Variant #0000839365 (NC_000019.9:g.50753937G>A, NM_001145809.1:c.1822G>A (MYH14))

Chromosome 19
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.50753937G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID MYH14_000254
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs576014205
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2022-02-07 16:46:01 +01:00 (CET)
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     
MYH14 NM_001145809.1 ?/. - c.1822G>A r.(?) p.(Ala608Thr)


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