Variant #0000624057 (NC_000019.9:g.50728876C>A, NM_024729.3:c.728C>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.50728876C>A
DNA change (hg38) g.50225619C>A
Published as MYH14(NM_001145809.1):c.752C>A (p.P251H), MYH14(NM_001145809.2):c.752C>A (p.P251H)
ISCN -
DB-ID MYH14_000020 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYH14 NM_001145809.1 ?/. - c.752C>A r.(?) p.(Pro251His)
MYH14 NM_024729.3 ?/. - c.728C>A r.(?) p.(Pro243His)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.