Variant #0000681367 (NC_000019.9:g.35524460C>T, NM_199037.3:c.265C>T (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.35524460C>T
DNA change (hg38) -
Published as SCN1B(NM_199037.5):c.265C>T (p.R89C)
ISCN -
DB-ID SCN1B_000083 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) 1.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCN1B NM_001037.4 ?/. - c.265C>T r.(?) p.(Arg89Cys)
SCN1B NM_199037.3 ?/. - c.265C>T r.(?) p.(Arg89Cys)


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