Variant #0000053055 (NC_000017.10:g.62019335A>G, NM_000334.4:c.4307T>C (SCN4A))

Chromosome 17
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.62019335A>G
DNA change (hg38) g.63941975A>G
Published as -
ISCN -
DB-ID SCN4A_000067 See all 5 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 2015-01-23 16:13:29 +01:00 (CET)
Date last edited 2015-01-23 22:01:14 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCN4A NM_000334.4 ?/. 24 c.4307T>C r.(?) p.(Leu1436Pro)



Screenings

Stop! No screenings found!


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.