Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933427D14Rik |
T |
C |
11: 72,080,412 (GRCm39) |
E418G |
probably damaging |
Het |
9930012K11Rik |
C |
A |
14: 70,395,071 (GRCm39) |
V28L |
possibly damaging |
Het |
Abtb2 |
C |
T |
2: 103,539,770 (GRCm39) |
R712* |
probably null |
Het |
Acvr1c |
C |
T |
2: 58,177,717 (GRCm39) |
G171S |
probably damaging |
Het |
Ahctf1 |
G |
T |
1: 179,580,853 (GRCm39) |
A1783E |
probably benign |
Het |
Anapc4 |
A |
T |
5: 53,006,170 (GRCm39) |
Q149L |
probably damaging |
Het |
Ankrd27 |
T |
C |
7: 35,327,952 (GRCm39) |
V824A |
possibly damaging |
Het |
Ankrd31 |
G |
C |
13: 96,968,094 (GRCm39) |
C577S |
probably benign |
Het |
Apol7c |
T |
C |
15: 77,410,274 (GRCm39) |
N224S |
probably benign |
Het |
Arl14 |
A |
T |
3: 69,130,029 (GRCm39) |
T59S |
probably benign |
Het |
Astn1 |
T |
A |
1: 158,440,042 (GRCm39) |
I870K |
probably damaging |
Het |
B4galt1 |
A |
T |
4: 40,807,796 (GRCm39) |
V335E |
probably benign |
Het |
C2cd3 |
C |
T |
7: 100,039,448 (GRCm39) |
P216S |
probably benign |
Het |
Cchcr1 |
C |
A |
17: 35,840,015 (GRCm39) |
N711K |
possibly damaging |
Het |
Chd2 |
A |
G |
7: 73,147,558 (GRCm39) |
F467L |
possibly damaging |
Het |
Cntn6 |
A |
T |
6: 104,838,907 (GRCm39) |
E987V |
possibly damaging |
Het |
Col11a2 |
T |
A |
17: 34,272,572 (GRCm39) |
L286H |
probably damaging |
Het |
Cwc22 |
C |
T |
2: 77,759,792 (GRCm39) |
R85Q |
possibly damaging |
Het |
Cyp7a1 |
A |
C |
4: 6,272,587 (GRCm39) |
F209V |
probably damaging |
Het |
Dmtn |
T |
C |
14: 70,852,322 (GRCm39) |
T189A |
possibly damaging |
Het |
Dnhd1 |
C |
G |
7: 105,327,473 (GRCm39) |
N777K |
probably benign |
Het |
Dusp16 |
A |
T |
6: 134,702,842 (GRCm39) |
C216* |
probably null |
Het |
Fan1 |
T |
A |
7: 64,022,234 (GRCm39) |
N340Y |
probably damaging |
Het |
Fbn1 |
T |
C |
2: 125,170,078 (GRCm39) |
N1993S |
probably damaging |
Het |
Fbxw22 |
A |
G |
9: 109,213,030 (GRCm39) |
S306P |
probably benign |
Het |
Ferd3l |
T |
C |
12: 33,978,651 (GRCm39) |
S55P |
probably benign |
Het |
Fpr-rs3 |
A |
G |
17: 20,844,560 (GRCm39) |
S194P |
possibly damaging |
Het |
Gm19965 |
G |
A |
1: 116,748,609 (GRCm39) |
D97N |
probably benign |
Het |
Gtpbp2 |
A |
G |
17: 46,478,914 (GRCm39) |
|
probably benign |
Het |
H3c7 |
G |
T |
13: 23,728,760 (GRCm39) |
V36L |
probably benign |
Het |
Hcn3 |
A |
C |
3: 89,067,152 (GRCm39) |
I72S |
possibly damaging |
Het |
Hk3 |
T |
A |
13: 55,162,278 (GRCm39) |
N109Y |
probably damaging |
Het |
Iqub |
T |
C |
6: 24,505,737 (GRCm39) |
E57G |
possibly damaging |
Het |
Kcnk3 |
T |
A |
5: 30,779,397 (GRCm39) |
M149K |
possibly damaging |
Het |
Kcp |
C |
T |
6: 29,505,719 (GRCm39) |
G51D |
probably benign |
Het |
Kif26a |
C |
A |
12: 112,113,263 (GRCm39) |
A53D |
probably damaging |
Het |
Lifr |
T |
A |
15: 7,202,418 (GRCm39) |
I353K |
probably benign |
Het |
Llph |
A |
T |
10: 120,067,189 (GRCm39) |
N102I |
probably damaging |
Het |
Lmo3 |
C |
A |
6: 138,393,566 (GRCm39) |
R18L |
