Variant #0001068028 (NC_000019.9:g.50735285G>C, NM_001145809.1:c.1072G>C (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.50735285G>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID MYH14_000303
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs901652663
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-02-02 12:20:02 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYH14 NM_001145809.1 ?/. - c.1072G>C r.(?) p.(Glu358Gln)


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