Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acod1 |
C |
T |
14: 103,292,781 (GRCm39) |
T435M |
probably benign |
Het |
Adgrf5 |
T |
C |
17: 43,763,331 (GRCm39) |
F1078L |
probably benign |
Het |
Adh6a |
A |
T |
3: 138,030,708 (GRCm39) |
N110I |
probably damaging |
Het |
Aldh16a1 |
T |
C |
7: 44,798,212 (GRCm39) |
|
probably benign |
Het |
Aopep |
G |
A |
13: 63,446,565 (GRCm39) |
E123K |
probably damaging |
Het |
Arhgef17 |
A |
G |
7: 100,531,692 (GRCm39) |
F1302S |
probably damaging |
Het |
Bcl2a1a |
C |
T |
9: 88,839,506 (GRCm39) |
R135W |
probably damaging |
Het |
Bpifa6 |
T |
C |
2: 153,824,908 (GRCm39) |
S28P |
possibly damaging |
Het |
C9 |
A |
G |
15: 6,520,944 (GRCm39) |
D51G |
probably damaging |
Het |
Cfb |
T |
A |
17: 35,078,044 (GRCm39) |
H962L |
probably benign |
Het |
Chn2 |
G |
A |
6: 54,267,388 (GRCm39) |
M292I |
probably damaging |
Het |
Clec16a |
T |
A |
16: 10,462,747 (GRCm39) |
|
probably null |
Het |
Cyp1a1 |
T |
C |
9: 57,609,039 (GRCm39) |
S307P |
probably benign |
Het |
Dsg3 |
T |
C |
18: 20,664,616 (GRCm39) |
V538A |
probably benign |
Het |
Erbb3 |
G |
A |
10: 128,408,639 (GRCm39) |
Q815* |
probably null |
Het |
Fam90a1a |
C |
A |
8: 22,453,862 (GRCm39) |
Q406K |
possibly damaging |
Het |
Frmd3 |
T |
C |
4: 74,106,109 (GRCm39) |
V585A |
probably benign |
Het |
Gm8214 |
T |
C |
1: 183,414,094 (GRCm39) |
|
noncoding transcript |
Het |
Gpld1 |
G |
A |
13: 25,168,799 (GRCm39) |
G771D |
probably damaging |
Het |
Gpr20 |
T |
C |
15: 73,567,585 (GRCm39) |
N268S |
probably benign |
Het |
Gria2 |
A |
T |
3: 80,614,204 (GRCm39) |
I612N |
probably damaging |
Het |
Ifit1bl1 |
T |
C |
19: 34,572,010 (GRCm39) |
E149G |
probably damaging |
Het |
Ighv1-82 |
T |
C |
12: 115,916,280 (GRCm39) |
T77A |
probably benign |
Het |
Ighv2-9 |
G |
T |
12: 113,842,839 (GRCm39) |
T76K |
probably damaging |
Het |
Igkv6-13 |
A |
T |
6: 70,435,019 (GRCm39) |
M1K |
probably null |
Het |
Igkv8-21 |
A |
T |
6: 70,292,141 (GRCm39) |
S34T |
probably benign |
Het |
Itpr1 |
A |
G |
6: 108,458,184 (GRCm39) |
N1985D |
probably damaging |
Het |
Jkampl |
A |
G |
6: 73,446,252 (GRCm39) |
V99A |
probably benign |
Het |
Lama3 |
T |
C |
18: 12,637,454 (GRCm39) |
|
probably null |
Het |
Lamc2 |
T |
C |
1: 153,041,915 (GRCm39) |
Y73C |
probably damaging |
Het |
Maff |
A |
G |
15: 79,241,898 (GRCm39) |
D105G |
probably damaging |
Het |
Mep1a |
C |
T |
17: 43,797,132 (GRCm39) |
V312M |
possibly damaging |
Het |
Mfap4 |
C |
A |
11: 61,376,335 (GRCm39) |
|
probably benign |
Het |
Mplkipl1 |
C |
T |
19: 61,164,364 (GRCm39) |
G24R |
unknown |
Het |
Mrgbp |
A |
T |
2: 180,227,107 (GRCm39) |
|
silent |
Het |
Mtmr4 |
T |
C |
11: 87,501,761 (GRCm39) |
L548S |
probably damaging |
Het |
Myo9a |
T |
C |
9: 59,728,932 (GRCm39) |
I596T |
probably damaging |
Het |
Or2f1b |
G |
T |
6: 42,739,352 (GRCm39) |
R122L |
probably benign |
Het |
Or52e3 |
C |
T |
7: 102,869,629 (GRCm39) |
R235* |
probably null |
Het |
Pcsk5 |
