Variant #0000624147 (NC_000020.10:g.33517253G>A, NM_020884.3:c.-26768G>A (MYH7B))

Chromosome 20
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.33517253G>A
DNA change (hg38) g.34929450G>A
Published as GSS(NM_001322495.1):c.1252C>T (p.R418*)
ISCN -
DB-ID MYH7B_000038
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) 2.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2020-07-16 16:41:06 +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.1252C>T r.(?) p.(Arg418Ter)
ACSS2 NM_018677.3 +?/. - c.*2236G>A r.(=) p.(=)
MYH7B NM_020884.3 +?/. - c.-26768G>A r.(?) p.(=)


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