Variant #0000608531 (NC_000003.11:g.38105330A>G, NM_001607.3:c.*59208T>C (ACAA1))

Chromosome 3
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.38105330A>G
DNA change (hg38) g.38063839A>G
Published as DLEC1(NM_001321153.1):c.1095-2A>G
ISCN -
DB-ID ACAA1_000006
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 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-06-12 16:28:34 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACAA1 NM_001607.3 ?/. - c.*59208T>C r.(=) p.(=)
DLEC1 NM_007337.2 ?/. - c.1095-2A>G r.spl? p.?


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