possibly damaging |
Het |
Lrrc46 |
T |
C |
11: 96,926,371 (GRCm39) |
E175G |
probably benign |
Het |
Ltk |
A |
T |
2: 119,585,075 (GRCm39) |
C128* |
probably null |
Het |
Map1b |
T |
C |
13: 99,571,275 (GRCm39) |
E482G |
probably damaging |
Het |
Mapk8ip2 |
T |
C |
15: 89,344,655 (GRCm39) |
V740A |
probably damaging |
Het |
Miga2 |
T |
C |
2: 30,261,175 (GRCm39) |
W157R |
probably benign |
Het |
Mlip |
A |
G |
9: 77,009,675 (GRCm39) |
*837Q |
probably null |
Het |
Myl1 |
T |
C |
1: 66,984,217 (GRCm39) |
|
probably benign |
Het |
Or1l4 |
T |
C |
2: 37,092,189 (GRCm39) |
L312P |
possibly damaging |
Het |
Or2a5 |
T |
C |
6: 42,873,750 (GRCm39) |
Y122H |
probably benign |
Het |
Or51ab3 |
A |
G |
7: 103,201,075 (GRCm39) |
I28V |
probably benign |
Het |
P3h3 |
A |
T |
6: 124,834,331 (GRCm39) |
V107D |
probably benign |
Het |
Papolb |
A |
T |
5: 142,514,651 (GRCm39) |
S331T |
possibly damaging |
Het |
Pars2 |
T |
G |
4: 106,511,700 (GRCm39) |
V494G |
probably benign |
Het |
Pcdhb3 |
C |
A |
18: 37,434,763 (GRCm39) |
T243K |
probably benign |
Het |
Pde9a |
T |
A |
17: 31,689,698 (GRCm39) |
M415K |
probably damaging |
Het |
Ppp1r9b |
G |
A |
11: 94,882,974 (GRCm39) |
A201T |
probably benign |
Het |
Prl |
A |
G |
13: 27,248,942 (GRCm39) |
N197S |
possibly damaging |
Het |
Prl2c1 |
T |
A |
13: 28,035,724 (GRCm39) |
M32K |
probably benign |
Het |
Prrt4 |
T |
C |
6: 29,170,737 (GRCm39) |
S572G |
possibly damaging |
Het |
Psd |
T |
A |
19: 46,310,858 (GRCm39) |
D397V |
probably damaging |
Het |
Psme2b |
A |
T |
11: 48,836,307 (GRCm39) |
Y213* |
probably null |
Het |
Ptcd3 |
T |
A |
6: 71,874,094 (GRCm39) |
|
probably null |
Het |
Ptprk |
T |
G |
10: 28,210,480 (GRCm39) |
F167L |
probably damaging |
Het |
Rfx7 |
T |
C |
9: 72,524,226 (GRCm39) |
V472A |
probably damaging |
Het |
Sanbr |
A |
G |
11: 23,575,100 (GRCm39) |
L58P |
probably damaging |
Het |
Scnn1g |
T |
C |
7: 121,339,576 (GRCm39) |
L125S |
probably damaging |
Het |
Sec16a |
T |
C |
2: 26,320,124 (GRCm39) |
Y1438C |
probably damaging |
Het |
Serinc3 |
C |
T |
2: 163,476,366 (GRCm39) |
S155N |
probably benign |
Het |
Slc3a2 |
A |
T |
19: 8,690,996 (GRCm39) |
V78E |
probably damaging |
Het |
Slc44a4 |
T |
A |
17: 35,140,044 (GRCm39) |
L23Q |
probably damaging |
Het |
Slco5a1 |
C |
T |
1: 12,951,420 (GRCm39) |
|
probably benign |
Het |
Slit1 |
A |
G |
19: 41,605,154 (GRCm39) |
M899T |
probably benign |
Het |
Sorl1 |
A |
G |
9: 41,933,688 (GRCm39) |
I1094T |
probably benign |
Het |
Spag9 |
T |
A |
11: 93,972,196 (GRCm39) |
L258Q |
probably benign |
Het |
Strip1 |
T |
C |
3: 107,526,252 (GRCm39) |
E488G |
possibly damaging |
Het |
Stx18 |
G |
A |
5: 38,262,235 (GRCm39) |
D30N |
possibly damaging |
Het |
Sync |
T |
C |
4: 129,181,583 (GRCm39) |
|
probably null |
Het |
Syncrip |
A |
G |
9: 88,358,849 (GRCm39) |
V220A |
probably damaging |
Het |
Tagln2 |
T |
C |
1: 172,333,476 (GRCm39) |
I110T |
probably benign |
Het |
Taok1 |
T |
C |
11: 77,432,627 (GRCm39) |
T729A |
