Variant #0000044720 (NC_000011.9:g.118023525A>G, NM_001142348.1:c.-137T>C (SCN4B))

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.118023525A>G
DNA change (hg38) g.118152810A>G
Published as -
ISCN -
DB-ID SCN4B_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 2014-10-10 14:04:55 +02:00 (CEST)
Date last edited 2014-10-11 12:45:06 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCN4B NM_001142348.1 ?/. 1 c.-137T>C r.(=) p.(=)



Screenings

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