Variant #0001002874 (NC_000017.10:g.10314233A>C, NM_002472.2:c.1448T>G (MYH8))

Chromosome 17
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.10314233A>C
DNA change (hg38) -
Published as MYH8(NM_002472.2):c.1448T>G (p.(Phe483Cys)), MYH8(NM_002472.3):c.1448T>G (p.F483C)
ISCN -
DB-ID MYH8_000062 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited 2025-07-08 13:22:38 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYH8 NM_002472.2 ?/. - c.1448T>G r.(?) p.(Phe483Cys)


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