Variant #0000276271 (NC_000019.9:g.45867676C>A, NC_000019.9(NM_000400.3):c.718+6G>T (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.45867676C>A
DNA change (hg38) g.45364418C>A
Published as ERCC2(NM_000400.3):c.718+6G>T, ERCC2(NM_000400.4):c.718+6G>T
ISCN -
DB-ID ERCC2_000030 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) 0.00808 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 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ERCC2 NM_000400.3 -/. - c.718+6G>T r.(=) p.(=)
KLC3 NM_177417.2 -/. - c.*13061C>A r.(=) p.(=)


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