T |
G |
19: 17,538,114 (GRCm39) |
Q904H |
probably benign |
Het |
Pdzrn3 |
G |
T |
6: 101,128,970 (GRCm39) |
H565Q |
probably damaging |
Het |
Phkg2 |
C |
T |
7: 127,176,792 (GRCm39) |
R61W |
probably damaging |
Het |
Pkd2l1 |
C |
A |
19: 44,142,573 (GRCm39) |
A490S |
probably damaging |
Het |
Pomgnt1 |
T |
A |
4: 116,012,087 (GRCm39) |
I337N |
probably damaging |
Het |
Psmd3 |
T |
C |
11: 98,573,752 (GRCm39) |
V66A |
probably benign |
Het |
Ptger3 |
T |
C |
3: 157,272,931 (GRCm39) |
S93P |
probably damaging |
Het |
Rbm27 |
T |
A |
18: 42,434,840 (GRCm39) |
D301E |
probably damaging |
Het |
Rdh16 |
A |
T |
10: 127,637,382 (GRCm39) |
|
probably null |
Het |
Slc35a5 |
A |
T |
16: 44,964,655 (GRCm39) |
F193I |
probably benign |
Het |
Slc4a4 |
A |
G |
5: 89,186,420 (GRCm39) |
K167R |
probably damaging |
Het |
Sort1 |
A |
T |
3: 108,262,857 (GRCm39) |
T772S |
possibly damaging |
Het |
Sptbn5 |
T |
A |
2: 119,879,238 (GRCm39) |
|
noncoding transcript |
Het |
Stard5 |
G |
T |
7: 83,282,489 (GRCm39) |
|
probably benign |
Het |
Tbc1d22a |
A |
G |
15: 86,119,886 (GRCm39) |
T61A |
probably damaging |
Het |
Tox2 |
T |
C |
2: 163,162,567 (GRCm39) |
L479P |
probably damaging |
Het |
Usp53 |
A |
T |
3: 122,752,769 (GRCm39) |
M80K |
probably damaging |
Het |
Vmn1r209 |
A |
T |
13: 22,990,135 (GRCm39) |
L185Q |
probably damaging |
Het |
Vmn2r59 |
A |
G |
7: 41,661,862 (GRCm39) |
I651T |
probably benign |
Het |
Vsig1 |
G |
T |
X: 139,827,135 (GRCm39) |
A95S |
probably benign |
Het |
Zfhx4 |
T |
C |
3: 5,478,127 (GRCm39) |
S3556P |
possibly damaging |
Het |
|
Other mutations in Myo7b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00391:Myo7b
|
APN |
18 |
32,154,609 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL01799:Myo7b
|
APN |
18 |
32,095,823 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01881:Myo7b
|
APN |
18 |
32,133,320 (GRCm39) |
splice site |
probably benign |
|
IGL01883:Myo7b
|
APN |
18 |
32,131,204 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01934:Myo7b
|
APN |
18 |
32,134,394 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01980:Myo7b
|
APN |
18 |
32,094,953 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02506:Myo7b
|
APN |
18 |
32,100,207 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02704:Myo7b
|
APN |
18 |
32,100,014 (GRCm39) |
missense |
probably benign |
0.13 |
IGL02929:Myo7b
|
APN |
18 |
32,127,978 (GRCm39) |
missense |
probably benign |
0.19 |
IGL03149:Myo7b
|
APN |
18 |
32,147,355 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03335:Myo7b
|
APN |
18 |
32,118,073 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL03372:Myo7b
|
APN |
18 |
32,131,654 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03385:Myo7b
|
APN |
18 |
32,122,630 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4131001:Myo7b
|
UTSW |
18 |
32,094,259 (GRCm39) |
missense |
probably benign |
0.17 |
PIT4445001:Myo7b
|
UTSW |
18 |
32,095,405 (GRCm39) |
