Variant #0000567698 (NC_000019.9:g.45855507G>C, NM_000400.3:c.2150C>G (ERCC2))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.45855507G>C
DNA change (hg38) g.45352249G>C
Published as ERCC2(NM_000400.3):c.2150C>G (p.A717G), ERCC2(NM_000400.4):c.2150C>G (p.(Ala717Gly), p.A717G)
ISCN -
DB-ID ERCC2_000050 See all 7 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) 0.00032 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +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.2150C>G r.(?) p.(Ala717Gly)
KLC3 NM_177417.2 +?/. - c.*892G>C r.(=) p.(=)


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