Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
A |
C |
6: 121,645,158 (GRCm38) |
E340A |
possibly damaging |
Het |
Abca13 |
A |
G |
11: 9,314,507 (GRCm38) |
D2963G |
probably benign |
Het |
Actn3 |
T |
C |
19: 4,862,207 (GRCm38) |
D783G |
possibly damaging |
Het |
Adamtsl2 |
A |
G |
2: 27,103,127 (GRCm38) |
E723G |
possibly damaging |
Het |
Agrn |
G |
T |
4: 156,166,558 (GRCm38) |
Q1931K |
probably benign |
Het |
Ankrd27 |
G |
A |
7: 35,614,521 (GRCm38) |
A426T |
probably benign |
Het |
Atg9b |
C |
A |
5: 24,388,188 (GRCm38) |
G406C |
probably damaging |
Het |
BC005561 |
C |
T |
5: 104,520,510 (GRCm38) |
A966V |
probably benign |
Het |
C1ra |
A |
T |
6: 124,522,766 (GRCm38) |
Q637L |
probably benign |
Het |
Cdhr2 |
A |
T |
13: 54,719,581 (GRCm38) |
M438L |
probably benign |
Het |
Cep350 |
T |
C |
1: 155,953,358 (GRCm38) |
I267V |
possibly damaging |
Het |
Chrna5 |
A |
G |
9: 55,004,642 (GRCm38) |
Y138C |
probably damaging |
Het |
Chst3 |
T |
A |
10: 60,185,703 (GRCm38) |
M441L |
probably benign |
Het |
Cmya5 |
G |
A |
13: 93,063,519 (GRCm38) |
P3434S |
probably benign |
Het |
Cog2 |
T |
A |
8: 124,525,683 (GRCm38) |
L42Q |
probably damaging |
Het |
Cpq |
A |
T |
15: 33,250,126 (GRCm38) |
I210F |
probably benign |
Het |
Crnn |
C |
A |
3: 93,148,458 (GRCm38) |
Q184K |
probably damaging |
Het |
Csnka2ip |
A |
T |
16: 64,478,059 (GRCm38) |
Y647* |
probably null |
Het |
D5Ertd579e |
C |
T |
5: 36,604,530 (GRCm38) |
R1331H |
probably benign |
Het |
Dennd5a |
C |
T |
7: 109,917,380 (GRCm38) |
|
probably null |
Het |
Dync1h1 |
A |
G |
12: 110,626,992 (GRCm38) |
Q1231R |
possibly damaging |
Het |
Erbin |
T |
A |
13: 103,833,731 (GRCm38) |
I1126F |
possibly damaging |
Het |
Fastkd1 |
T |
C |
2: 69,702,469 (GRCm38) |
D518G |
probably benign |
Het |
Gcc1 |
A |
G |
6: 28,421,111 (GRCm38) |
L69P |
possibly damaging |
Het |
Gkn1 |
T |
C |
6: 87,347,169 (GRCm38) |
Y119C |
probably damaging |
Het |
Gmpr |
T |
G |
13: 45,517,044 (GRCm38) |
W81G |
probably benign |
Het |
Gyg |
T |
A |
3: 20,138,051 (GRCm38) |
I236F |
probably benign |
Het |
Hcrtr2 |
T |
C |
9: 76,246,453 (GRCm38) |
Y219C |
probably damaging |
Het |
Hmcn1 |
G |
A |
1: 150,565,369 (GRCm38) |
Q5379* |
probably null |
Het |
Kank1 |
T |
C |
19: 25,411,317 (GRCm38) |
C785R |
probably benign |
Het |
Lrp1b |
A |
T |
2: 40,851,806 (GRCm38) |
C3036* |
probably null |
Het |
Mdga2 |
T |
C |
12: 66,689,335 (GRCm38) |
D373G |
probably damaging |
Het |
Mgat2 |
A |
T |
12: 69,185,719 (GRCm38) |
I356F |
probably benign |
Het |
Miga2 |
A |
G |
2: 30,377,997 (GRCm38) |
D346G |
probably damaging |
Het |
Mprip |
T |
A |
11: 59,760,258 (GRCm38) |
L1596Q |
possibly damaging |
Het |
Mroh2b |
G |
A |
15: 4,914,140 (GRCm38) |
R386Q |
probably benign |
Het |
Mst1r |
T |
A |
9: 107,919,980 (GRCm38) |
S1349R |
probably benign |
