Variant #0000044892 (NC_000011.9:g.118047358G>A, NM_004588.4:c.-212C>T (SCN2B))

Chromosome 11
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.118047358G>A
DNA change (hg38) g.118176643G>A
Published as -
ISCN -
DB-ID SCN2B_000002 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 2014-10-17 10:31:24 +02:00 (CEST)
Date last edited 2014-10-31 19:24:17 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCN2B NM_004588.4 ?/. _1 c.-212C>T r.(=) p.(=)



Screenings

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