Variant #0000249917 (NC_000013.10:g.103513944A>G, NM_001204425.1:c.2122A>G (BIVM-ERCC5))

Chromosome 13
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.103513944A>G
DNA change (hg38) g.102861594A>G
Published as ERCC5(NM_000123.3):c.760A>G (p.M254V), ERCC5(NM_000123.4):c.760A>G (p.M254V)
ISCN -
DB-ID ERCC5_000016 See all 4 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) 0.02984 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ERCC5 NM_000123.2 -/. - c.760A>G r.(?) p.(Met254Val)
BIVM NM_001159596.1 -/. - c.*21729A>G r.(=) p.(=)
BIVM-ERCC5 NM_001204425.1 -/. - c.2122A>G r.(?) p.(Met708Val)


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