Variant #0000982771 (NC_000017.10:g.7127641C>T, NM_000018.3:c.1534C>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.7127641C>T
DNA change (hg38) -
Published as ACADVL(NM_000018.4):c.1534C>T (p.(Arg512Trp)), ACADVL(NM_001270448.1):c.1306C>T (p.R436W)
ISCN -
DB-ID DLG4_000059 See all 2 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) 5.0E-5 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 2024-04-19 20:27:30 +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     
ACADVL NM_000018.3 ?/. - c.1534C>T r.(?) p.(Arg512Trp)
DLG4 NM_001365.3 ?/. - c.-5473G>A r.(?) p.(=)
DVL2 NM_004422.2 ?/. - c.*1543G>A r.(=) p.(=)


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