Variant #0000562915 (NC_000017.10:g.7097731A>T, NM_000018.3:c.-25573A>T (ACADVL))

Chromosome 17
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.7097731A>T
DNA change (hg38) g.7194412A>T
Published as DLG4(NM_001365.4):c.1514T>A (p.V505D)
ISCN -
DB-ID DLG4_000021
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-11-11 16:12:31 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACADVL NM_000018.3 ?/. - c.-25573A>T r.(?) p.(=)
DLG4 NM_001365.3 ?/. - c.1514T>A r.(?) p.(Val505Asp)


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