Variant #0000276274 (NC_000002.11:g.128051290_128051292del, NM_000122.1:c.36_38del (ERCC3))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.128051290_128051292del
DNA change (hg38) g.127293714_127293716del
Published as ERCC3(NM_000122.1):c.36_38delGAA (p.K13del)
ISCN -
DB-ID ERCC3_000013
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) Retrieve
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 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ERCC3 NM_000122.1 ?/. - c.36_38del r.(?) p.(Lys13del)
MAP3K2 NM_006609.4 ?/. - c.*13868_*13870del r.(=) p.(=)


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