Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl3 |
A |
T |
4: 144,182,464 (GRCm39) |
S335T |
probably damaging |
Het |
Abcb1b |
G |
A |
5: 8,914,238 (GRCm39) |
A1203T |
probably damaging |
Het |
Acsbg3 |
T |
A |
17: 57,192,169 (GRCm39) |
Y577* |
probably null |
Het |
Agt |
C |
A |
8: 125,283,839 (GRCm39) |
E427* |
probably null |
Het |
Angel1 |
G |
A |
12: 86,769,681 (GRCm39) |
S193F |
probably benign |
Het |
Ankrd16 |
T |
C |
2: 11,794,692 (GRCm39) |
V359A |
probably benign |
Het |
Ankrd33b |
T |
C |
15: 31,367,432 (GRCm39) |
D36G |
probably damaging |
Het |
Ano8 |
A |
T |
8: 71,931,902 (GRCm39) |
C766S |
probably benign |
Het |
Asic1 |
C |
T |
15: 99,596,700 (GRCm39) |
R499C |
probably damaging |
Het |
Atpsckmt |
T |
G |
15: 31,606,103 (GRCm39) |
S20R |
probably benign |
Het |
Bank1 |
C |
T |
3: 135,919,703 (GRCm39) |
C364Y |
probably damaging |
Het |
Bmerb1 |
T |
A |
16: 13,804,676 (GRCm39) |
S8T |
possibly damaging |
Het |
Bpifa5 |
C |
A |
2: 154,008,869 (GRCm39) |
D223E |
probably benign |
Het |
Capn5 |
C |
T |
7: 97,782,089 (GRCm39) |
R217Q |
probably damaging |
Het |
Ccm2 |
G |
A |
11: 6,540,886 (GRCm39) |
S184N |
probably damaging |
Het |
Ces5a |
T |
A |
8: 94,252,286 (GRCm39) |
D202V |
probably damaging |
Het |
Clasrp |
A |
G |
7: 19,322,528 (GRCm39) |
I284T |
probably benign |
Het |
Cog7 |
C |
A |
7: 121,540,392 (GRCm39) |
|
probably null |
Het |
Col13a1 |
A |
T |
10: 61,698,525 (GRCm39) |
M512K |
unknown |
Het |
Cps1 |
A |
C |
1: 67,254,723 (GRCm39) |
D1304A |
probably benign |
Het |
Crhbp |
C |
A |
13: 95,580,403 (GRCm39) |
|
probably null |
Het |
Ctdspl2 |
T |
A |
2: 121,837,368 (GRCm39) |
C377* |
probably null |
Het |
Ctsl |
G |
A |
13: 64,513,032 (GRCm39) |
L297F |
possibly damaging |
Het |
Ddost |
A |
G |
4: 138,038,046 (GRCm39) |
T262A |
probably benign |
Het |
Ddx4 |
A |
T |
13: 112,761,313 (GRCm39) |
|
probably null |
Het |
Ddx54 |
A |
G |
5: 120,764,927 (GRCm39) |
I769V |
probably benign |
Het |
Dock1 |
T |
A |
7: 134,745,507 (GRCm39) |
I1463N |
probably benign |
Het |
Dsg3 |
T |
A |
18: 20,660,872 (GRCm39) |
Y404N |
possibly damaging |
Het |
Epb42 |
T |
A |
2: 120,859,631 (GRCm39) |
K186* |
probably null |
Het |
Farp2 |
A |
G |
1: 93,504,543 (GRCm39) |
|
probably null |
Het |
Fbxl9 |
A |
T |
8: 106,039,425 (GRCm39) |
L617Q |
probably damaging |
Het |
Fev |
C |
A |
1: 74,921,692 (GRCm39) |
R86L |
possibly damaging |
Het |
Foxb2 |
G |
T |
19: 16,849,820 (GRCm39) |
C395* |
probably null |
Het |
Foxn3 |
A |
G |
12: 99,175,765 (GRCm39) |
V261A |
probably benign |
Het |
Fsd1 |
A |
G |
17: 56,298,245 (GRCm39) |
D190G |
probably benign |
Het |
Gm9930 |
A |
T |
10: 9,410,547 (GRCm39) |
|
noncoding transcript |
Het |
Gsdma2 |
A |
T |
11: 98,545,727 (GRCm39) |
K260* |
probably null |
Het |
Hdac7 |
G |
A |
15: 97,704,380 (GRCm39) |
Q497* |
probably null |
Het |
Hic1 |
G |
A |
11: 75,057,713 (GRCm39) |
P392L |
