Variant #0000044719 (NC_000019.9:g.35524817_35524818del, NM_199037.3:c.622_623del (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.35524817_35524818del
DNA change (hg38) g.35033913_35033914del
Published as delCT
ISCN -
DB-ID SCN1B_000003 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Uschi Peeters
Database submission license No license selected
Created by Uschi Peeters
Date created 2014-10-10 14:01:08 +02:00 (CEST)
Date last edited 2014-10-11 13:06:24 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCN1B NM_199037.3 ?/. 3 c.622_623del r.(?) p.(Leu208Valfs*99)



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