Variant #0000301793 (NC_000019.9:g.35524607G>A, NM_199037.3:c.412G>A (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.35524607G>A
DNA change (hg38) g.35033703G>A
Published as SCN1B(NM_001037.4):c.412G>A (p.(Val138Ile)), SCN1B(NM_001037.5):c.412G>A (p.V138I)
ISCN -
DB-ID SCN1B_000035 See all 4 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) 0.01053 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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.412G>A r.(?) p.(Val138Ile)
SCN1B NM_199037.3 -?/. - c.412G>A r.(?) p.(Val138Ile)


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