Variant #0000519203 (NC_000003.11:g.38156497G>A, NM_001607.3:c.*8041C>T (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.38156497G>A
DNA change (hg38) g.38115006G>A
Published as DLEC1(NM_001321153.1):c.3818G>A (p.G1273E)
ISCN -
DB-ID ACAA1_000001
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 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACAA1 NM_001607.3 ?/. - c.*8041C>T r.(=) p.(=)
DLEC1 NM_007337.2 ?/. - c.3809G>A r.(?) p.(Gly1270Glu)


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