Variant #0000913933 (NC_000012.11:g.6457045C>A, NM_001038.5:c.2004G>T (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.6457045C>A
DNA change (hg38) -
Published as SCNN1A(NM_001038.6):c.2004G>T (p.G668=)
ISCN -
DB-ID LTBR_000010
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) 0.00026 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-01-11 15:44:22 +01:00 (CET)
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.2004G>T r.(?) p.(Gly668=)
LTBR NM_001270987.1 -?/. - c.-27677C>A r.(?) p.(=)


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