Het |
Mtmr3 |
C |
T |
11: 4,492,825 (GRCm38) |
R403H |
possibly damaging |
Het |
Mycbpap |
G |
A |
11: 94,508,143 (GRCm38) |
Q460* |
probably null |
Het |
Ncapd2 |
C |
T |
6: 125,168,590 (GRCm38) |
E1365K |
probably null |
Het |
Nkiras2 |
C |
A |
11: 100,625,163 (GRCm38) |
D105E |
probably damaging |
Het |
Nolc1 |
T |
G |
19: 46,081,431 (GRCm38) |
|
probably null |
Het |
Nos1 |
T |
C |
5: 117,867,232 (GRCm38) |
F6L |
probably benign |
Het |
Olfr1112 |
G |
T |
2: 87,191,737 (GRCm38) |
V17L |
probably benign |
Het |
Olfr1278 |
T |
A |
2: 111,292,560 (GRCm38) |
C97* |
probably null |
Het |
Olfr1369-ps1 |
C |
T |
13: 21,116,565 (GRCm38) |
T291I |
probably benign |
Het |
Olfr218 |
A |
T |
1: 173,203,371 (GRCm38) |
N5I |
probably damaging |
Het |
Olfr325 |
T |
C |
11: 58,581,251 (GRCm38) |
Y136H |
probably damaging |
Het |
Olfr910 |
T |
A |
9: 38,539,256 (GRCm38) |
Y120* |
probably null |
Het |
Pfkm |
A |
G |
15: 98,128,318 (GRCm38) |
E598G |
possibly damaging |
Het |
Phf2 |
A |
T |
13: 48,807,630 (GRCm38) |
D861E |
unknown |
Het |
Polr2a |
A |
G |
11: 69,739,877 (GRCm38) |
|
probably null |
Het |
Popdc2 |
G |
A |
16: 38,369,491 (GRCm38) |
V167M |
probably damaging |
Het |
Ptpn22 |
T |
C |
3: 103,885,798 (GRCm38) |
S422P |
probably benign |
Het |
Rasa2 |
T |
C |
9: 96,568,375 (GRCm38) |
K490R |
possibly damaging |
Het |
Rbfox3 |
T |
A |
11: 118,495,221 (GRCm38) |
D286V |
probably damaging |
Het |
Rdh13 |
A |
G |
7: 4,427,791 (GRCm38) |
W223R |
probably damaging |
Het |
Riok3 |
T |
C |
18: 12,128,929 (GRCm38) |
S7P |
probably benign |
Het |
Rnaseh2b |
A |
G |
14: 62,353,632 (GRCm38) |
E144G |
probably benign |
Het |
Rnf20 |
C |
T |
4: 49,651,498 (GRCm38) |
Q655* |
probably null |
Het |
Rpap2 |
T |
C |
5: 107,603,550 (GRCm38) |
Y8H |
probably damaging |
Het |
Slc5a10 |
T |
C |
11: 61,709,602 (GRCm38) |
Y181C |
probably benign |
Het |
Snd1 |
G |
T |
6: 28,888,253 (GRCm38) |
G896* |
probably null |
Het |
Spast |
C |
T |
17: 74,356,160 (GRCm38) |
Q158* |
probably null |
Het |
Tas2r104 |
G |
A |
6: 131,685,584 (GRCm38) |
S54F |
probably damaging |
Het |
Tcaf2 |
C |
T |
6: 42,628,017 (GRCm38) |
W611* |
probably null |
Het |
Timp4 |
G |
A |
6: 115,250,403 (GRCm38) |
|
probably null |
Het |
Tmem45a |
G |
A |
16: 56,823,570 (GRCm38) |
S72L |
probably benign |
Het |
Tnrc18 |
T |
C |
5: 142,788,703 (GRCm38) |
T124A |
possibly damaging |
Het |
Tns2 |
C |
T |
15: 102,108,934 (GRCm38) |
R281C |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,942,915 (GRCm38) |
D2381G |
probably damaging |
Het |
Uevld |
T |
C |
7: 46,955,624 (GRCm38) |
T41A |
possibly damaging |
Het |
Ugcg |
C |
T |
4: 59,207,798 (GRCm38) |
P46S |
probably benign |
Het |
Unc5d |
T |
C |
8: 28,696,478 (GRCm38) |
E527G |
probably damaging |
Het |
Vmn2r125 |
C |
T |
4: 156,351,038 (GRCm38) |
