Variant #0000808991 (NC_000019.9:g.50756015G>A, NC_000019.9(NM_024729.3):c.1921+5G>A (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.50756015G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID MYH14_000246
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYH14 NM_001145809.1 ?/. - c.1945+5G>A r.spl? p.?
MYH14 NM_024729.3 ?/. - c.1921+5G>A r.spl? p.?


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