Variant #0000276307 (NC_000013.10:g.103513972G>A, NM_001204425.1:c.2150G>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.103513972G>A
DNA change (hg38) g.102861622G>A
Published as ERCC5(NM_000123.3):c.788G>A (p.R263Q)
ISCN -
DB-ID ERCC5_000018
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) 0.00058 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ERCC5 NM_000123.2 -?/. - c.788G>A r.(?) p.(Arg263Gln)
BIVM NM_001159596.1 -?/. - c.*21757G>A r.(=) p.(=)
BIVM-ERCC5 NM_001204425.1 -?/. - c.2150G>A r.(?) p.(Arg717Gln)


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