Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsl6 |
G |
T |
11: 54,227,840 (GRCm39) |
|
probably null |
Het |
Anapc5 |
A |
G |
5: 122,957,716 (GRCm39) |
L69P |
possibly damaging |
Het |
Aoc1l3 |
CCTAAATTTCCTATCCCGATCAGCAAGGGTGGCCCTCGAGTGCCCCAGCCCCATGCTAAATTTCC |
CCTAAATTTCC |
6: 48,965,074 (GRCm39) |
|
probably benign |
Het |
Arfgef1 |
A |
T |
1: 10,259,055 (GRCm39) |
S681T |
probably benign |
Het |
Arhgef19 |
A |
G |
4: 140,976,549 (GRCm39) |
D437G |
probably damaging |
Het |
Arhgef25 |
A |
G |
10: 127,019,089 (GRCm39) |
V576A |
probably benign |
Het |
Arl5b |
T |
C |
2: 15,073,012 (GRCm39) |
|
probably null |
Het |
Atg10 |
T |
A |
13: 91,189,071 (GRCm39) |
T80S |
probably benign |
Het |
BC034090 |
A |
G |
1: 155,117,419 (GRCm39) |
V233A |
possibly damaging |
Het |
Bicdl2 |
C |
T |
17: 23,887,158 (GRCm39) |
R482C |
probably damaging |
Het |
Ccdc63 |
G |
A |
5: 122,247,346 (GRCm39) |
P500S |
probably benign |
Het |
Ccn2 |
A |
T |
10: 24,472,647 (GRCm39) |
T186S |
probably benign |
Het |
Ccng1 |
A |
T |
11: 40,643,078 (GRCm39) |
I123K |
possibly damaging |
Het |
Ccp110 |
C |
T |
7: 118,324,680 (GRCm39) |
S734F |
probably damaging |
Het |
Cds2 |
T |
C |
2: 132,139,614 (GRCm39) |
|
probably null |
Het |
Cenpw |
G |
A |
10: 30,074,523 (GRCm39) |
T58I |
probably benign |
Het |
Cfap61 |
T |
A |
2: 145,850,839 (GRCm39) |
L326I |
probably benign |
Het |
Cgn |
T |
A |
3: 94,674,551 (GRCm39) |
Q862L |
possibly damaging |
Het |
Cntrl |
T |
A |
2: 35,016,071 (GRCm39) |
D362E |
probably damaging |
Het |
Col22a1 |
C |
T |
15: 71,762,431 (GRCm39) |
G76E |
probably damaging |
Het |
Cplane1 |
C |
T |
15: 8,252,622 (GRCm39) |
T1948I |
possibly damaging |
Het |
Crip2 |
A |
G |
12: 113,108,030 (GRCm39) |
T140A |
probably benign |
Het |
Csde1 |
T |
C |
3: 102,950,976 (GRCm39) |
V229A |
probably damaging |
Het |
Cyp2d34 |
A |
G |
15: 82,500,523 (GRCm39) |
F439L |
probably damaging |
Het |
Dync1h1 |
A |
G |
12: 110,606,186 (GRCm39) |
T2419A |
probably benign |
Het |
Dync2h1 |
A |
T |
9: 7,051,495 (GRCm39) |
F3147I |
probably damaging |
Het |
Dynlt1f |
T |
C |
17: 6,916,707 (GRCm39) |
T101A |
probably benign |
Het |
Efcab3 |
A |
G |
11: 104,927,601 (GRCm39) |
H4790R |
probably benign |
Het |
Efcab8 |
G |
A |
2: 153,622,888 (GRCm39) |
S19N |
|
Het |
Eno2 |
A |
T |
6: 124,740,091 (GRCm39) |
I315K |
possibly damaging |
Het |
Erich3 |
A |
G |
3: 154,468,886 (GRCm39) |
T1113A |
unknown |
Het |
Fam217a |
A |
T |
13: 35,095,007 (GRCm39) |
Y251N |
possibly damaging |
Het |
Fcrlb |
A |
T |
1: 170,734,938 (GRCm39) |
H396Q |
probably benign |
Het |
Fcsk |
A |
G |
8: 111,614,064 (GRCm39) |
V693A |
probably benign |
Het |
Fgd5 |
A |
T |
6: 92,046,447 (GRCm39) |
K1397* |
probably null |
Het |
Frem1 |
C |
A |
4: 82,831,785 (GRCm39) |
L2010F |
probably benign |
Het |
Fzd8 |
A |
G |
18: 9,214,661 (GRCm39) |
Y581C |
probably damaging |
Het |
Gcc2 |
T |
C |
10: 58,106,411 (GRCm39) |
V549A |
possibly damaging |
Het |
Gcnt4 |
G |
A |
13: 97,083,042 (GRCm39) |
V113I |
probably benign |
Het |
Gldn |
A |
G |
9: 54,245,747 (GRCm39) |
I433V |
probably benign |
Het |
Gm3336 |
A |
G |
8: 71,173,069 (GRCm39) |
D27G |
unknown |
Het |
Gm6133 |
T |
A |
18: 78,393,146 (GRCm39) |
Y47N |
probably damaging |
Het |
Gm8257 |
A |
T |
14: 44,893,877 (GRCm39) |
N62K |
probably benign |
Het |
Gpr18 |
T |
G |
14: 122,149,667 (GRCm39) |
R119S |
probably damaging |
Het |
Grm5 |
A |
T |
7: 87,685,397 (GRCm39) |
I505F |
possibly damaging |
Het |
Hdgfl1 |
T |
C |
13: 26,953,428 (GRCm39) |
E215G |
probably benign |
Het |
Heg1 |
T |
A |
16: 33,527,339 (GRCm39) |
C100S |
probably benign |
Het |
Isg20l2 |
T |
C |
3: 87,839,302 (GRCm39) |
V171A |