possibly damaging |
Het |
Hk3 |
C |
T |
13: 55,162,239 (GRCm39) |
|
probably null |
Het |
Ifna6 |
G |
T |
4: 88,745,887 (GRCm39) |
V79F |
probably benign |
Het |
Il20ra |
A |
T |
10: 19,635,388 (GRCm39) |
Q543L |
probably damaging |
Het |
Itk |
T |
A |
11: 46,251,115 (GRCm39) |
D163V |
probably damaging |
Het |
Kcnu1 |
T |
G |
8: 26,400,916 (GRCm39) |
L688R |
probably damaging |
Het |
Kdm5b |
T |
A |
1: 134,545,771 (GRCm39) |
S977R |
possibly damaging |
Het |
Kng1 |
G |
A |
16: 22,879,232 (GRCm39) |
A45T |
possibly damaging |
Het |
Map1a |
T |
G |
2: 121,136,234 (GRCm39) |
L2350R |
probably damaging |
Het |
Mdfic |
A |
G |
6: 15,799,755 (GRCm39) |
D212G |
probably benign |
Het |
Ms4a1 |
C |
A |
19: 11,236,043 (GRCm39) |
|
probably null |
Het |
Nbea |
A |
T |
3: 55,915,689 (GRCm39) |
W928R |
probably damaging |
Het |
Nfatc2ip |
T |
G |
7: 125,995,751 (GRCm39) |
D46A |
possibly damaging |
Het |
Ngly1 |
C |
T |
14: 16,290,774 (GRCm38) |
Q419* |
probably null |
Het |
Nsd2 |
T |
A |
5: 34,000,682 (GRCm39) |
N66K |
probably damaging |
Het |
Nsmce4a |
T |
C |
7: 130,138,732 (GRCm39) |
H304R |
probably damaging |
Het |
Odad2 |
G |
A |
18: 7,222,676 (GRCm39) |
P531L |
possibly damaging |
Het |
Or10a2 |
T |
A |
7: 106,673,965 (GRCm39) |
L310Q |
possibly damaging |
Het |
Or2y11 |
C |
T |
11: 49,443,291 (GRCm39) |
T239M |
probably damaging |
Het |
Or4a2 |
T |
C |
2: 89,248,544 (GRCm39) |
Y71C |
probably damaging |
Het |
Or51v8 |
T |
A |
7: 103,319,696 (GRCm39) |
I181F |
possibly damaging |
Het |
Or7e168 |
G |
A |
9: 19,720,156 (GRCm39) |
V181I |
probably benign |
Het |
Or8c20 |
A |
C |
9: 38,260,499 (GRCm39) |
N40T |
probably damaging |
Het |
Or8h9 |
C |
T |
2: 86,789,190 (GRCm39) |
G204D |
probably damaging |
Het |
Peg3 |
T |
C |
7: 6,714,427 (GRCm39) |
E265G |
probably damaging |
Het |
Pkd1 |
A |
G |
17: 24,814,193 (GRCm39) |
S4188G |
probably benign |
Het |
Pramel32 |
A |
T |
4: 88,547,559 (GRCm39) |
N37K |
probably damaging |
Het |
R3hdm1 |
G |
A |
1: 128,121,440 (GRCm39) |
V315I |
probably benign |
Het |
Rab24 |
A |
T |
13: 55,468,738 (GRCm39) |
|
probably null |
Het |
Rap1gap2 |
A |
T |
11: 74,332,592 (GRCm39) |
M71K |
probably damaging |
Het |
Rergl |
T |
G |
6: 139,473,524 (GRCm39) |
K42T |
probably damaging |
Het |
Septin5 |
T |
C |
16: 18,443,647 (GRCm39) |
T92A |
probably benign |
Het |
Setdb1 |
A |
G |
3: 95,246,140 (GRCm39) |
V595A |
probably benign |
Het |
Slc17a8 |
A |
G |
10: 89,412,192 (GRCm39) |
S414P |
probably benign |
Het |
Thnsl2 |
A |
T |
6: 71,111,243 (GRCm39) |
D208E |
probably damaging |
Het |
Tie1 |
A |
C |
4: 118,333,343 (GRCm39) |
I841R |
probably damaging |
Het |
Tll1 |
T |
G |
8: 64,551,505 (GRCm39) |
D292A |
probably damaging |
Het |
Tnfaip8l1 |
A |
T |
17: 56,478,727 (GRCm39) |
T6S |
probably damaging |
Het |
Trim17 |
T |
A |
11: 58,859,320 (GRCm39) |
V178E |
probably damaging |
Het |
Ttc27 |
A |
T |
17: 75,163,544 (GRCm39) |
