Variant #0000344399 (NC_000012.11:g.6458497A>G, NM_001038.5:c.1435T>C (SCNN1A))

Chromosome 12
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.6458497A>G
DNA change (hg38) g.6349331A>G
Published as SCNN1A(NM_001038.6):c.1435T>C (p.C479R)
ISCN -
DB-ID SCNN1A_000020 See all 2 reported entries
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) 0.0001 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCNN1A NM_001038.5 ?/. - c.1435T>C r.(?) p.(Cys479Arg)
LTBR NM_001270987.1 ?/. - c.-26225A>G r.(?) p.(=)


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