Variant #0000829757 (NC_000008.10:g.57080958del, NC_000008.10(NM_002655.2):c.-117-5del (PLAG1))

Chromosome 8
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.57080958del
DNA change (hg38) -
Published as -
ISCN -
DB-ID PLAG1_000003
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1023307529
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2021-12-15 16:14:01 +01:00 (CET)
Date last edited 2022-09-26 12:22:42 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PLAG1 NM_002655.2 ?/. - c.-117-5del r.(?) p.(?)


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