Variant #0001040983 (NC_000016.9:g.2367764T>A, NM_001089.2:c.875A>T (ABCA3))

Chromosome 16
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.2367764T>A
DNA change (hg38) -
Published as ABCA3(NM_001089.2):c.875A>T (p.E292V), ABCA3(NM_001089.3):c.875A>T (p.(Glu292Val), p.E292V)
ISCN -
DB-ID ABCA3_000020 See all 4 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) 0.0023 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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     
ABCA3 NM_001089.2 +/. - c.875A>T r.(?) p.(Glu292Val)


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