R717S |
possibly damaging |
Het |
Upk2 |
G |
T |
9: 44,365,418 (GRCm39) |
P50Q |
probably damaging |
Het |
Usp9y |
A |
T |
Y: 1,307,880 (GRCm39) |
C2319S |
probably benign |
Het |
Vmn2r100 |
A |
T |
17: 19,742,178 (GRCm39) |
D184V |
probably damaging |
Het |
Vmn2r9 |
C |
A |
5: 108,996,154 (GRCm39) |
G165* |
probably null |
Het |
Xkr6 |
A |
T |
14: 64,056,871 (GRCm39) |
I261F |
probably benign |
Het |
Xpnpep3 |
T |
G |
15: 81,311,693 (GRCm39) |
I133S |
possibly damaging |
Het |
Yipf1 |
A |
G |
4: 107,193,387 (GRCm39) |
Y91C |
probably benign |
Het |
Zfp442 |
T |
C |
2: 150,253,169 (GRCm39) |
D31G |
possibly damaging |
Het |
Zfp628 |
A |
T |
7: 4,922,939 (GRCm39) |
Q387L |
probably damaging |
Het |
Zfp804a |
C |
T |
2: 82,089,761 (GRCm39) |
Q1197* |
probably null |
Het |
Zic2 |
CCCACCACCACCATCACCACCACCACC |
CCCACCATCACCACCACCACC |
14: 122,713,776 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Myo9a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00427:Myo9a
|
APN |
9 |
59,750,342 (GRCm39) |
splice site |
probably benign |
|
IGL00510:Myo9a
|
APN |
9 |
59,739,464 (GRCm39) |
splice site |
probably benign |
|
IGL00710:Myo9a
|
APN |
9 |
59,782,594 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00963:Myo9a
|
APN |
9 |
59,807,655 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01087:Myo9a
|
APN |
9 |
59,697,361 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01145:Myo9a
|
APN |
9 |
59,762,658 (GRCm39) |
missense |
probably benign |
0.18 |
IGL01403:Myo9a
|
APN |
9 |
59,778,846 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01528:Myo9a
|
APN |
9 |
59,686,957 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01608:Myo9a
|
APN |
9 |
59,778,119 (GRCm39) |
nonsense |
probably null |
|
IGL01701:Myo9a
|
APN |
9 |
59,791,877 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01918:Myo9a
|
APN |
9 |
59,686,985 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02026:Myo9a
|
APN |
9 |
59,813,245 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02139:Myo9a
|
APN |
9 |
59,687,275 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02176:Myo9a
|
APN |
9 |
59,777,836 (GRCm39) |
missense |
probably benign |
0.45 |
IGL02272:Myo9a
|
APN |
9 |
59,791,883 (GRCm39) |
splice site |
probably benign |
|
IGL02283:Myo9a
|
APN |
9 |
59,778,956 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02499:Myo9a
|
APN |
9 |
59,722,669 (GRCm39) |
splice site |
probably benign |
|
IGL02652:Myo9a
|
APN |
9 |
59,771,211 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02666:Myo9a
|
APN |
9 |
59,832,187 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02878:Myo9a
|
APN |
9 |
59,815,583 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02982:Myo9a
|
APN |
9 |
59,815,491 (GRCm39) |
nonsense |
probably null |
|
IGL03072:Myo9a
|
APN |
9 |
59,716,725 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL03090:Myo9a
|
APN |
