Variant #0000255067 (NC_000019.9:g.50728907A>G, NM_024729.3:c.759A>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.50728907A>G
DNA change (hg38) g.50225650A>G
Published as MYH14(NM_001145809.1):c.783A>G (p.T261=)
ISCN -
DB-ID MYH14_000021
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) 1.0E-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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-16 11:05:35 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYH14 NM_001145809.1 -?/. - c.783A>G r.(?) p.(Thr261=)
MYH14 NM_024729.3 -?/. - c.759A>G r.(?) p.(Thr253=)


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