Incidental Mutation 'R0126:Myo5c'
| ID |
21378 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Myo5c
|
| Ensembl Gene |
ENSMUSG00000033590 |
| Gene Name |
myosin VC |
| Synonyms |
9130003O20Rik |
| MMRRC Submission |
038411-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R0126 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
9 |
| Chromosomal Location |
75139302-75212733 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 75176807 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Histidine to Leucine
at position 584
(H584L)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000042229
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000036555]
[ENSMUST00000216788]
|
| AlphaFold |
E9Q1F5 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000036555
AA Change: H584L
PolyPhen 2
Score 0.045 (Sensitivity: 0.94; Specificity: 0.83)
|
| SMART Domains |
Protein: ENSMUSP00000042229
Gene: ENSMUSG00000033590
AA Change: H584L
| Domain | Start | End | E-Value | Type |
|---|
|
MYSc
|
61 |
754 |
N/A |
SMART |
|
IQ
|
755 |
777 |
1.11e-3 |
SMART |
|
IQ
|
778 |
800 |
1.39e0 |
SMART |
|
IQ
|
806 |
828 |
8.98e-4 |
SMART |
|
IQ
|
829 |
851 |
4.19e-4 |
SMART |
|
IQ
|
854 |
876 |
2.54e-3 |
SMART |
|
coiled coil region
|
1160 |
1185 |
N/A |
INTRINSIC |
|
coiled coil region
|
1207 |
1245 |
N/A |
INTRINSIC |
|
DIL
|
1574 |
1679 |
5.54e-45 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000216788
|
| Meta Mutation Damage Score |
0.0847 |
| Coding Region Coverage |
- 1x: 98.8%
- 3x: 97.6%
- 10x: 93.2%
- 20x: 81.8%
|
| Validation Efficiency |
98% (102/104) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 85 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca2 |
T |
C |
2: 25,333,742 (GRCm39) |
L1730P |
possibly damaging |
Het |
| Adam9 |
T |
C |
8: 25,460,753 (GRCm39) |
N577S |
probably damaging |
Het |
| Add1 |
T |
C |
5: 34,770,923 (GRCm39) |
Y316H |
probably benign |
Het |
| Agpat3 |
T |
C |
10: 78,113,890 (GRCm39) |
D266G |
probably null |
Het |
| Aldh3a2 |
C |
A |
11: 61,115,384 (GRCm39) |
Q524H |
probably benign |
Het |
| Alox12b |
A |
C |
11: 69,058,297 (GRCm39) |
S550R |
probably benign |
Het |
| Ano4 |
T |
A |
10: 88,788,154 (GRCm39) |
I753F |
possibly damaging |
Het |
| AW011738 |
T |
A |
4: 156,288,104 (GRCm39) |
|
probably benign |
Het |
| B4galt3 |
C |
T |
1: 171,103,738 (GRCm39) |
T103M |
probably damaging |
Het |
| Cabs1 |
C |
T |
5: 88,128,054 (GRCm39) |
T235I |
probably damaging |
Het |
| Casq2 |
A |
G |
3: 102,040,715 (GRCm39) |
H272R |
probably damaging |
Het |
| Ccdc180 |
T |
C |
4: 45,912,866 (GRCm39) |
|
probably null |
Het |
| Cdh12 |
A |
T |
15: 21,584,031 (GRCm39) |
M624L |
probably benign |
Het |
| Cdh5 |
A |
C |
8: 104,867,314 (GRCm39) |
|
probably null |
Het |
| Col7a1 |
A |
G |
9: 108,798,651 (GRCm39) |
|
probably benign |
Het |
| Cpne2 |
A |
T |
8: 95,281,561 (GRCm39) |
I199F |
probably damaging |
Het |
| Crebbp |
A |
T |
16: 3,901,927 (GRCm39) |
F2399L |
possibly damaging |
Het |
| Defb36 |
T |
C |
2: 152,454,499 (GRCm39) |
C53R |
probably damaging |
Het |
| Degs1 |
T |
C |
1: 182,107,257 (GRCm39) |
M1V |
probably null |
Het |
| Disp2 |
T |
A |
2: 118,620,819 (GRCm39) |
F517Y |
probably damaging |
Het |
| Dnah5 |
A |
G |
15: 28,246,465 (GRCm39) |
D601G |
probably benign |
Het |
| Dnpep |
G |
A |
1: 75,289,182 (GRCm39) |
Q310* |
probably null |
Het |
| Dsg1a |
A |
G |
18: 20,473,935 (GRCm39) |
T1003A |
probably benign |
Het |
| Fbrsl1 |
C |
G |
5: 110,543,906 (GRCm39) |
|
probably benign |
Het |
| Foxh1 |
A |
T |
