Variant #0001000284 (NC_000012.11:g.6458565C>T, NM_001038.5:c.1367G>A (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.6458565C>T
DNA change (hg38) -
Published as SCNN1A(NM_001038.6):c.1367G>A (p.C456Y)
ISCN -
DB-ID LTBR_000013
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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCNN1A NM_001038.5 ?/. - c.1367G>A r.(?) p.(Cys456Tyr)
LTBR NM_001270987.1 ?/. - c.-26157C>T r.(?) p.(=)


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