probably benign |
Het |
Tgfbrap1 |
C |
T |
1: 43,106,759 (GRCm39) |
V75I |
possibly damaging |
Het |
Tnfrsf21 |
A |
G |
17: 43,327,957 (GRCm39) |
T24A |
probably benign |
Het |
Tnxb |
T |
A |
17: 34,932,131 (GRCm39) |
D2221E |
probably damaging |
Het |
Triml1 |
A |
G |
8: 43,583,603 (GRCm39) |
S333P |
probably damaging |
Het |
Trp53bp1 |
C |
A |
2: 121,029,594 (GRCm39) |
R1862L |
probably damaging |
Het |
Tsc22d1 |
T |
G |
14: 76,655,732 (GRCm39) |
I737S |
possibly damaging |
Het |
U2af2 |
A |
T |
7: 5,082,273 (GRCm39) |
K462N |
possibly damaging |
Het |
Ubap2 |
A |
C |
4: 41,233,631 (GRCm39) |
N86K |
probably damaging |
Het |
Uso1 |
A |
G |
5: 92,343,207 (GRCm39) |
K764E |
probably benign |
Het |
Vmn1r192 |
T |
A |
13: 22,372,122 (GRCm39) |
M33L |
probably benign |
Het |
|
Other mutations in Mroh2a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00990:Mroh2a
|
APN |
1 |
88,172,692 (GRCm39) |
missense |
probably benign |
0.03 |
IGL00990:Mroh2a
|
APN |
1 |
88,161,842 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL00990:Mroh2a
|
APN |
1 |
88,158,468 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03097:Mroh2a
|
UTSW |
1 |
88,163,098 (GRCm39) |
missense |
probably benign |
0.30 |
R0032:Mroh2a
|
UTSW |
1 |
88,183,888 (GRCm39) |
frame shift |
probably null |
|
R0068:Mroh2a
|
UTSW |
1 |
88,183,888 (GRCm39) |
frame shift |
probably null |
|
R0139:Mroh2a
|
UTSW |
1 |
88,185,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R0197:Mroh2a
|
UTSW |
1 |
88,173,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R0242:Mroh2a
|
UTSW |
1 |
88,170,142 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0322:Mroh2a
|
UTSW |
1 |
88,158,402 (GRCm39) |
nonsense |
probably null |
|
R0374:Mroh2a
|
UTSW |
1 |
88,170,142 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0387:Mroh2a
|
UTSW |
1 |
88,173,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R0412:Mroh2a
|
UTSW |
1 |
88,162,938 (GRCm39) |
missense |
probably benign |
0.01 |
R0536:Mroh2a
|
UTSW |
1 |
88,186,386 (GRCm39) |
missense |
probably benign |
0.00 |
R0548:Mroh2a
|
UTSW |
1 |
88,170,142 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0580:Mroh2a
|
UTSW |
1 |
88,171,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R0581:Mroh2a
|
UTSW |
1 |
88,183,888 (GRCm39) |
frame shift |
probably null |
|
R0583:Mroh2a
|
UTSW |
1 |
88,183,888 (GRCm39) |
frame shift |
probably null |
|
R0613:Mroh2a
|
UTSW |
1 |
88,171,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R0652:Mroh2a
|
UTSW |
1 |
88,158,402 (GRCm39) |
nonsense |
probably null |
|
R0657:Mroh2a
|
UTSW |
1 |
88,183,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R0659:Mroh2a
|
UTSW |
1 |
88,170,142 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0659:Mroh2a
|
UTSW |
1 |
88,178,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R0671:Mroh2a
|
UTSW |
1 |
88,170,142 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0675:Mroh2a
|
UTSW |
1 |
88,156,102 (GRCm39) |
missense |
