Variant #0001025181 (NC_000006.11:g.157099176C>T, NM_020732.3:c.113C>T (ARID1B))

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.157099176C>T
DNA change (hg38) -
Published as ARID1B(NM_001371656.1):c.362C>T (p.S121F)
ISCN -
DB-ID ARID1B_000579
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-02-07 18:57:27 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARID1B NM_001374828.1 ?/. - c.362C>T r.(?) p.(Ser121Phe)
ARID1B NM_020732.3 ?/. - c.113C>T r.(?) p.(Ser38Phe)


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