Variant #0000618079 (NC_000020.10:g.33581222G>A, NM_020884.3:c.2519G>A (MYH7B))

Chromosome 20
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.33581222G>A
DNA change (hg38) g.34993419G>A
Published as MYH7B(NM_020884.4):c.2519G>A (p.R840Q)
ISCN -
DB-ID MYH7B_000055 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) 0.0002 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2021-02-08 18:36:18 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRPC4AP NM_015638.2 ?/. - c.*9727C>T r.(=) p.(=)
MYH7B NM_020884.3 ?/. - c.2519G>A r.(?) p.(Arg840Gln)


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