probably damaging |
0.99 |
R0675:Mroh2a
|
UTSW |
1 |
88,178,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R0689:Mroh2a
|
UTSW |
1 |
88,186,386 (GRCm39) |
missense |
probably benign |
0.00 |
R0689:Mroh2a
|
UTSW |
1 |
88,158,402 (GRCm39) |
nonsense |
probably null |
|
R0735:Mroh2a
|
UTSW |
1 |
88,171,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R0761:Mroh2a
|
UTSW |
1 |
88,171,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R0766:Mroh2a
|
UTSW |
1 |
88,158,402 (GRCm39) |
nonsense |
probably null |
|
R0845:Mroh2a
|
UTSW |
1 |
88,186,386 (GRCm39) |
missense |
probably benign |
0.00 |
R0853:Mroh2a
|
UTSW |
1 |
88,186,386 (GRCm39) |
missense |
probably benign |
0.00 |
R0959:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
R0960:Mroh2a
|
UTSW |
1 |
88,170,142 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1004:Mroh2a
|
UTSW |
1 |
88,170,142 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1013:Mroh2a
|
UTSW |
1 |
88,162,334 (GRCm39) |
critical splice donor site |
probably null |
|
R1028:Mroh2a
|
UTSW |
1 |
88,163,098 (GRCm39) |
missense |
probably benign |
0.30 |
R1268:Mroh2a
|
UTSW |
1 |
88,158,402 (GRCm39) |
nonsense |
probably null |
|
R1281:Mroh2a
|
UTSW |
1 |
88,183,889 (GRCm39) |
frame shift |
probably null |
|
R1414:Mroh2a
|
UTSW |
1 |
88,186,386 (GRCm39) |
missense |
probably benign |
0.00 |
R1439:Mroh2a
|
UTSW |
1 |
88,185,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R1441:Mroh2a
|
UTSW |
1 |
88,169,353 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1442:Mroh2a
|
UTSW |
1 |
88,160,075 (GRCm39) |
splice site |
probably benign |
|
R1442:Mroh2a
|
UTSW |
1 |
88,170,142 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1465:Mroh2a
|
UTSW |
1 |
88,185,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R1662:Mroh2a
|
UTSW |
1 |
88,169,340 (GRCm39) |
missense |
probably benign |
0.07 |
R1686:Mroh2a
|
UTSW |
1 |
88,158,402 (GRCm39) |
nonsense |
probably null |
|
R1686:Mroh2a
|
UTSW |
1 |
88,162,334 (GRCm39) |
critical splice donor site |
probably null |
|
R1780:Mroh2a
|
UTSW |
1 |
88,158,402 (GRCm39) |
nonsense |
probably null |
|
R1846:Mroh2a
|
UTSW |
1 |
88,186,386 (GRCm39) |
missense |
probably benign |
0.00 |
R1899:Mroh2a
|
UTSW |
1 |
88,163,098 (GRCm39) |
missense |
probably benign |
0.30 |
R1958:Mroh2a
|
UTSW |
1 |
88,165,213 (GRCm39) |
nonsense |
probably null |
|
R2122:Mroh2a
|
UTSW |
1 |
88,184,476 (GRCm39) |
missense |
probably benign |
0.37 |
R2248:Mroh2a
|
UTSW |
1 |
88,184,476 (GRCm39) |
missense |
probably benign |
0.37 |
R2306:Mroh2a
|
UTSW |
1 |
88,186,386 (GRCm39) |
missense |
probably benign |
0.00 |
R2869:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
R2870:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
R2871:Mroh2a
|
UTSW |
1 |
88,183,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R2872:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
R3408:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
R3608:Mroh2a
|
UTSW |
1 |
