Variant #0000894234 (NC_000017.10:g.7125284C>T, NM_000018.3:c.636C>T (ACADVL))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.7125284C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID DVL2_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) 0.00137 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACADVL NM_000018.3 -?/. - c.636C>T r.(?) p.(Ala212=)
DLG4 NM_001365.3 -?/. - c.-3116G>A r.(?) p.(=)
DVL2 NM_004422.2 -?/. - c.*3900G>A r.(=) p.(=)


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