15: 76,553,454 (GRCm39) |
L116H |
probably damaging |
Het |
| Gigyf2 |
G |
A |
1: 87,339,597 (GRCm39) |
|
probably benign |
Het |
| Golm2 |
T |
C |
2: 121,736,565 (GRCm39) |
|
probably benign |
Het |
| Gp1ba |
A |
T |
11: 70,531,859 (GRCm39) |
|
probably benign |
Het |
| Gucy1b1 |
A |
G |
3: 81,945,218 (GRCm39) |
|
probably benign |
Het |
| Gucy2g |
T |
G |
19: 55,229,598 (GRCm39) |
D24A |
probably benign |
Het |
| Hirip3 |
A |
G |
7: 126,462,614 (GRCm39) |
K190R |
probably damaging |
Het |
| Hmmr |
T |
C |
11: 40,596,781 (GRCm39) |
N717D |
probably damaging |
Het |
| Il12b |
A |
T |
11: 44,301,045 (GRCm39) |
Y187F |
probably damaging |
Het |
| Iqgap1 |
A |
G |
7: 80,388,070 (GRCm39) |
I859T |
probably benign |
Het |
| Jmjd1c |
T |
C |
10: 67,055,105 (GRCm39) |
L175P |
probably damaging |
Het |
| Klc2 |
T |
C |
19: 5,162,774 (GRCm39) |
M242V |
possibly damaging |
Het |
| Klf3 |
T |
C |
5: 64,979,446 (GRCm39) |
M96T |
probably benign |
Het |
| Lrrc66 |
G |
T |
5: 73,764,431 (GRCm39) |
H871N |
probably benign |
Het |
| Ltn1 |
A |
T |
16: 87,222,528 (GRCm39) |
D168E |
probably benign |
Het |
| Mak |
T |
C |
13: 41,186,072 (GRCm39) |
D532G |
probably damaging |
Het |
| Marchf6 |
A |
G |
15: 31,462,151 (GRCm39) |
M859T |
probably benign |
Het |
| Meak7 |
T |
C |
8: 120,489,089 (GRCm39) |
D398G |
possibly damaging |
Het |
| Mlxipl |
C |
A |
5: 135,161,177 (GRCm39) |
N365K |
probably damaging |
Het |
| Mplkip |
T |
C |
13: 17,870,337 (GRCm39) |
S90P |
possibly damaging |
Het |
| Myt1l |
A |
G |
12: 29,901,719 (GRCm39) |
T228A |
possibly damaging |
Het |
| Nxpe3 |
A |
T |
16: 55,686,592 (GRCm39) |
Y139N |
possibly damaging |
Het |
| Or2z8 |
C |
T |
8: 72,812,244 (GRCm39) |
T240M |
probably damaging |
Het |
| Or51f2 |
A |
G |
7: 102,526,347 (GRCm39) |
T7A |
probably benign |
Het |
| Or8k40 |
T |
A |
2: 86,584,981 (GRCm39) |
I34L |
probably damaging |
Het |
| Pak6 |
C |
T |
2: 118,520,813 (GRCm39) |
S268F |
possibly damaging |
Het |
| Parp10 |
G |
A |
15: 76,127,266 (GRCm39) |
A57V |
probably damaging |
Het |
| Pik3r3 |
T |
A |
4: 116,113,465 (GRCm39) |
D69E |
probably damaging |
Het |
| Polr2a |
T |
G |
11: 69,638,251 (GRCm39) |
K105T |
probably damaging |
Het |
| Prdm16 |
A |
T |
4: 154,413,295 (GRCm39) |
|
probably benign |
Het |
| Prepl |
G |
A |
17: 85,390,670 (GRCm39) |
T96I |
probably benign |
Het |
| Ret |
C |
T |
6: 118,142,956 (GRCm39) |
|
probably benign |
Het |
| Rgl3 |
A |
T |
9: 21,887,108 (GRCm39) |
D541E |
probably benign |
Het |
| Rpa1 |
A |
C |
11: 75,209,355 (GRCm39) |
Y143D |
probably benign |
Het |
| Rps16 |
T |
A |
7: 28,050,508 (GRCm39) |
L47Q |
probably damaging |
Het |
| Sbno2 |
A |
T |
10: 79,904,687 (GRCm39) |
|
probably null |
Het |
| Scube1 |
A |
T |
15: 83,505,264 (GRCm39) |
N385K |
probably damaging |
Het |
| Shank2 |
A |
G |
7: 143,585,092 (GRCm39) |
E31G |
probably damaging |
Het |
| Slc38a9 |
G |
T |
13: 112,865,791 (GRCm39) |
C496F |
possibly damaging |
Het |
| Snap47 |
A |
G |
11: 59,328,813 (GRCm39) |
V163A |
probably damaging |
Het |
| Sntg2 |
T |
C |
12: 30,251,260 (GRCm39) |
|
probably benign |
Het |
| Sp7 |
C |
A |
15: 102,266,895 (GRCm39) |
V322F |
probably damaging |
Het |
| Spic |
T |
C |
10: 88,511,924 (GRCm39) |
K111E |
probably damaging |
Het |
| Sqor |
T |
C |
2: 122,639,947 (GRCm39) |
|
probably benign |
Het |
| St6galnac1 |
T |
A |
11: 116,657,410 (GRCm39) |
M385L |
probably benign |
Het |
| Synpo2 |
A |
T |
3: 122,873,511 (GRCm39) |
S1211T |
possibly damaging |
Het |
| Sytl2 |
T |
A |
7: 90,045,797 (GRCm39) |
V638E |
