Variant #0000551872 (NC_000014.8:g.23868065T>G, NM_002471.3:c.1763A>C (MYH6))

Chromosome 14
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.23868065T>G
DNA change (hg38) g.23398856T>G
Published as MYH6(NM_002471.3):c.1763A>C (p.D588A, p.(Asp588Ala)), MYH6(NM_002471.4):c.1763A>C (p.D588A)
ISCN -
DB-ID MYH6_000008 See all 8 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) 0.00181 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYH6 NM_002471.3 -?/. - c.1763A>C r.(?) p.(Asp588Ala)


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