Variant #0000282460 (NC_000006.11:g.131917741G>A, NM_000045.3:c.*12693G>A (ARG1))

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.131917741G>A
DNA change (hg38) g.131596601G>A
Published as MED23(NM_004830.4):c.2695C>T (p.R899*)
ISCN -
DB-ID MED23_000004
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) 1.0E-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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARG1 NM_000045.3 ?/. - c.*12693G>A r.(=) p.(=)
MED23 NM_004830.3 ?/. - c.2695C>T r.(?) p.(Arg899Ter)
MED23 NM_015979.3 ?/. - c.2713C>T r.(?) p.(Arg905Ter)


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