probably damaging |
Het |
| Taar1 |
T |
A |
10: 23,796,445 (GRCm39) |
S48T |
probably benign |
Het |
| Tbx18 |
T |
A |
9: 87,611,706 (GRCm39) |
D108V |
possibly damaging |
Het |
| Tdh |
C |
T |
14: 63,735,042 (GRCm39) |
|
probably benign |
Het |
| Tlr9 |
T |
A |
9: 106,102,881 (GRCm39) |
L724Q |
probably benign |
Het |
| Tmem270 |
T |
A |
5: 134,931,642 (GRCm39) |
Y100F |
probably benign |
Het |
| Trim65 |
G |
C |
11: 116,015,430 (GRCm39) |
|
probably benign |
Het |
| Trrap |
A |
T |
5: 144,742,560 (GRCm39) |
K1393* |
probably null |
Het |
| Ttc13 |
A |
G |
8: 125,410,030 (GRCm39) |
V523A |
probably damaging |
Het |
| Utrn |
T |
A |
10: 12,587,219 (GRCm39) |
D939V |
probably benign |
Het |
| Vmn1r46 |
G |
T |
6: 89,953,935 (GRCm39) |
M261I |
probably benign |
Het |
| Vwa5a |
A |
G |
9: 38,649,103 (GRCm39) |
|
probably null |
Het |
| Zfp108 |
A |
T |
7: 23,960,149 (GRCm39) |
T247S |
probably benign |
Het |
| Zfp366 |
A |
T |
13: 99,365,129 (GRCm39) |
I97F |
probably benign |
Het |
| Zfp986 |
C |
T |
4: 145,625,513 (GRCm39) |
R58C |
probably benign |
Het |
|
| Other mutations in Myo5c |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00093:Myo5c
|
APN |
9 |
75,150,162 (GRCm39) |
splice site |
probably benign |
|
|
IGL00848:Myo5c
|
APN |
9 |
75,196,463 (GRCm39) |
missense |
probably benign |
|
|
IGL01503:Myo5c
|
APN |
9 |
75,170,324 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01735:Myo5c
|
APN |
9 |
75,208,720 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01866:Myo5c
|
APN |
9 |
75,176,864 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL01956:Myo5c
|
APN |
9 |
75,150,158 (GRCm39) |
splice site |
probably null |
|
|
IGL02127:Myo5c
|
APN |
9 |
75,208,184 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02268:Myo5c
|
APN |
9 |
75,153,519 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02272:Myo5c
|
APN |
9 |
75,173,442 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
IGL03052:Myo5c
|
APN |
9 |
75,159,798 (GRCm39) |
splice site |
probably benign |
|
|
IGL03179:Myo5c
|
APN |
9 |
75,163,148 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
IGL03224:Myo5c
|
APN |
9 |
75,185,525 (GRCm39) |
missense |
probably benign |
0.01 |
|
Marked
|
UTSW |
9 |
75,182,919 (GRCm39) |
critical splice donor site |
probably null |
|
|
pixie
|
UTSW |
9 |
75,193,860 (GRCm39) |
missense |
probably benign |
0.26 |
|
PIT4142001:Myo5c
|
UTSW |
9 |
75,191,230 (GRCm39) |
missense |
probably benign |
0.00 |
|
PIT4431001:Myo5c
|
UTSW |
9 |
75,159,853 (GRCm39) |
missense |
possibly damaging |
0.75 |
|
R0266:Myo5c
|
UTSW |
9 |
75,191,498 (GRCm39) |
splice site |
probably benign |
|
|
R0345:Myo5c
|
UTSW |
9 |
75,204,701 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0387:Myo5c
|
UTSW |
9 |
75,192,303 (GRCm39) |
splice site |
probably benign |
|
|
R0602:Myo5c
|
UTSW |
9 |
75,173,478 (GRCm39) |
splice site |
probably null |
|
|
R0675:Myo5c
|
UTSW |
9 |
75,185,571 (GRCm39) |
missense |
probably benign |
|
|
R0798:Myo5c
|
UTSW |
9 |
75,165,266 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0981:Myo5c
|
UTSW |
9 |
75,178,873 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1051:Myo5c
|
UTSW |
9 |
75,198,165 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1072:Myo5c
|
UTSW |
9 |
75,199,490 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1144:Myo5c
|
UTSW |
9 |
75,193,730 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1454:Myo5c
|
UTSW |
9 |
75,170,348 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R1476:Myo5c
|
UTSW |
9 |