missense |
probably damaging |
0.96 |
PIT4445001:Myo7b
|
UTSW |
18 |
32,092,519 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0034:Myo7b
|
UTSW |
18 |
32,093,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R0138:Myo7b
|
UTSW |
18 |
32,143,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R0149:Myo7b
|
UTSW |
18 |
32,147,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R0226:Myo7b
|
UTSW |
18 |
32,105,949 (GRCm39) |
missense |
probably benign |
0.00 |
R0312:Myo7b
|
UTSW |
18 |
32,147,390 (GRCm39) |
missense |
possibly damaging |
0.68 |
R0361:Myo7b
|
UTSW |
18 |
32,147,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R0506:Myo7b
|
UTSW |
18 |
32,097,439 (GRCm39) |
critical splice donor site |
probably null |
|
R0524:Myo7b
|
UTSW |
18 |
32,146,477 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0645:Myo7b
|
UTSW |
18 |
32,127,962 (GRCm39) |
missense |
probably benign |
0.10 |
R0724:Myo7b
|
UTSW |
18 |
32,138,602 (GRCm39) |
splice site |
probably benign |
|
R0731:Myo7b
|
UTSW |
18 |
32,094,878 (GRCm39) |
splice site |
probably null |
|
R0762:Myo7b
|
UTSW |
18 |
32,116,997 (GRCm39) |
missense |
probably benign |
0.01 |
R0843:Myo7b
|
UTSW |
18 |
32,107,137 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0894:Myo7b
|
UTSW |
18 |
32,133,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R0966:Myo7b
|
UTSW |
18 |
32,131,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R1205:Myo7b
|
UTSW |
18 |
32,127,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R1387:Myo7b
|
UTSW |
18 |
32,116,805 (GRCm39) |
splice site |
probably benign |
|
R1523:Myo7b
|
UTSW |
18 |
32,099,929 (GRCm39) |
missense |
probably damaging |
1.00 |
R1544:Myo7b
|
UTSW |
18 |
32,127,962 (GRCm39) |
missense |
probably benign |
0.10 |
R1623:Myo7b
|
UTSW |
18 |
32,133,104 (GRCm39) |
missense |
probably damaging |
1.00 |
R1780:Myo7b
|
UTSW |
18 |
32,094,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R1785:Myo7b
|
UTSW |
18 |
32,127,950 (GRCm39) |
missense |
probably benign |
|
R1786:Myo7b
|
UTSW |
18 |
32,127,950 (GRCm39) |
missense |
probably benign |
|
R1796:Myo7b
|
UTSW |
18 |
32,119,728 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1907:Myo7b
|
UTSW |
18 |
32,110,052 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2027:Myo7b
|
UTSW |
18 |
32,118,013 (GRCm39) |
missense |
probably benign |
|
R2102:Myo7b
|
UTSW |
18 |
32,133,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R2174:Myo7b
|
UTSW |
18 |
32,116,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R2272:Myo7b
|
UTSW |
18 |
32,110,096 (GRCm39) |
missense |
probably benign |
0.41 |
R2323:Myo7b
|
UTSW |
18 |
32,104,398 (GRCm39) |
missense |
probably damaging |
1.00 |
R2365:Myo7b
|
UTSW |
18 |
32,147,384 (GRCm39) |
missense |
probably damaging |
0.98 |
R3078:Myo7b
|
UTSW |
18 |
32,100,237 (GRCm39) |
missense |
probably benign |
0.04 |
R3522:Myo7b
|
UTSW |
18 |
32,143,132 (GRCm39) |
missense |
probably damaging |
