Variant #0000044718 (NC_000011.9:g.123513298G>T, NM_018400.3:c.301C>A (SCN3B))

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.123513298G>T
DNA change (hg38) g.123642590G>T
Published as -
ISCN -
DB-ID SCN3B_000001 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) 1.0E-5 View details
Owner Uschi Peeters
Database submission license No license selected
Created by Uschi Peeters
Date created 2014-10-10 13:53:32 +02:00 (CEST)
Date last edited 2014-10-11 12:48:22 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCN3B NM_018400.3 ?/. 3 c.301C>A r.(?) p.(Gln101Lys)



Screenings

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