Variant #0000569463 (NC_000020.10:g.33539613G>A, NM_020884.3:c.-4408G>A (MYH7B))

Chromosome 20
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.33539613G>A
DNA change (hg38) g.34951810G>A
Published as GSS(NM_001322495.1):c.43C>T (p.L15=)
ISCN -
DB-ID MYH7B_000023
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-16 16:42:47 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GSS NM_000178.2 -?/. - c.43C>T r.(?) p.(Leu15=)
TRPC4AP NM_015638.2 -?/. - c.*51336C>T r.(=) p.(=)
MYH7B NM_020884.3 -?/. - c.-4408G>A r.(?) p.(=)


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