Variant #0000891714 (NC_000014.8:g.23883316G>T, NC_000014.8(NM_000257.2):c.5560-5C>A (MYH7))

Chromosome 14
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.23883316G>T
DNA change (hg38) -
Published as MYH7(NM_000257.2):c.5560-5C>A
ISCN -
DB-ID MYH6_000615 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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYH7 NM_000257.2 ?/. - c.5560-5C>A r.spl? p.?
MYH6 NM_002471.3 ?/. - c.-5901C>A r.(?) p.(=)


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