Other mutations in this stock |
Total: 91 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ackr1 |
T |
A |
1: 173,160,075 (GRCm39) |
Y148F |
possibly damaging |
Het |
Adamtsl3 |
A |
G |
7: 82,244,722 (GRCm39) |
T1393A |
probably benign |
Het |
Adgrf4 |
G |
T |
17: 42,978,258 (GRCm39) |
Q362K |
probably benign |
Het |
Akr1d1 |
A |
G |
6: 37,531,451 (GRCm39) |
K163R |
probably benign |
Het |
Arhgap42 |
A |
G |
9: 9,011,364 (GRCm39) |
L474P |
probably damaging |
Het |
Arhgef18 |
G |
A |
8: 3,487,007 (GRCm39) |
R242Q |
possibly damaging |
Het |
Asah1 |
A |
G |
8: 41,807,049 (GRCm39) |
|
probably null |
Het |
Atm |
A |
T |
9: 53,445,044 (GRCm39) |
I34N |
probably benign |
Het |
Brms1l |
A |
G |
12: 55,906,913 (GRCm39) |
E160G |
possibly damaging |
Het |
Camk2a |
C |
T |
18: 61,076,327 (GRCm39) |
H102Y |
unknown |
Het |
Cd300lb |
A |
G |
11: 114,819,134 (GRCm39) |
V165A |
probably damaging |
Het |
Cela1 |
G |
A |
15: 100,579,038 (GRCm39) |
R207C |
probably benign |
Het |
Chd7 |
T |
C |
4: 8,785,642 (GRCm39) |
S649P |
|
Het |
Cilk1 |
A |
T |
9: 78,074,230 (GRCm39) |
S551C |
possibly damaging |
Het |
Clic3 |
A |
G |
2: 25,348,325 (GRCm39) |
Q130R |
probably benign |
Het |
Clns1a |
G |
A |
7: 97,363,125 (GRCm39) |
G166R |
probably damaging |
Het |
Cngb1 |
A |
T |
8: 95,979,893 (GRCm39) |
H1002Q |
probably benign |
Het |
Cnnm1 |
C |
A |
19: 43,429,839 (GRCm39) |
A319E |
probably benign |
Het |
Cntnap5b |
C |
T |
1: 99,978,368 (GRCm39) |
T128I |
probably benign |
Het |
Csf3r |
G |
A |
4: 125,923,813 (GRCm39) |
D108N |
probably benign |
Het |
Ctsc |
G |
A |
7: 87,959,016 (GRCm39) |
W432* |
probably null |
Het |
Dapk1 |
G |
A |
13: 60,909,208 (GRCm39) |
G1274R |
probably damaging |
Het |
Dennd2c |
C |
A |
3: 103,065,031 (GRCm39) |
P718Q |
probably damaging |
Het |
Dmxl1 |
C |
G |
18: 50,072,639 (GRCm39) |
N2744K |
probably damaging |
Het |
Dnah7b |
C |
T |
1: 46,266,180 (GRCm39) |
R2250C |
probably damaging |
Het |
Dnmt3a |
A |
T |
12: 3,916,136 (GRCm39) |
Q107L |
probably benign |
Het |
Eml2 |
A |
G |
7: 18,918,751 (GRCm39) |
D67G |
|
Het |
Eml5 |
A |
T |
12: 98,825,099 (GRCm39) |
V706E |
probably damaging |
Het |
Eps8l1 |
A |
G |
7: 4,480,573 (GRCm39) |
D509G |
|
Het |
Farsb |
T |
C |
1: 78,459,951 (GRCm39) |
K43E |
probably benign |
Het |
Fbxw20 |
A |
G |
9: 109,052,514 (GRCm39) |
F273S |
probably damaging |
Het |
Fig4 |
A |
T |
10: 41,141,407 (GRCm39) |
F284Y |
possibly damaging |
Het |
Fsd1l |
C |
A |
4: 53,694,756 (GRCm39) |
N403K |
probably damaging |
Het |
Fsip2 |
A |
T |
2: 82,813,170 (GRCm39) |
H3163L |
probably benign |
Het |
Gm38119 |
C |
A |
3: 92,645,403 (GRCm39) |
G64* |
probably null |
Het |
Gpr18 |
A |
G |
14: 122,149,173 (GRCm39) |
V284A |
probably benign |
Het |
Hacd3 |
A |
G |
9: 64,908,286 (GRCm39) |
V170A |
probably damaging |
Het |
Hps3 |
T |
C |
3: 20,083,350 (GRCm39) |
E281G |
probably damaging |
Het |
Ighv12-3 |
A |
C |
12: 114,330,546 (GRCm39) |
V10G |
probably benign |
Het |
Lrp1b |
G |
A |
2: 40,589,590 (GRCm39) |
R3862* |
probably null |
Het |
Ltbp4 |
A |
G |
7: 27,036,976 (GRCm39) |
L6P |
unknown |
Het |
Ly6h |
T |
A |
15: 75,437,522 (GRCm39) |
T53S |
probably damaging |
Het |
Ly6i |
A |
G |
15: 74,855,006 (GRCm39) |
|
probably benign |
Het |
Mat2a |
G |
A |
6: 72,413,227 (GRCm39) |
R168C |
probably damaging |
Het |
Mdn1 |
T |
A |
4: 32,762,275 (GRCm39) |
D5066E |
possibly damaging |
Het |
Med23 |
T |
A |
10: 24,780,279 (GRCm39) |
F976I |
|
Het |
Muc5ac |
T |
C |
7: 141,363,529 (GRCm39) |
I2280T |
unknown |
Het |
Mylk |
G |
T |
16: 34,776,835 (GRCm39) |
C1336F |
