Variant #0000549697 (NC_000013.10:g.103506670G>A, NM_001204425.1:c.1775G>A (BIVM-ERCC5))

Chromosome 13
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.103506670G>A
DNA change (hg38) g.102854320G>A
Published as ERCC5(NM_000123.3):c.413G>A (p.R138Q)
ISCN -
DB-ID BIVM_000003
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.413G>A r.(?) p.(Arg138Gln)
BIVM NM_001159596.1 -?/. - c.*14455G>A r.(=) p.(=)
BIVM-ERCC5 NM_001204425.1 -?/. - c.1775G>A r.(?) p.(Arg592Gln)


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