Variant #0000254527 (NC_000019.9:g.50730175A>G, NM_024729.3:c.802A>G (MYH14))

Chromosome 19
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.50730175A>G
DNA change (hg38) g.50226918A>G
Published as MYH14(NM_001145809.1):c.826A>G (p.I276V)
ISCN -
DB-ID MYH14_000023
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) 0.00103 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYH14 NM_001145809.1 -?/. - c.826A>G r.(?) p.(Ile276Val)
MYH14 NM_024729.3 -?/. - c.802A>G r.(?) p.(Ile268Val)


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