T237I |
probably benign |
Het |
Vmn2r63 |
A |
C |
7: 42,933,614 (GRCm38) |
I59S |
probably benign |
Het |
Vps72 |
G |
A |
3: 95,118,695 (GRCm38) |
S106N |
probably benign |
Het |
Zan |
A |
C |
5: 137,409,669 (GRCm38) |
|
probably benign |
Het |
Zbtb38 |
T |
C |
9: 96,685,462 (GRCm38) |
K1190E |
probably benign |
Het |
Zc3h6 |
T |
C |
2: 129,017,358 (GRCm38) |
V1103A |
probably benign |
Het |
Zfp407 |
G |
A |
18: 84,562,157 (GRCm38) |
T277I |
probably damaging |
Het |
Zfp804b |
A |
G |
5: 6,769,509 (GRCm38) |
S1149P |
probably damaging |
Het |
|
Other mutations in Myo9a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00427:Myo9a
|
APN |
9 |
59,843,059 (GRCm38) |
splice site |
probably benign |
|
IGL00510:Myo9a
|
APN |
9 |
59,832,181 (GRCm38) |
splice site |
probably benign |
|
IGL00710:Myo9a
|
APN |
9 |
59,875,311 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL00963:Myo9a
|
APN |
9 |
59,900,372 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL01087:Myo9a
|
APN |
9 |
59,790,078 (GRCm38) |
missense |
possibly damaging |
0.93 |
IGL01145:Myo9a
|
APN |
9 |
59,855,375 (GRCm38) |
missense |
probably benign |
0.18 |
IGL01403:Myo9a
|
APN |
9 |
59,871,563 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL01528:Myo9a
|
APN |
9 |
59,779,674 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01608:Myo9a
|
APN |
9 |
59,870,836 (GRCm38) |
nonsense |
probably null |
|
IGL01701:Myo9a
|
APN |
9 |
59,884,594 (GRCm38) |
critical splice donor site |
probably null |
|
IGL01918:Myo9a
|
APN |
9 |
59,779,702 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02026:Myo9a
|
APN |
9 |
59,905,962 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL02139:Myo9a
|
APN |
9 |
59,779,992 (GRCm38) |
missense |
probably benign |
0.07 |
IGL02176:Myo9a
|
APN |
9 |
59,870,553 (GRCm38) |
missense |
probably benign |
0.45 |
IGL02272:Myo9a
|
APN |
9 |
59,884,600 (GRCm38) |
splice site |
probably benign |
|
IGL02283:Myo9a
|
APN |
9 |
59,871,673 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02499:Myo9a
|
APN |
9 |
59,815,386 (GRCm38) |
splice site |
probably benign |
|
IGL02652:Myo9a
|
APN |
9 |
59,863,928 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02666:Myo9a
|
APN |
9 |
59,924,904 (GRCm38) |
missense |
probably benign |
0.02 |
IGL02878:Myo9a
|
APN |
9 |
59,908,300 (GRCm38) |
critical splice donor site |
probably null |
|
IGL02982:Myo9a
|
APN |
9 |
59,908,208 (GRCm38) |
nonsense |
probably null |
|
IGL03072:Myo9a
|
APN |
9 |
59,809,442 (GRCm38) |
missense |
possibly damaging |
0.83 |
IGL03090:Myo9a
|
APN |
9 |
59,894,135 (GRCm38) |
splice site |
probably benign |
|
IGL03111:Myo9a
|
APN |
9 |
59,827,243 (GRCm38) |
missense |
probably benign |
0.19 |
IGL03389:Myo9a
|
APN |
9 |
59,869,607 (GRCm38) |
missense |
probably damaging |
1.00 |
essentials
|
