Variant #0000403960 (NC_000004.11:g.39978005A>G, NC_000004.11(NM_001100399.1):c.138+55T>C (PDS5A))

Chromosome 4
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.39978005A>G
DNA change (hg38) g.39976385A>G
Published as 18+55T>C
ISCN -
DB-ID PDS5A_000017
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs35426579
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-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2010-04-09 14:18:57 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDS5A NM_001100399.1 -/. 2i c.138+55T>C r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.