Variant #0000276247 (NC_000019.9:g.45864905C>T, NC_000019.9(NM_000400.3):c.1119-5G>A (ERCC2))

Chromosome 19
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.45864905C>T
DNA change (hg38) g.45361647C>T
Published as ERCC2(NM_000400.3):c.1119-5G>A, ERCC2(NM_000400.4):c.1119-5G>A
ISCN -
DB-ID ERCC2_000025 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) 0.00022 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 2025-07-08 13:22:38 +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.1119-5G>A r.spl? p.?
KLC3 NM_177417.2 -?/. - c.*10290C>T r.(=) p.(=)


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