Variant #0000967041 (NC_000012.11:g.6465059G>A, NC_000012.11(NM_001038.5):c.876-13C>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.6465059G>A
DNA change (hg38) -
Published as SCNN1A(NM_001038.6):c.876-13C>T
ISCN -
DB-ID LTBR_000012
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) 0.00036 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 2024-02-26 20:06:56 +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.876-13C>T r.(=) p.(=)
LTBR NM_001270987.1 -?/. - c.-19663G>A r.(?) p.(=)


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