UTSW |
9 |
59,894,866 (GRCm38) |
missense |
probably benign |
0.09 |
necessities
|
UTSW |
9 |
59,815,334 (GRCm38) |
missense |
probably damaging |
1.00 |
PIT4402001:Myo9a
|
UTSW |
9 |
59,870,436 (GRCm38) |
missense |
possibly damaging |
0.83 |
R0013:Myo9a
|
UTSW |
9 |
59,860,206 (GRCm38) |
splice site |
probably benign |
|
R0013:Myo9a
|
UTSW |
9 |
59,860,206 (GRCm38) |
splice site |
probably benign |
|
R0018:Myo9a
|
UTSW |
9 |
59,871,724 (GRCm38) |
missense |
probably benign |
0.00 |
R0018:Myo9a
|
UTSW |
9 |
59,871,724 (GRCm38) |
missense |
probably benign |
0.00 |
R0329:Myo9a
|
UTSW |
9 |
59,923,677 (GRCm38) |
missense |
probably damaging |
1.00 |
R0423:Myo9a
|
UTSW |
9 |
59,895,336 (GRCm38) |
missense |
probably damaging |
1.00 |
R0521:Myo9a
|
UTSW |
9 |
59,894,352 (GRCm38) |
missense |
probably damaging |
1.00 |
R0607:Myo9a
|
UTSW |
9 |
59,921,793 (GRCm38) |
missense |
probably benign |
0.02 |
R0652:Myo9a
|
UTSW |
9 |
59,871,926 (GRCm38) |
missense |
probably benign |
|
R0653:Myo9a
|
UTSW |
9 |
59,924,991 (GRCm38) |
missense |
probably damaging |
1.00 |
R0723:Myo9a
|
UTSW |
9 |
59,871,100 (GRCm38) |
missense |
probably benign |
0.01 |
R0784:Myo9a
|
UTSW |
9 |
59,896,545 (GRCm38) |
splice site |
probably benign |
|
R0842:Myo9a
|
UTSW |
9 |
59,871,067 (GRCm38) |
missense |
probably benign |
0.02 |
R1055:Myo9a
|
UTSW |
9 |
59,855,370 (GRCm38) |
missense |
probably benign |
0.01 |
R1056:Myo9a
|
UTSW |
9 |
59,832,201 (GRCm38) |
missense |
possibly damaging |
0.64 |
R1195:Myo9a
|
UTSW |
9 |
59,895,200 (GRCm38) |
missense |
probably damaging |
1.00 |
R1195:Myo9a
|
UTSW |
9 |
59,895,200 (GRCm38) |
missense |
probably damaging |
1.00 |
R1195:Myo9a
|
UTSW |
9 |
59,895,200 (GRCm38) |
missense |
probably damaging |
1.00 |
R1615:Myo9a
|
UTSW |
9 |
59,788,456 (GRCm38) |
missense |
possibly damaging |
0.68 |
R1715:Myo9a
|
UTSW |
9 |
59,832,300 (GRCm38) |
missense |
probably damaging |
0.99 |
R1981:Myo9a
|
UTSW |
9 |
59,894,146 (GRCm38) |
missense |
probably benign |
|
R2228:Myo9a
|
UTSW |
9 |
59,894,180 (GRCm38) |
missense |
probably benign |
0.06 |
R2272:Myo9a
|
UTSW |
9 |
59,815,301 (GRCm38) |
missense |
probably damaging |
1.00 |
R2327:Myo9a
|
UTSW |
9 |
59,779,765 (GRCm38) |
missense |
probably benign |
0.11 |
R2990:Myo9a
|
UTSW |
9 |
59,924,889 (GRCm38) |
missense |
possibly damaging |
0.95 |
R3161:Myo9a
|
UTSW |
9 |
59,832,315 (GRCm38) |
splice site |
probably benign |
|
R3721:Myo9a
|
UTSW |
9 |
59,868,180 (GRCm38) |
missense |
probably benign |
|
R3928:Myo9a
|
UTSW |
9 |
59,895,283 (GRCm38) |
missense |
probably damaging |
1.00 |
R4197:Myo9a
|
UTSW |
9 |
59,894,866 (GRCm38) |
missense |
probably benign |
0.09 |
R4212:Myo9a
|
UTSW |
9 |
59,906,066 (GRCm38) |
nonsense |
probably null |
|
R4610:Myo9a
|
UTSW |
9 |
59,871,882 (GRCm38) |
missense |
