Variant #0000853503 (NC_000012.11:g.6463975T>G, NM_001038.5:c.1183A>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.6463975T>G
DNA change (hg38) -
Published as SCNN1A(NM_001159576.1):c.1360A>C (p.T454P)
ISCN -
DB-ID LTBR_000009
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:40:45 +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.1183A>C r.(?) p.(Thr395Pro)
LTBR NM_001270987.1 ?/. - c.-20747T>G r.(?) p.(=)


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