9 |
59,801,418 (GRCm39) |
splice site |
probably benign |
|
IGL03111:Myo9a
|
APN |
9 |
59,734,526 (GRCm39) |
missense |
probably benign |
0.19 |
IGL03389:Myo9a
|
APN |
9 |
59,776,890 (GRCm39) |
missense |
probably damaging |
1.00 |
essentials
|
UTSW |
9 |
59,802,149 (GRCm39) |
missense |
probably benign |
0.09 |
necessities
|
UTSW |
9 |
59,722,617 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4402001:Myo9a
|
UTSW |
9 |
59,777,719 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0013:Myo9a
|
UTSW |
9 |
59,767,489 (GRCm39) |
splice site |
probably benign |
|
R0013:Myo9a
|
UTSW |
9 |
59,767,489 (GRCm39) |
splice site |
probably benign |
|
R0018:Myo9a
|
UTSW |
9 |
59,779,007 (GRCm39) |
missense |
probably benign |
0.00 |
R0018:Myo9a
|
UTSW |
9 |
59,779,007 (GRCm39) |
missense |
probably benign |
0.00 |
R0329:Myo9a
|
UTSW |
9 |
59,830,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R0423:Myo9a
|
UTSW |
9 |
59,802,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R0607:Myo9a
|
UTSW |
9 |
59,829,076 (GRCm39) |
missense |
probably benign |
0.02 |
R0652:Myo9a
|
UTSW |
9 |
59,779,209 (GRCm39) |
missense |
probably benign |
|
R0653:Myo9a
|
UTSW |
9 |
59,832,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R0723:Myo9a
|
UTSW |
9 |
59,778,383 (GRCm39) |
missense |
probably benign |
0.01 |
R0784:Myo9a
|
UTSW |
9 |
59,803,828 (GRCm39) |
splice site |
probably benign |
|
R0842:Myo9a
|
UTSW |
9 |
59,778,350 (GRCm39) |
missense |
probably benign |
0.02 |
R1055:Myo9a
|
UTSW |
9 |
59,762,653 (GRCm39) |
missense |
probably benign |
0.01 |
R1056:Myo9a
|
UTSW |
9 |
59,739,484 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1195:Myo9a
|
UTSW |
9 |
59,802,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R1195:Myo9a
|
UTSW |
9 |
59,802,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R1195:Myo9a
|
UTSW |
9 |
59,802,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R1615:Myo9a
|
UTSW |
9 |
59,695,739 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1698:Myo9a
|
UTSW |
9 |
59,775,464 (GRCm39) |
missense |
probably benign |
0.05 |
R1715:Myo9a
|
UTSW |
9 |
59,739,583 (GRCm39) |
missense |
probably damaging |
0.99 |
R1981:Myo9a
|
UTSW |
9 |
59,801,429 (GRCm39) |
missense |
probably benign |
|
R2228:Myo9a
|
UTSW |
9 |
59,801,463 (GRCm39) |
missense |
probably benign |
0.06 |
R2272:Myo9a
|
UTSW |
9 |
59,722,584 (GRCm39) |
missense |
probably damaging |
1.00 |
R2327:Myo9a
|
UTSW |
9 |
59,687,048 (GRCm39) |
missense |
probably benign |
0.11 |
R2990:Myo9a
|
UTSW |
9 |
59,832,172 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3161:Myo9a
|
UTSW |
9 |
59,739,598 (GRCm39) |
splice site |
probably benign |
|
R3721:Myo9a
|
UTSW |
9 |
59,775,463 (GRCm39) |
missense |
probably benign |
|
R3928:Myo9a
|
UTSW |
9 |
59,802,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R4197:Myo9a
|
UTSW |
9 |
59,802,149 (GRCm39) |
missense |
