Variant #0000931089 (NC_000019.9:g.50747495C>T, NC_000019.9(NM_024729.3):c.1091-4C>T (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.50747495C>T
DNA change (hg38) -
Published as MYH14(NM_024729.4):c.1091-4C>T
ISCN -
DB-ID MYH14_000175 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) 0.00046 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 2023-07-07 10:10:56 +02:00 (CEST)
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.1115-4C>T r.spl? p.?
MYH14 NM_024729.3 -?/. - c.1091-4C>T r.spl? p.?


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