Variant #0000549696 (NC_000013.10:g.103504549C>T, NM_001204425.1:c.1532C>T (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.103504549C>T
DNA change (hg38) g.102852199C>T
Published as ERCC5(NM_000123.3):c.170C>T (p.T57I)
ISCN -
DB-ID BIVM_000002
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 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ERCC5 NM_000123.2 ?/. - c.170C>T r.(?) p.(Thr57Ile)
BIVM NM_001159596.1 ?/. - c.*12334C>T r.(=) p.(=)
BIVM-ERCC5 NM_001204425.1 ?/. - c.1532C>T r.(?) p.(Thr511Ile)


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