Variant #0000813830 (NC_000006.11:g.76542642G>A, NM_004999.3:c.475G>A (MYO6))

Chromosome 6
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.76542642G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID MYO6_000130
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs201507590
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00046 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2021-10-07 18:25:01 +02:00 (CEST)
Date last edited 2022-09-26 12:22:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
MYO6 NM_004999.3 ?/. - c.475G>A r.(?) p.(Glu159Lys) -


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