Variant #0000851255 (NC_000006.11:g.53140059T>G, NM_021814.4:c.325A>C (ELOVL5))

Chromosome 6
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.53140059T>G
DNA change (hg38) -
Published as ELOVL5(NM_001301856.1):c.325A>C (p.I109L), ELOVL5(NM_001301856.2):c.325A>C (p.I109L), ELOVL5(NM_021814.5):c.325A>C (p.I109L)
ISCN -
DB-ID ELOVL5_000013 See all 3 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) 2.0E-5 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ELOVL5 NM_021814.4 ?/. - c.325A>C r.(?) p.(Ile109Leu)


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