probably benign |
|
R4616:Myo9a
|
UTSW |
9 |
59,821,649 (GRCm38) |
missense |
probably damaging |
1.00 |
R4621:Myo9a
|
UTSW |
9 |
59,871,072 (GRCm38) |
missense |
probably benign |
0.00 |
R4623:Myo9a
|
UTSW |
9 |
59,871,072 (GRCm38) |
missense |
probably benign |
0.00 |
R4632:Myo9a
|
UTSW |
9 |
59,869,664 (GRCm38) |
missense |
probably benign |
0.00 |
R4657:Myo9a
|
UTSW |
9 |
59,875,416 (GRCm38) |
critical splice donor site |
probably null |
|
R4892:Myo9a
|
UTSW |
9 |
59,824,242 (GRCm38) |
missense |
probably damaging |
0.98 |
R4897:Myo9a
|
UTSW |
9 |
59,896,517 (GRCm38) |
missense |
probably benign |
0.07 |
R4966:Myo9a
|
UTSW |
9 |
59,871,734 (GRCm38) |
missense |
probably benign |
0.00 |
R4993:Myo9a
|
UTSW |
9 |
59,861,472 (GRCm38) |
nonsense |
probably null |
|
R5160:Myo9a
|
UTSW |
9 |
59,871,802 (GRCm38) |
missense |
probably benign |
0.24 |
R5233:Myo9a
|
UTSW |
9 |
59,910,617 (GRCm38) |
missense |
probably damaging |
1.00 |
R5271:Myo9a
|
UTSW |
9 |
59,907,382 (GRCm38) |
missense |
probably damaging |
1.00 |
R5308:Myo9a
|
UTSW |
9 |
59,863,961 (GRCm38) |
missense |
probably damaging |
1.00 |
R5367:Myo9a
|
UTSW |
9 |
59,900,449 (GRCm38) |
missense |
probably damaging |
0.96 |
R5432:Myo9a
|
UTSW |
9 |
59,865,670 (GRCm38) |
missense |
possibly damaging |
0.94 |
R5459:Myo9a
|
UTSW |
9 |
59,884,520 (GRCm38) |
missense |
probably damaging |
0.98 |
R5511:Myo9a
|
UTSW |
9 |
59,780,212 (GRCm38) |
missense |
probably damaging |
1.00 |
R5568:Myo9a
|
UTSW |
9 |
59,874,628 (GRCm38) |
missense |
probably benign |
|
R5573:Myo9a
|
UTSW |
9 |
59,871,001 (GRCm38) |
missense |
probably benign |
|
R5589:Myo9a
|
UTSW |
9 |
59,895,244 (GRCm38) |
nonsense |
probably null |
|
R5607:Myo9a
|
UTSW |
9 |
59,863,944 (GRCm38) |
missense |
probably damaging |
1.00 |
R5633:Myo9a
|
UTSW |
9 |
59,868,184 (GRCm38) |
missense |
possibly damaging |
0.60 |
R5885:Myo9a
|
UTSW |
9 |
59,871,220 (GRCm38) |
missense |
probably benign |
|
R6024:Myo9a
|
UTSW |
9 |
59,855,388 (GRCm38) |
missense |
possibly damaging |
0.68 |
R6086:Myo9a
|
UTSW |
9 |
59,790,057 (GRCm38) |
nonsense |
probably null |
|
R6146:Myo9a
|
UTSW |
9 |
59,871,229 (GRCm38) |
missense |
probably benign |
0.01 |
R6194:Myo9a
|
UTSW |
9 |
59,869,750 (GRCm38) |
missense |
probably benign |
0.00 |
R6213:Myo9a
|
UTSW |
9 |
59,827,258 (GRCm38) |
missense |
probably damaging |
1.00 |
R6368:Myo9a
|
UTSW |
9 |
59,924,948 (GRCm38) |
missense |
probably benign |
0.01 |
R6550:Myo9a
|
UTSW |
9 |
59,868,199 (GRCm38) |
missense |
probably damaging |
1.00 |
R6612:Myo9a
|
UTSW |
9 |
59,827,196 (GRCm38) |
missense |
probably damaging |
1.00 |
R6665:Myo9a
|
UTSW |
9 |
59,871,872 (GRCm38) |
missense |
probably benign |
0.09 |
R6951:Myo9a
|
UTSW |
9 |
59,894,768 (GRCm38) |
missense |
probably damaging |
1.00 |
R7026:Myo9a
|
UTSW |
9 |
59,815,334 (GRCm38) |