probably benign |
Het |
Lrrc49 |
A |
T |
9: 60,495,150 (GRCm39) |
C694S |
probably benign |
Het |
Map7d1 |
A |
T |
4: 126,133,911 (GRCm39) |
I217N |
probably damaging |
Het |
Mbnl2 |
A |
T |
14: 120,562,712 (GRCm39) |
Q21L |
probably benign |
Het |
Mfsd10 |
A |
T |
5: 34,792,751 (GRCm39) |
F220Y |
probably benign |
Het |
Mmp1b |
A |
C |
9: 7,387,909 (GRCm39) |
N28K |
probably null |
Het |
Muc16 |
A |
T |
9: 18,555,975 (GRCm39) |
N3439K |
unknown |
Het |
Myef2l |
C |
A |
3: 10,157,341 (GRCm39) |
Q495K |
unknown |
Het |
Mysm1 |
T |
C |
4: 94,835,294 (GRCm39) |
T790A |
probably benign |
Het |
Nell2 |
C |
T |
15: 95,194,117 (GRCm39) |
C532Y |
probably damaging |
Het |
Nmnat1 |
T |
A |
4: 149,553,482 (GRCm39) |
N210I |
probably damaging |
Het |
Or14j7 |
T |
G |
17: 38,235,168 (GRCm39) |
V237G |
probably benign |
Het |
Or2aj6 |
A |
T |
16: 19,443,295 (GRCm39) |
L185* |
probably null |
Het |
Or4k41 |
T |
C |
2: 111,280,343 (GRCm39) |
I286T |
probably damaging |
Het |
Or7g16 |
G |
A |
9: 18,727,569 (GRCm39) |
T7I |
probably damaging |
Het |
Pabpc6 |
T |
C |
17: 9,888,281 (GRCm39) |
D90G |
probably damaging |
Het |
Pacs2 |
A |
T |
12: 113,026,104 (GRCm39) |
I554F |
possibly damaging |
Het |
Padi3 |
C |
A |
4: 140,523,004 (GRCm39) |
V323L |
probably benign |
Het |
Piezo1 |
G |
A |
8: 123,215,090 (GRCm39) |
P1484L |
|
Het |
Pogk |
A |
G |
1: 166,227,254 (GRCm39) |
I299T |
possibly damaging |
Het |
Ptprk |
A |
G |
10: 28,461,928 (GRCm39) |
I1164V |
probably benign |
Het |
Raph1 |
A |
G |
1: 60,542,124 (GRCm39) |
M278T |
unknown |
Het |
Rasa3 |
T |
A |
8: 13,645,851 (GRCm39) |
Q163L |
probably benign |
Het |
Rbm6 |
T |
A |
9: 107,660,911 (GRCm39) |
K884I |
probably damaging |
Het |
Rtl1 |
A |
G |
12: 109,559,691 (GRCm39) |
V716A |
probably benign |
Het |
Sag |
A |
G |
1: 87,749,054 (GRCm39) |
K151R |
probably damaging |
Het |
Scara5 |
G |
A |
14: 66,000,197 (GRCm39) |
V456M |
probably benign |
Het |
Selplg |
GTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCT |
GTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCTGCCTCCATGGGTGCTGGCTGCGAGGTCTCT |
5: 113,957,756 (GRCm39) |
|
probably benign |
Het |
Slc4a1 |
A |
T |
11: 102,243,279 (GRCm39) |
V784D |
probably damaging |
Het |
Sstr1 |
T |
C |
12: 58,259,569 (GRCm39) |
I64T |
possibly damaging |
Het |
Steap1 |
A |
G |
5: 5,790,708 (GRCm39) |
I80T |
probably benign |
Het |
Tbc1d24 |
T |
A |
17: 24,427,491 (GRCm39) |
D157V |
probably benign |
Het |
Thsd7a |
T |
C |
6: 12,418,249 (GRCm39) |
E660G |
|
Het |
Trappc3l |
A |
G |
10: 33,932,786 (GRCm39) |
|
probably benign |
Het |
Tsc22d2 |
T |
C |
3: 58,323,497 (GRCm39) |
S130P |
probably benign |
Het |
Tti2 |
T |
A |
8: 31,645,814 (GRCm39) |
I376N |
probably damaging |
Het |
Ttll2 |
C |
A |
17: 7,619,054 (GRCm39) |
W291L |
probably benign |
Het |
Ttll3 |
G |
A |
6: 113,376,657 (GRCm39) |
V345I |
possibly damaging |
Het |
Ttn |
A |
G |
2: 76,565,046 (GRCm39) |
Y28394H |
probably damaging |
Het |
Usp45 |
A |
G |
4: 21,832,201 (GRCm39) |
Y684C |
probably damaging |
Het |
Vdr |
A |
G |
15: 97,765,089 (GRCm39) |
S217P |
probably benign |
Het |
Xpot |
A |
G |
10: 121,447,580 (GRCm39) |
L105P |
probably damaging |
Het |
Zan |
A |
G |
5: 137,464,206 (GRCm39) |
I533T |
probably damaging |
Het |
Zbtb8a |
T |
C |
4: 129,248,059 (GRCm39) |
E404G |
probably benign |
Het |
Zfp106 |
T |
A |
2: 120,369,906 (GRCm39) |
I62F |
probably damaging |
Het |
Zfp451 |
A |
T |
1: 33,815,562 (GRCm39) |
F796Y |
probably damaging |
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 |
R0521:Myo9a
|
UTSW |
9 |
59,801,635 (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 |
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 |
|