Variant #0001014623 (NC_000010.10:g.50724761C>T, NC_000010.10(NM_000124.2):c.1397+7318G>A (ERCC6))

Chromosome 10
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.50724761C>T
DNA change (hg38) -
Published as ERCC6(NM_001277058.2):c.1804G>A (p.D602N)
ISCN -
DB-ID ERCC6_000155
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) 9.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-10-29 21:08:56 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ERCC6 NM_000124.2 ?/. - c.1397+7318G>A r.(=) p.(=)
PGBD3 NM_170753.2 ?/. - c.400G>A r.(?) p.(Asp134Asn)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.