Variant #0000623971 (NC_000019.9:g.35523532C>T, NM_199037.3:c.141C>T (SCN1B))

Chromosome 19
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.35523532C>T
DNA change (hg38) g.35032628C>T
Published as SCN1B(NM_199037.4):c.141C>T (p.S47=)
ISCN -
DB-ID SCN1B_000070
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 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2020-07-15 16:49:55 +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.141C>T r.(?) p.(Ser47=)
SCN1B NM_199037.3 -?/. - c.141C>T r.(?) p.(Ser47=)


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