75,183,221 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1484:Myo5c
|
UTSW |
9 |
75,208,092 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1586:Myo5c
|
UTSW |
9 |
75,174,313 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1616:Myo5c
|
UTSW |
9 |
75,203,299 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1635:Myo5c
|
UTSW |
9 |
75,184,357 (GRCm39) |
missense |
probably benign |
0.09 |
|
R1800:Myo5c
|
UTSW |
9 |
75,153,446 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1838:Myo5c
|
UTSW |
9 |
75,180,835 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1840:Myo5c
|
UTSW |
9 |
75,157,017 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1885:Myo5c
|
UTSW |
9 |
75,157,043 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1897:Myo5c
|
UTSW |
9 |
75,199,523 (GRCm39) |
missense |
probably benign |
0.20 |
|
R1898:Myo5c
|
UTSW |
9 |
75,204,908 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2029:Myo5c
|
UTSW |
9 |
75,196,337 (GRCm39) |
unclassified |
probably benign |
|
|
R2063:Myo5c
|
UTSW |
9 |
75,189,150 (GRCm39) |
missense |
probably benign |
0.19 |
|
R2230:Myo5c
|
UTSW |
9 |
75,180,888 (GRCm39) |
missense |
probably benign |
|
|
R2519:Myo5c
|
UTSW |
9 |
75,157,718 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2520:Myo5c
|
UTSW |
9 |
75,204,931 (GRCm39) |
nonsense |
probably null |
|
|
R3034:Myo5c
|
UTSW |
9 |
75,193,859 (GRCm39) |
missense |
probably benign |
0.44 |
|
R3117:Myo5c
|
UTSW |
9 |
75,173,476 (GRCm39) |
critical splice donor site |
probably null |
|
|
R3432:Myo5c
|
UTSW |
9 |
75,170,283 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3751:Myo5c
|
UTSW |
9 |
75,183,284 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4132:Myo5c
|
UTSW |
9 |
75,159,850 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4173:Myo5c
|
UTSW |
9 |
75,153,540 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4239:Myo5c
|
UTSW |
9 |
75,191,224 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4429:Myo5c
|
UTSW |
9 |
75,201,283 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4574:Myo5c
|
UTSW |
9 |
75,176,893 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4791:Myo5c
|
UTSW |
9 |
75,198,198 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4804:Myo5c
|
UTSW |
9 |
75,152,306 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4819:Myo5c
|
UTSW |
9 |
75,199,484 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R4881:Myo5c
|
UTSW |
9 |
75,191,434 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4900:Myo5c
|
UTSW |
9 |
75,180,825 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4964:Myo5c
|
UTSW |
9 |
75,204,791 (GRCm39) |
missense |
possibly damaging |
0.51 |
|
R4966:Myo5c
|
UTSW |
9 |
75,176,878 (GRCm39) |
missense |
probably benign |
0.03 |
|
R5057:Myo5c
|
UTSW |
9 |
75,208,155 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5347:Myo5c
|
UTSW |
9 |
75,202,487 (GRCm39) |
missense |
probably null |
1.00 |
|
R5399:Myo5c
|
UTSW |
9 |
75,195,356 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R5440:Myo5c
|
UTSW |
9 |
75,165,407 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R5569:Myo5c
|
UTSW |
9 |
75,180,792 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5600:Myo5c
|
UTSW |
9 |
75,196,436 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5606:Myo5c
|
UTSW |
9 |
75,182,790 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5704:Myo5c
|
UTSW |
9 |
75,180,185 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5798:Myo5c
|
UTSW |
9 |
75,191,480 (GRCm39) |
missense |
