Variant #0000267865 (NC_000019.9:g.45868309T>G, NM_000400.3:c.468A>C (ERCC2))

Chromosome 19
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.45868309T>G
DNA change (hg38) g.45365051T>G
Published as ERCC2(NM_000400.3):c.468A>C (p.R156=), ERCC2(NM_000400.4):c.468A>C (p.R156=)
ISCN -
DB-ID ERCC2_000037 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) 0.57953 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ERCC2 NM_000400.3 -/. - c.468A>C r.(?) p.(Arg156=)
KLC3 NM_177417.2 -/. - c.*13694T>G r.(=) p.(=)


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