88,172,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R3730:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
R3937:Mroh2a
|
UTSW |
1 |
88,186,386 (GRCm39) |
missense |
probably benign |
0.00 |
R4022:Mroh2a
|
UTSW |
1 |
88,173,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R4049:Mroh2a
|
UTSW |
1 |
88,186,386 (GRCm39) |
missense |
probably benign |
0.00 |
R4133:Mroh2a
|
UTSW |
1 |
88,182,687 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4361:Mroh2a
|
UTSW |
1 |
88,182,687 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4392:Mroh2a
|
UTSW |
1 |
88,187,311 (GRCm39) |
missense |
probably damaging |
1.00 |
R4401:Mroh2a
|
UTSW |
1 |
88,182,657 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4402:Mroh2a
|
UTSW |
1 |
88,182,657 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4575:Mroh2a
|
UTSW |
1 |
88,186,386 (GRCm39) |
missense |
probably benign |
0.00 |
R4625:Mroh2a
|
UTSW |
1 |
88,182,687 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4631:Mroh2a
|
UTSW |
1 |
88,186,386 (GRCm39) |
missense |
probably benign |
0.00 |
R4665:Mroh2a
|
UTSW |
1 |
88,169,340 (GRCm39) |
missense |
probably benign |
0.07 |
R4701:Mroh2a
|
UTSW |
1 |
88,162,334 (GRCm39) |
critical splice donor site |
probably null |
|
R4701:Mroh2a
|
UTSW |
1 |
88,169,340 (GRCm39) |
missense |
probably benign |
0.07 |
R4771:Mroh2a
|
UTSW |
1 |
88,179,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R4795:Mroh2a
|
UTSW |
1 |
88,186,386 (GRCm39) |
missense |
probably benign |
0.00 |
R4839:Mroh2a
|
UTSW |
1 |
88,165,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R4873:Mroh2a
|
UTSW |
1 |
88,182,657 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4875:Mroh2a
|
UTSW |
1 |
88,182,657 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4896:Mroh2a
|
UTSW |
1 |
88,184,476 (GRCm39) |
missense |
probably benign |
0.37 |
R5007:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
R5031:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
R5062:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
R5301:Mroh2a
|
UTSW |
1 |
88,186,386 (GRCm39) |
missense |
probably benign |
0.00 |
R5367:Mroh2a
|
UTSW |
1 |
88,182,687 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5371:Mroh2a
|
UTSW |
1 |
88,186,386 (GRCm39) |
missense |
probably benign |
0.00 |
R5446:Mroh2a
|
UTSW |
1 |
88,182,687 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5484:Mroh2a
|
UTSW |
1 |
88,186,386 (GRCm39) |
missense |
probably benign |
0.00 |
R5506:Mroh2a
|
UTSW |
1 |
88,186,386 (GRCm39) |
missense |
probably benign |
0.00 |
R5561:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
R5615:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
R5825:Mroh2a
|
UTSW |
1 |
88,158,402 (GRCm39) |
nonsense |
probably null |
|
R5891:Mroh2a
|
UTSW |
1 |
88,169,337 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5906:Mroh2a
|
UTSW |
1 |
88,186,386 (GRCm39) |
missense |
probably benign |
0.00 |
R5928:Mroh2a
|
UTSW |
1 |
88,169,340 (GRCm39) |
