Variant #0000235480 (NC_000003.11:g.38593004G>A, NM_198056.2:c.4859C>T (SCN5A))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.38593004G>A
DNA change (hg38) g.38551513G>A
Published as -
ISCN -
DB-ID SCN5A_000437 See all 6 reported entries
Variant remarks expression cloning did not show significant functional effects
Reference PubMed: Shirai 2002
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2017-12-06 13:50:25 +01:00 (CET)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCN5A NM_198056.2 -?/. 28 c.4859C>T r.(?) p.Thr1620Met


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