Variant #0001035798 (NC_000006.11:g.43405684G>C, NM_033450.2:c.1804G>C (ABCC10))

Chromosome 6
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.43405684G>C
DNA change (hg38) -
Published as ABCC10(NM_001198934.2):c.1888G>C (p.(Gly630Arg))
ISCN -
DB-ID ABCC10_000010
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) 2.0E-5 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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DLK2 NM_023932.2 ?/. - c.*12593C>G r.(=) p.(=)
ABCC10 NM_033450.2 ?/. - c.1804G>C r.(?) p.(Gly602Arg)


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