Variant #0000247649 (NC_000019.9:g.35523494A>C, NM_199037.3:c.103A>C (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.35523494A>C
DNA change (hg38) g.35032590A>C
Published as SCN1B(NM_001037.5):c.103A>C (p.T35P)
ISCN -
DB-ID SCN1B_000027
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 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 2018-01-15 20:58:59 +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.103A>C r.(?) p.(Thr35Pro)
SCN1B NM_199037.3 ?/. - c.103A>C r.(?) p.(Thr35Pro)


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