Variant #0000564852 (NC_000018.9:g.43531186C>T, NM_020964.2:c.1271G>A (EPG5))

Chromosome 18
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.43531186C>T
DNA change (hg38) g.45951220C>T
Published as EPG5(NM_020964.2):c.1271G>A (p.(Ser424Asn)), EPG5(NM_020964.3):c.1271G>A (p.S424N)
ISCN -
DB-ID EPG5_000100 See all 4 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) 0.01102 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EPG5 NM_020964.2 -/. - c.1271G>A r.(?) p.(Ser424Asn)


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