Variant #0001000403 (NC_000013.10:g.103510688C>G, NM_001204425.1:c.1954C>G (BIVM-ERCC5))

Chromosome 13
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.103510688C>G
DNA change (hg38) -
Published as ERCC5(NM_000123.3):c.592C>G (p.P198A), ERCC5(NM_000123.4):c.592C>G (p.P198A)
ISCN -
DB-ID BIVM_000016 See all 2 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) 0.00022 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ERCC5 NM_000123.2 ?/. - c.592C>G r.(?) p.(Pro198Ala)
BIVM NM_001159596.1 ?/. - c.*18473C>G r.(=) p.(=)
BIVM-ERCC5 NM_001204425.1 ?/. - c.1954C>G r.(?) p.(Pro652Ala)


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