Variant #0000805907 (NC_000012.11:g.6458378del, NM_001038.5:c.1449del (SCNN1A))

Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.6458378del
DNA change (hg38) -
Published as SCNN1A(NM_001159576.2):c.1626delC (p.Y543Tfs*13)
ISCN -
DB-ID SCNN1A_000035 See all 6 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) 0.00013 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCNN1A NM_001038.5 +/. - c.1449del r.(?) p.(Tyr484ThrfsTer13)
LTBR NM_001270987.1 +/. - c.-26344del r.(?) p.(=)


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