Variant #0000617513 (NC_000019.9:g.35524461G>A, NM_199037.3:c.266G>A (SCN1B))

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.35524461G>A
DNA change (hg38) g.35033557G>A
Published as SCN1B(NM_001037.5):c.266G>A (p.R89H)
ISCN -
DB-ID SCN1B_000062 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) 3.0E-5 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 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCN1B NM_001037.4 ?/. - c.266G>A r.(?) p.(Arg89His)
SCN1B NM_199037.3 ?/. - c.266G>A r.(?) p.(Arg89His)


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