1.00 |
R3788:Myo7b
|
UTSW |
18 |
32,107,165 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3880:Myo7b
|
UTSW |
18 |
32,102,567 (GRCm39) |
missense |
probably damaging |
0.96 |
R4334:Myo7b
|
UTSW |
18 |
32,110,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R4343:Myo7b
|
UTSW |
18 |
32,116,680 (GRCm39) |
missense |
probably damaging |
1.00 |
R4497:Myo7b
|
UTSW |
18 |
32,147,282 (GRCm39) |
missense |
probably benign |
0.06 |
R4498:Myo7b
|
UTSW |
18 |
32,147,282 (GRCm39) |
missense |
probably benign |
0.06 |
R4551:Myo7b
|
UTSW |
18 |
32,118,161 (GRCm39) |
missense |
probably benign |
0.01 |
R4593:Myo7b
|
UTSW |
18 |
32,146,428 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4646:Myo7b
|
UTSW |
18 |
32,127,422 (GRCm39) |
missense |
probably benign |
0.25 |
R4648:Myo7b
|
UTSW |
18 |
32,100,178 (GRCm39) |
splice site |
probably null |
|
R4737:Myo7b
|
UTSW |
18 |
32,131,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R4765:Myo7b
|
UTSW |
18 |
32,094,953 (GRCm39) |
missense |
probably benign |
0.00 |
R4790:Myo7b
|
UTSW |
18 |
32,133,158 (GRCm39) |
splice site |
probably null |
|
R4909:Myo7b
|
UTSW |
18 |
32,097,489 (GRCm39) |
missense |
probably benign |
0.01 |
R5027:Myo7b
|
UTSW |
18 |
32,108,265 (GRCm39) |
missense |
probably benign |
0.22 |
R5034:Myo7b
|
UTSW |
18 |
32,104,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R5112:Myo7b
|
UTSW |
18 |
32,116,640 (GRCm39) |
missense |
probably damaging |
1.00 |
R5266:Myo7b
|
UTSW |
18 |
32,131,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R5267:Myo7b
|
UTSW |
18 |
32,131,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R5348:Myo7b
|
UTSW |
18 |
32,116,972 (GRCm39) |
missense |
probably damaging |
0.96 |
R5457:Myo7b
|
UTSW |
18 |
32,104,503 (GRCm39) |
splice site |
probably null |
|
R5540:Myo7b
|
UTSW |
18 |
32,140,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R5628:Myo7b
|
UTSW |
18 |
32,107,240 (GRCm39) |
missense |
probably benign |
|
R5815:Myo7b
|
UTSW |
18 |
32,099,341 (GRCm39) |
missense |
probably damaging |
1.00 |
R6062:Myo7b
|
UTSW |
18 |
32,101,043 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6137:Myo7b
|
UTSW |
18 |
32,133,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R6158:Myo7b
|
UTSW |
18 |
32,121,602 (GRCm39) |
missense |
probably benign |
0.00 |
R6218:Myo7b
|
UTSW |
18 |
32,092,507 (GRCm39) |
missense |
probably benign |
0.10 |
R6256:Myo7b
|
UTSW |
18 |
32,116,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R6257:Myo7b
|
UTSW |
18 |
32,146,468 (GRCm39) |
missense |
probably damaging |
1.00 |
R6265:Myo7b
|
UTSW |
18 |
32,131,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R6302:Myo7b
|
UTSW |
18 |
32,127,439 (GRCm39) |
missense |
probably damaging |
0.98 |
R6438:Myo7b
|
UTSW |
18 |
32,099,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R6654:Myo7b
|
UTSW |
18 |
32,123,322 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7030:Myo7b
|
UTSW |
18 |