missense |
probably damaging |
1.00 |
R7107:Myo9a
|
UTSW |
9 |
59,870,815 (GRCm38) |
missense |
probably benign |
0.44 |
R7310:Myo9a
|
UTSW |
9 |
59,871,153 (GRCm38) |
missense |
probably benign |
0.08 |
R7473:Myo9a
|
UTSW |
9 |
59,895,244 (GRCm38) |
missense |
probably benign |
0.31 |
R7723:Myo9a
|
UTSW |
9 |
59,779,858 (GRCm38) |
missense |
probably damaging |
1.00 |
R7823:Myo9a
|
UTSW |
9 |
59,811,950 (GRCm38) |
missense |
probably damaging |
1.00 |
R7824:Myo9a
|
UTSW |
9 |
59,860,109 (GRCm38) |
missense |
probably damaging |
1.00 |
R7965:Myo9a
|
UTSW |
9 |
59,788,438 (GRCm38) |
missense |
probably damaging |
1.00 |
R8031:Myo9a
|
UTSW |
9 |
59,780,091 (GRCm38) |
missense |
probably benign |
0.33 |
R8055:Myo9a
|
UTSW |
9 |
59,907,460 (GRCm38) |
missense |
probably damaging |
1.00 |
R8071:Myo9a
|
UTSW |
9 |
59,874,648 (GRCm38) |
missense |
probably benign |
|
R8250:Myo9a
|
UTSW |
9 |
59,860,109 (GRCm38) |
missense |
probably damaging |
1.00 |
R8260:Myo9a
|
UTSW |
9 |
59,910,678 (GRCm38) |
missense |
probably benign |
0.08 |
R8355:Myo9a
|
UTSW |
9 |
59,909,847 (GRCm38) |
missense |
probably damaging |
1.00 |
R8432:Myo9a
|
UTSW |
9 |
59,780,265 (GRCm38) |
missense |
probably damaging |
1.00 |
R8470:Myo9a
|
UTSW |
9 |
59,832,290 (GRCm38) |
missense |
probably damaging |
1.00 |
R8528:Myo9a
|
UTSW |
9 |
59,860,140 (GRCm38) |
missense |
probably damaging |
1.00 |
R8681:Myo9a
|
UTSW |
9 |
59,868,111 (GRCm38) |
missense |
probably benign |
0.16 |
R8690:Myo9a
|
UTSW |
9 |
59,875,374 (GRCm38) |
missense |
probably benign |
|
R8793:Myo9a
|
UTSW |
9 |
59,884,567 (GRCm38) |
missense |
probably benign |
0.03 |
R8812:Myo9a
|
UTSW |
9 |
59,779,747 (GRCm38) |
missense |
probably benign |
0.14 |
R9016:Myo9a
|
UTSW |
9 |
59,868,144 (GRCm38) |
nonsense |
probably null |
|
R9026:Myo9a
|
UTSW |
9 |
59,809,474 (GRCm38) |
missense |
probably damaging |
0.96 |
R9036:Myo9a
|
UTSW |
9 |
59,780,301 (GRCm38) |
nonsense |
probably null |
|
R9130:Myo9a
|
UTSW |
9 |
59,832,231 (GRCm38) |
missense |
probably damaging |
0.98 |
R9131:Myo9a
|
UTSW |
9 |
59,861,489 (GRCm38) |
missense |
probably damaging |
1.00 |
R9213:Myo9a
|
UTSW |
9 |
59,865,639 (GRCm38) |
missense |
probably benign |
0.04 |
R9498:Myo9a
|
UTSW |
9 |
59,827,183 (GRCm38) |
missense |
probably damaging |
1.00 |
R9575:Myo9a
|
UTSW |
9 |
59,905,907 (GRCm38) |
missense |
probably damaging |
1.00 |
R9651:Myo9a
|
UTSW |
9 |
59,871,481 (GRCm38) |
missense |
probably damaging |
0.96 |
R9672:Myo9a
|
UTSW |
9 |
59,780,049 (GRCm38) |
missense |
probably benign |
0.16 |
RF018:Myo9a
|
UTSW |
9 |
59,869,586 (GRCm38) |
missense |
probably benign |
0.00 |
RF019:Myo9a
|
UTSW |
9 |
59,921,772 (GRCm38) |
missense |
probably benign |
0.00 |
Z1176:Myo9a
|
UTSW |
9 |
59,895,259 (GRCm38) |
missense |
probably damaging |
1.00 |
|