probably benign |
0.04 |
|
R5865:Myo5c
|
UTSW |
9 |
75,204,770 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R6034:Myo5c
|
UTSW |
9 |
75,163,187 (GRCm39) |
missense |
probably benign |
0.05 |
|
R6034:Myo5c
|
UTSW |
9 |
75,163,187 (GRCm39) |
missense |
probably benign |
0.05 |
|
R6143:Myo5c
|
UTSW |
9 |
75,157,091 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6242:Myo5c
|
UTSW |
9 |
75,180,893 (GRCm39) |
missense |
probably benign |
|
|
R6253:Myo5c
|
UTSW |
9 |
75,152,319 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6264:Myo5c
|
UTSW |
9 |
75,182,836 (GRCm39) |
missense |
probably benign |
|
|
R6307:Myo5c
|
UTSW |
9 |
75,180,198 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R6358:Myo5c
|
UTSW |
9 |
75,203,294 (GRCm39) |
missense |
possibly damaging |
0.53 |
|
R6450:Myo5c
|
UTSW |
9 |
75,193,860 (GRCm39) |
missense |
probably benign |
0.26 |
|
R6598:Myo5c
|
UTSW |
9 |
75,153,516 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6618:Myo5c
|
UTSW |
9 |
75,182,919 (GRCm39) |
critical splice donor site |
probably null |
|
|
R6774:Myo5c
|
UTSW |
9 |
75,196,468 (GRCm39) |
missense |
probably benign |
0.05 |
|
R6865:Myo5c
|
UTSW |
9 |
75,176,878 (GRCm39) |
missense |
probably benign |
0.03 |
|
R6996:Myo5c
|
UTSW |
9 |
75,157,746 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7023:Myo5c
|
UTSW |
9 |
75,208,738 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7123:Myo5c
|
UTSW |
9 |
75,196,505 (GRCm39) |
missense |
probably benign |
|
|
R7250:Myo5c
|
UTSW |
9 |
75,169,497 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7316:Myo5c
|
UTSW |
9 |
75,176,920 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7340:Myo5c
|
UTSW |
9 |
75,196,423 (GRCm39) |
missense |
probably benign |
|
|
R7382:Myo5c
|
UTSW |
9 |
75,211,332 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7426:Myo5c
|
UTSW |
9 |
75,158,809 (GRCm39) |
splice site |
probably null |
|
|
R7788:Myo5c
|
UTSW |
9 |
75,186,627 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7956:Myo5c
|
UTSW |
9 |
75,159,845 (GRCm39) |
missense |
probably benign |
|
|
R8082:Myo5c
|
UTSW |
9 |
75,182,793 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
R8290:Myo5c
|
UTSW |
9 |
75,196,178 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8406:Myo5c
|
UTSW |
9 |
75,182,823 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8481:Myo5c
|
UTSW |
9 |
75,208,726 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8489:Myo5c
|
UTSW |
9 |
75,180,128 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R8505:Myo5c
|
UTSW |
9 |
75,153,423 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8685:Myo5c
|
UTSW |
9 |
75,192,229 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R8806:Myo5c
|
UTSW |
9 |
75,150,054 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8871:Myo5c
|
UTSW |
9 |
75,185,585 (GRCm39) |
missense |
probably benign |
0.10 |
|
R9323:Myo5c
|
UTSW |
9 |
75,153,531 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9484:Myo5c
|
UTSW |
9 |
75,204,770 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9639:Myo5c
|
UTSW |
9 |
75,165,477 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1088:Myo5c
|
UTSW |
9 |
75,152,341 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1177:Myo5c
|
UTSW |
9 |
75,153,537 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- TGGACTCTGAAGCTGAGCCAAAGG -3'
(R):5'- GGCACTGGGATGTGCTAAACTGAAG -3'
Sequencing Primer
(F):5'- TCTGCCAGATGGAGCAGTG -3'
(R):5'- GTGAccacctcccacctc -3'
|
| Posted On |
2013-04-11 |
Incidental Mutation