Variant #0000548960 (NC_000012.11:g.6458350A>G, NM_001038.5:c.1477T>C (SCNN1A))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.6458350A>G
DNA change (hg38) g.6349184A>G
Published as SCNN1A(NM_001159576.2):c.1654T>C (p.W552R)
ISCN -
DB-ID SCNN1A_000013 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) 0.01936 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCNN1A NM_001038.5 -?/. - c.1477T>C r.(?) p.(Trp493Arg)
LTBR NM_001270987.1 -?/. - c.-26372A>G r.(?) p.(=)


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