missense |
probably benign |
0.07 |
R6004:Mroh2a
|
UTSW |
1 |
88,176,377 (GRCm39) |
missense |
probably damaging |
1.00 |
R6035:Mroh2a
|
UTSW |
1 |
88,158,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R6064:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
R6074:Mroh2a
|
UTSW |
1 |
88,186,386 (GRCm39) |
missense |
probably benign |
0.00 |
R6091:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
R6127:Mroh2a
|
UTSW |
1 |
88,162,334 (GRCm39) |
critical splice donor site |
probably null |
|
R6234:Mroh2a
|
UTSW |
1 |
88,184,476 (GRCm39) |
missense |
probably benign |
0.37 |
R6234:Mroh2a
|
UTSW |
1 |
88,162,334 (GRCm39) |
critical splice donor site |
probably null |
|
R6244:Mroh2a
|
UTSW |
1 |
88,184,476 (GRCm39) |
missense |
probably benign |
0.37 |
R6464:Mroh2a
|
UTSW |
1 |
88,185,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R6465:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
R6575:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
R6809:Mroh2a
|
UTSW |
1 |
88,162,938 (GRCm39) |
missense |
probably benign |
0.01 |
R6819:Mroh2a
|
UTSW |
1 |
88,170,142 (GRCm39) |
missense |
possibly damaging |
0.77 |
R6854:Mroh2a
|
UTSW |
1 |
88,171,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R7126:Mroh2a
|
UTSW |
1 |
88,182,657 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7818:Mroh2a
|
UTSW |
1 |
88,162,334 (GRCm39) |
critical splice donor site |
probably null |
|
R8350:Mroh2a
|
UTSW |
1 |
88,171,805 (GRCm39) |
splice site |
probably null |
|
R9414:Mroh2a
|
UTSW |
1 |
88,179,096 (GRCm39) |
missense |
probably benign |
0.26 |
RF024:Mroh2a
|
UTSW |
1 |
88,170,207 (GRCm39) |
missense |
probably damaging |
1.00 |
V5622:Mroh2a
|
UTSW |
1 |
88,154,813 (GRCm39) |
start gained |
probably benign |
|
V8831:Mroh2a
|
UTSW |
1 |
88,183,889 (GRCm39) |
frame shift |
probably null |
|
X0027:Mroh2a
|
UTSW |
1 |
88,176,335 (GRCm39) |
missense |
possibly damaging |
0.86 |
X0028:Mroh2a
|
UTSW |
1 |
88,183,888 (GRCm39) |
frame shift |
probably null |
|
X0028:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
X0033:Mroh2a
|
UTSW |
1 |
88,183,888 (GRCm39) |
frame shift |
probably null |
|
X0034:Mroh2a
|
UTSW |
1 |
88,183,888 (GRCm39) |
frame shift |
probably null |
|
X0034:Mroh2a
|
UTSW |
1 |
88,160,014 (GRCm39) |
missense |
probably damaging |
1.00 |
X0034:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
X0039:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
X0057:Mroh2a
|
UTSW |
1 |
88,183,888 (GRCm39) |
frame shift |
probably null |
|
X0057:Mroh2a
|
UTSW |
1 |
88,183,377 (GRCm39) |
missense |
probably benign |
0.25 |
X0057:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
X0063:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
Z1188:Mroh2a
|
UTSW |
1 |
88,162,938 (GRCm39) |
missense |
probably benign |
0.01 |
Z1190:Mroh2a
|
UTSW |
1 |
88,159,979 (GRCm39) |
frame shift |
probably null |
|
Z1192:Mroh2a
|
UTSW |
1 |
88,162,938 (GRCm39) |
missense |
probably benign |
0.01 |
|