Variant #0000969859 (NC_000019.9:g.50755981A>T, NM_024729.3:c.1892A>T (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.50755981A>T
DNA change (hg38) -
Published as MYH14(NM_001145809.2):c.1916A>T (p.D639V)
ISCN -
DB-ID MYH14_000286
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYH14 NM_001145809.1 ?/. - c.1916A>T r.(?) p.(Asp639Val)
MYH14 NM_024729.3 ?/. - c.1892A>T r.(?) p.(Asp631Val)


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