Variant #0000562703 (NC_000017.10:g.62049790A>G, SCN4A(NM_000334.4):c.314T>C)

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.62049790A>G
DNA change (hg38) g.63972430A>G
Published as SCN4A(NM_000334.4):c.314T>C (p.(Phe105Ser))
ISCN -
DB-ID SCN4A_000216
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner VKGL-NL_Leiden
Database submission license No license selected
Created by VKGL-NL_Leiden
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCN4A NM_000334.4 ?/. - c.314T>C r.(?) p.(Phe105Ser)