probably benign |
0.09 |
R4212:Myo9a
|
UTSW |
9 |
59,813,349 (GRCm39) |
nonsense |
probably null |
|
R4610:Myo9a
|
UTSW |
9 |
59,779,165 (GRCm39) |
missense |
probably benign |
|
R4616:Myo9a
|
UTSW |
9 |
59,728,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R4621:Myo9a
|
UTSW |
9 |
59,778,355 (GRCm39) |
missense |
probably benign |
0.00 |
R4623:Myo9a
|
UTSW |
9 |
59,778,355 (GRCm39) |
missense |
probably benign |
0.00 |
R4632:Myo9a
|
UTSW |
9 |
59,776,947 (GRCm39) |
missense |
probably benign |
0.00 |
R4657:Myo9a
|
UTSW |
9 |
59,782,699 (GRCm39) |
critical splice donor site |
probably null |
|
R4892:Myo9a
|
UTSW |
9 |
59,731,525 (GRCm39) |
missense |
probably damaging |
0.98 |
R4897:Myo9a
|
UTSW |
9 |
59,803,800 (GRCm39) |
missense |
probably benign |
0.07 |
R4966:Myo9a
|
UTSW |
9 |
59,779,017 (GRCm39) |
missense |
probably benign |
0.00 |
R4993:Myo9a
|
UTSW |
9 |
59,768,755 (GRCm39) |
nonsense |
probably null |
|
R5160:Myo9a
|
UTSW |
9 |
59,779,085 (GRCm39) |
missense |
probably benign |
0.24 |
R5233:Myo9a
|
UTSW |
9 |
59,817,900 (GRCm39) |
missense |
probably damaging |
1.00 |
R5271:Myo9a
|
UTSW |
9 |
59,814,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R5308:Myo9a
|
UTSW |
9 |
59,771,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R5367:Myo9a
|
UTSW |
9 |
59,807,732 (GRCm39) |
missense |
probably damaging |
0.96 |
R5432:Myo9a
|
UTSW |
9 |
59,772,953 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5459:Myo9a
|
UTSW |
9 |
59,791,803 (GRCm39) |
missense |
probably damaging |
0.98 |
R5511:Myo9a
|
UTSW |
9 |
59,687,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R5568:Myo9a
|
UTSW |
9 |
59,781,911 (GRCm39) |
missense |
probably benign |
|
R5573:Myo9a
|
UTSW |
9 |
59,778,284 (GRCm39) |
missense |
probably benign |
|
R5589:Myo9a
|
UTSW |
9 |
59,802,527 (GRCm39) |
nonsense |
probably null |
|
R5607:Myo9a
|
UTSW |
9 |
59,771,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R5633:Myo9a
|
UTSW |
9 |
59,775,467 (GRCm39) |
missense |
possibly damaging |
0.60 |
R5885:Myo9a
|
UTSW |
9 |
59,778,503 (GRCm39) |
missense |
probably benign |
|
R6024:Myo9a
|
UTSW |
9 |
59,762,671 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6086:Myo9a
|
UTSW |
9 |
59,697,340 (GRCm39) |
nonsense |
probably null |
|
R6146:Myo9a
|
UTSW |
9 |
59,778,512 (GRCm39) |
missense |
probably benign |
0.01 |
R6194:Myo9a
|
UTSW |
9 |
59,777,033 (GRCm39) |
missense |
probably benign |
0.00 |
R6213:Myo9a
|
UTSW |
9 |
59,734,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R6368:Myo9a
|
UTSW |
9 |
59,832,231 (GRCm39) |
missense |
probably benign |
0.01 |
R6550:Myo9a
|
UTSW |
9 |
59,775,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R6612:Myo9a
|
UTSW |
9 |
59,734,479 (GRCm39) |
missense |
probably damaging |
1.00 |
R6665:Myo9a
|
UTSW |
9 |
59,779,155 (GRCm39) |
missense |
probably benign |
0.09 |
R6951:Myo9a
|
UTSW |
9 |