32,104,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R7090:Myo7b
|
UTSW |
18 |
32,131,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R7210:Myo7b
|
UTSW |
18 |
32,140,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R7218:Myo7b
|
UTSW |
18 |
32,114,054 (GRCm39) |
missense |
probably benign |
0.05 |
R7378:Myo7b
|
UTSW |
18 |
32,099,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R7458:Myo7b
|
UTSW |
18 |
32,121,604 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7517:Myo7b
|
UTSW |
18 |
32,146,320 (GRCm39) |
missense |
probably damaging |
0.99 |
R7559:Myo7b
|
UTSW |
18 |
32,116,413 (GRCm39) |
missense |
probably benign |
0.01 |
R7667:Myo7b
|
UTSW |
18 |
32,094,958 (GRCm39) |
missense |
probably benign |
|
R7737:Myo7b
|
UTSW |
18 |
32,147,257 (GRCm39) |
nonsense |
probably null |
|
R7942:Myo7b
|
UTSW |
18 |
32,146,422 (GRCm39) |
missense |
probably damaging |
0.98 |
R8030:Myo7b
|
UTSW |
18 |
32,131,135 (GRCm39) |
missense |
probably damaging |
0.96 |
R8114:Myo7b
|
UTSW |
18 |
32,098,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R8338:Myo7b
|
UTSW |
18 |
32,104,408 (GRCm39) |
missense |
probably damaging |
0.96 |
R8341:Myo7b
|
UTSW |
18 |
32,116,979 (GRCm39) |
missense |
probably benign |
0.39 |
R8406:Myo7b
|
UTSW |
18 |
32,092,866 (GRCm39) |
missense |
probably damaging |
1.00 |
R8464:Myo7b
|
UTSW |
18 |
32,095,757 (GRCm39) |
missense |
probably benign |
0.00 |
R8517:Myo7b
|
UTSW |
18 |
32,100,244 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8537:Myo7b
|
UTSW |
18 |
32,110,142 (GRCm39) |
missense |
probably benign |
0.08 |
R8546:Myo7b
|
UTSW |
18 |
32,123,201 (GRCm39) |
missense |
probably benign |
0.19 |
R8721:Myo7b
|
UTSW |
18 |
32,140,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R8770:Myo7b
|
UTSW |
18 |
32,114,124 (GRCm39) |
missense |
probably benign |
0.03 |
R8841:Myo7b
|
UTSW |
18 |
32,097,490 (GRCm39) |
missense |
probably benign |
0.06 |
R8853:Myo7b
|
UTSW |
18 |
32,119,744 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8960:Myo7b
|
UTSW |
18 |
32,127,299 (GRCm39) |
splice site |
probably benign |
|
R8984:Myo7b
|
UTSW |
18 |
32,099,402 (GRCm39) |
missense |
probably null |
0.68 |
R9356:Myo7b
|
UTSW |
18 |
32,110,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R9357:Myo7b
|
UTSW |
18 |
32,093,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R9364:Myo7b
|
UTSW |
18 |
32,133,413 (GRCm39) |
missense |
probably benign |
0.12 |
R9405:Myo7b
|
UTSW |
18 |
32,109,356 (GRCm39) |
missense |
probably benign |
0.00 |
R9533:Myo7b
|
UTSW |
18 |
32,108,297 (GRCm39) |
missense |
probably benign |
0.27 |
R9776:Myo7b
|
UTSW |
18 |
32,133,068 (GRCm39) |
missense |
probably benign |
0.45 |
X0027:Myo7b
|
UTSW |
18 |
32,098,689 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Myo7b
|
UTSW |
18 |
32,114,051 (GRCm39) |
missense |
possibly damaging |
0.82 |
Z1177:Myo7b
|
UTSW |
18 |
32,118,109 (GRCm39) |
missense |
probably damaging |
1.00 |
|