Variant #0000692455 (NC_000017.10:g.7126549T>C, NM_000018.3:c.1175T>C (ACADVL))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.7126549T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID DLG4_000050
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACADVL NM_000018.3 +?/. - c.1175T>C r.(?) p.(Val392Ala)
DLG4 NM_001365.3 +?/. - c.-4381A>G r.(?) p.(=)
DVL2 NM_004422.2 +?/. - c.*2635A>G r.(=) p.(=)


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