Variant #0000301779 (NC_000019.9:g.35521684C>G, NM_199037.3:c.-41C>G (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.35521684C>G
DNA change (hg38) g.35030780C>G
Published as SCN1B(NM_001037.5):c.-41C>G
ISCN -
DB-ID SCN1B_000024
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_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 2021-09-17 14:40:49 +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.-41C>G r.(?) p.(=)
GRAMD1A NM_020895.3 ?/. - c.*4639C>G r.(=) p.(=)
SCN1B NM_199037.3 ?/. - c.-41C>G r.(?) p.(=)


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