Variant #0000150103 (NC_000007.13:g.75583468_75583470del, NM_000941.2:c.158_160del (POR))

Chromosome 7
Allele Parent #1
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.75583468_75583470del
DNA change (hg38) g.75954150_75954152del
Published as E53del
ISCN -
DB-ID POR_000074
Variant remarks -
Reference PubMed: Huang 2008
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2016-12-15 19:35:13 +01:00 (CET)
Date last edited 2020-06-23 09:46:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
POR NM_000941.2 ?/. 2 c.158_160del - r.(?) p.(Glu53del)



Screenings

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