59,802,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R7026:Myo9a
|
UTSW |
9 |
59,722,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R7107:Myo9a
|
UTSW |
9 |
59,778,098 (GRCm39) |
missense |
probably benign |
0.44 |
R7310:Myo9a
|
UTSW |
9 |
59,778,436 (GRCm39) |
missense |
probably benign |
0.08 |
R7473:Myo9a
|
UTSW |
9 |
59,802,527 (GRCm39) |
missense |
probably benign |
0.31 |
R7723:Myo9a
|
UTSW |
9 |
59,687,141 (GRCm39) |
missense |
probably damaging |
1.00 |
R7823:Myo9a
|
UTSW |
9 |
59,719,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R7824:Myo9a
|
UTSW |
9 |
59,767,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R7965:Myo9a
|
UTSW |
9 |
59,695,721 (GRCm39) |
missense |
probably damaging |
1.00 |
R8031:Myo9a
|
UTSW |
9 |
59,687,374 (GRCm39) |
missense |
probably benign |
0.33 |
R8055:Myo9a
|
UTSW |
9 |
59,814,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R8071:Myo9a
|
UTSW |
9 |
59,781,931 (GRCm39) |
missense |
probably benign |
|
R8250:Myo9a
|
UTSW |
9 |
59,767,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R8260:Myo9a
|
UTSW |
9 |
59,817,961 (GRCm39) |
missense |
probably benign |
0.08 |
R8355:Myo9a
|
UTSW |
9 |
59,817,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R8432:Myo9a
|
UTSW |
9 |
59,687,548 (GRCm39) |
missense |
probably damaging |
1.00 |
R8470:Myo9a
|
UTSW |
9 |
59,739,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R8528:Myo9a
|
UTSW |
9 |
59,767,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R8681:Myo9a
|
UTSW |
9 |
59,775,394 (GRCm39) |
missense |
probably benign |
0.16 |
R8690:Myo9a
|
UTSW |
9 |
59,782,657 (GRCm39) |
missense |
probably benign |
|
R8793:Myo9a
|
UTSW |
9 |
59,791,850 (GRCm39) |
missense |
probably benign |
0.03 |
R8812:Myo9a
|
UTSW |
9 |
59,687,030 (GRCm39) |
missense |
probably benign |
0.14 |
R9016:Myo9a
|
UTSW |
9 |
59,775,427 (GRCm39) |
nonsense |
probably null |
|
R9026:Myo9a
|
UTSW |
9 |
59,716,757 (GRCm39) |
missense |
probably damaging |
0.96 |
R9036:Myo9a
|
UTSW |
9 |
59,687,584 (GRCm39) |
nonsense |
probably null |
|
R9130:Myo9a
|
UTSW |
9 |
59,739,514 (GRCm39) |
missense |
probably damaging |
0.98 |
R9131:Myo9a
|
UTSW |
9 |
59,768,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R9213:Myo9a
|
UTSW |
9 |
59,772,922 (GRCm39) |
missense |
probably benign |
0.04 |
R9498:Myo9a
|
UTSW |
9 |
59,734,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R9575:Myo9a
|
UTSW |
9 |
59,813,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R9651:Myo9a
|
UTSW |
9 |
59,778,764 (GRCm39) |
missense |
probably damaging |
0.96 |
R9672:Myo9a
|
UTSW |
9 |
59,687,332 (GRCm39) |
missense |
probably benign |
0.16 |
RF018:Myo9a
|
UTSW |
9 |
59,776,869 (GRCm39) |
missense |
probably benign |
0.00 |
RF019:Myo9a
|
UTSW |
9 |
59,829,055 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Myo9a
|
UTSW |
9 |
59,802,542 (GRCm39) |
missense |
probably damaging |
1.00 |
|