Variant #0000568104 (NC_000019.9:g.50730169A>G, NM_024729.3:c.796A>G (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.50730169A>G
DNA change (hg38) g.50226912A>G
Published as MYH14(NM_001145809.1):c.820A>G (p.I274V), MYH14(NM_001145809.2):c.820A>G (p.I274V)
ISCN -
DB-ID MYH14_000098 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) 0.00043 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +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.820A>G r.(?) p.(Ile274Val)
MYH14 NM_024729.3 ?/. - c.796A>G r.(?) p.(Ile266Val)


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