip6 |
C |
T |
13: 100,437,108 (GRCm39) |
A472T |
probably benign |
Het |
Nbn |
G |
A |
4: 15,963,911 (GRCm39) |
S104N |
probably damaging |
Het |
Nipsnap2 |
T |
C |
5: 129,816,637 (GRCm39) |
L60P |
probably damaging |
Het |
Or4f47 |
T |
A |
2: 111,972,925 (GRCm39) |
F212I |
probably benign |
Het |
Or8b1b |
G |
A |
9: 38,375,802 (GRCm39) |
G155D |
probably benign |
Het |
Pclo |
C |
T |
5: 14,727,601 (GRCm39) |
T2153I |
unknown |
Het |
Pclo |
A |
C |
5: 14,908,869 (GRCm39) |
K5059T |
unknown |
Het |
Pdlim2 |
C |
A |
14: 70,403,645 (GRCm39) |
A256S |
possibly damaging |
Het |
Pira2 |
T |
C |
7: 3,845,460 (GRCm39) |
D308G |
probably damaging |
Het |
Proc |
G |
T |
18: 32,256,689 (GRCm39) |
A326E |
probably damaging |
Het |
Rab40b |
T |
C |
11: 121,248,709 (GRCm39) |
D182G |
probably benign |
Het |
Rai14 |
A |
G |
15: 10,574,937 (GRCm39) |
S703P |
possibly damaging |
Het |
Rdx |
C |
T |
9: 51,972,196 (GRCm39) |
P2L |
possibly damaging |
Het |
Recql5 |
T |
C |
11: 115,819,207 (GRCm39) |
K120E |
probably benign |
Het |
Slc2a6 |
G |
T |
2: 26,917,195 (GRCm39) |
D70E |
possibly damaging |
Het |
Slc6a17 |
A |
T |
3: 107,378,668 (GRCm39) |
D671E |
possibly damaging |
Het |
Slc7a8 |
G |
A |
14: 55,018,857 (GRCm39) |
|
probably benign |
Het |
Srpk2 |
A |
G |
5: 23,753,517 (GRCm39) |
Y79H |
possibly damaging |
Het |
Traf3ip1 |
T |
A |
1: 91,439,167 (GRCm39) |
I361K |
probably damaging |
Het |
Trpm8 |
A |
G |
1: 88,255,918 (GRCm39) |
Y191C |
probably damaging |
Het |
Ubr3 |
T |
C |
2: 69,803,812 (GRCm39) |
V1135A |
possibly damaging |
Het |
Usp12 |
C |
A |
5: 146,691,179 (GRCm39) |
|
probably null |
Het |
Vmn1r44 |
C |
A |
6: 89,870,818 (GRCm39) |
P188Q |
probably benign |
Het |
Xirp2 |
T |
A |
2: 67,356,099 (GRCm39) |
V3620D |
possibly damaging |
Het |
Zcchc14 |
A |
T |
8: 122,335,239 (GRCm39) |
S294T |
unknown |
Het |
Zfp800 |
T |
C |
6: 28,260,764 (GRCm39) |
D5G |
probably damaging |
Het |
Zfp87 |
C |
T |
13: 67,665,412 (GRCm39) |
R350Q |
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 |
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 |
|