Variant #0000567731 (NC_000019.9:g.45868291T>G, NC_000019.9(NM_000400.3):c.477+9A>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.45868291T>G
DNA change (hg38) g.45365033T>G
Published as ERCC2(NM_000400.3):c.477+9A>C, ERCC2(NM_000400.4):c.477+9A>C
ISCN -
DB-ID ERCC2_000075 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) 0.02479 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 2019-07-18 18:22:55 +02:00 (CEST)
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.477+9A>C r.(=) p.(=)
KLC3 NM_177417.2 -/. - c.*13676T>G r.(=) p.(=)


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