probably benign |
Het |
Naglu |
T |
A |
11: 100,967,731 (GRCm39) |
D560E |
probably damaging |
Het |
Nrg2 |
C |
T |
18: 36,157,396 (GRCm39) |
V430M |
probably damaging |
Het |
Oit3 |
T |
C |
10: 59,271,751 (GRCm39) |
N202S |
probably benign |
Het |
Or13a1 |
A |
G |
6: 116,470,881 (GRCm39) |
T104A |
probably benign |
Het |
Or1e29 |
A |
T |
11: 73,668,150 (GRCm39) |
M1K |
probably null |
Het |
Or52r1 |
T |
C |
7: 102,537,186 (GRCm39) |
H58R |
probably benign |
Het |
Or5b101 |
T |
A |
19: 13,005,360 (GRCm39) |
Y111F |
probably benign |
Het |
Or6c63-ps1 |
C |
A |
10: 128,899,097 (GRCm39) |
V260F |
probably damaging |
Het |
Otog |
T |
A |
7: 45,952,597 (GRCm39) |
C423* |
probably null |
Het |
Pcolce |
T |
A |
5: 137,603,770 (GRCm39) |
T401S |
probably benign |
Het |
Pcsk2 |
T |
C |
2: 143,655,583 (GRCm39) |
M589T |
possibly damaging |
Het |
Pik3r5 |
T |
C |
11: 68,383,099 (GRCm39) |
L306P |
possibly damaging |
Het |
Pikfyve |
T |
A |
1: 65,285,239 (GRCm39) |
M826K |
probably damaging |
Het |
Ppp1r9a |
A |
G |
6: 5,134,106 (GRCm39) |
R898G |
possibly damaging |
Het |
Prl7b1 |
A |
G |
13: 27,790,968 (GRCm39) |
V39A |
probably benign |
Het |
Pros1 |
T |
A |
16: 62,748,397 (GRCm39) |
D623E |
probably damaging |
Het |
Psg16 |
A |
G |
7: 16,832,024 (GRCm39) |
D320G |
probably benign |
Het |
Ptpre |
T |
A |
7: 135,280,875 (GRCm39) |
H612Q |
probably damaging |
Het |
Rbm34 |
A |
G |
8: 127,679,928 (GRCm39) |
S283P |
probably damaging |
Het |
Rc3h2 |
A |
T |
2: 37,304,702 (GRCm39) |
N19K |
possibly damaging |
Het |
Sacm1l |
T |
A |
9: 123,381,827 (GRCm39) |
L143* |
probably null |
Het |
Septin9 |
T |
A |
11: 117,181,460 (GRCm39) |
S105T |
probably damaging |
Het |
Shprh |
T |
C |
10: 11,038,589 (GRCm39) |
M448T |
possibly damaging |
Het |
Slc6a20a |
A |
C |
9: 123,466,063 (GRCm39) |
*593E |
probably null |
Het |
Smarcc1 |
A |
G |
9: 109,964,710 (GRCm39) |
D89G |
possibly damaging |
Het |
Svep1 |
T |
A |
4: 58,087,778 (GRCm39) |
Y1767F |
possibly damaging |
Het |
Tanc2 |
T |
C |
11: 105,689,603 (GRCm39) |
V255A |
probably benign |
Het |
Tiam1 |
A |
G |
16: 89,657,155 (GRCm39) |
S694P |
probably damaging |
Het |
Tmem130 |
T |
C |
5: 144,680,529 (GRCm39) |
T292A |
|
Het |
Tob1 |
ACAGCAGCAGCAGCAGCAGCAGC |
ACAGCAGCAGCAGCAGCAGC |
11: 94,105,203 (GRCm39) |
|
probably benign |
Het |
Tpcn2 |
A |
G |
7: 144,814,662 (GRCm39) |
Y480H |
probably damaging |
Het |
Trf |
G |
T |
9: 103,089,087 (GRCm39) |
A600D |
probably damaging |
Het |
Ttc16 |
A |
T |
2: 32,659,232 (GRCm39) |
L346Q |
probably damaging |
Het |
Vars1 |
A |
C |
17: 35,223,773 (GRCm39) |
K229N |
possibly damaging |
Het |
Vmn1r113 |
G |
T |
7: 20,521,342 (GRCm39) |
G45C |
probably damaging |
Het |
Vmn1r32 |
A |
G |
6: 66,530,020 (GRCm39) |
V252A |
probably benign |
Het |
Vmn2r93 |
A |
G |
17: 18,546,143 (GRCm39) |
T672A |
probably damaging |
Het |
Wdfy4 |
T |
A |
14: 32,819,807 (GRCm39) |
T1466S |
|
Het |
Zcwpw1 |
T |
C |
5: 137,809,182 (GRCm39) |
Y317H |
probably damaging |
Het |
Zfp169 |
T |
C |
13: 48,644,557 (GRCm39) |
E190G |
unknown |
Het |
Zfp273 |
A |
T |
13: 67,973,685 (GRCm39) |
H271L |
probably damaging |
Het |
Zfp764 |
C |
A |
7: 127,005,719 (GRCm39) |
E20* |
probably null |
Het |
Znfx1 |
A |
T |
2: 166,892,298 (GRCm39) |
N639K |
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 |
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 |
R9036:Myo9a
|
UTSW |
9 |
59,687,584 (GRCm39) |
nonsense |
probably null |
|
R9130:Myo9a
|
UTSW |
9 |
59,739,514 (GRCm39) |
missense |
probably damaging |
0.98 |
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 |
|