Variant #0001027541 (NC_000005.9:g.60205799_60205801del, NC_000005.9(NM_000082.3):c.400-5091_400-5089del (ERCC8))

Chromosome 5
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.60205799_60205801del
DNA change (hg38) -
Published as -
ISCN -
DB-ID ERCC8_000033
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs768280897
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-02-08 01:50:02 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ERCC8 NM_000082.3 +?/. - c.400-5091_400-5089del r.(?) p.(?)


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