Variant #0000308202 (NC_000020.10:g.35243756C>T, NM_018840.4:c.*3302C>T (C20orf24))

Chromosome 20
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.35243756C>T
DNA change (hg38) g.36615353C>T
Published as SLA2(NM_032214.3):c.404G>A (p.R135H)
ISCN -
DB-ID SLA2_000002
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) 0.0002 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TGIF2-C20orf24 NM_001199535.1 ?/. - c.*3302C>T r.(=) p.(=)
C20orf24 NM_018840.4 ?/. - c.*3302C>T r.(=) p.(=)
TGIF2 NM_021809.6 ?/. - c.*23922C>T r.(=) p.(=)
SLA2 NM_175077.2 ?/. - c.404G>A r.(?) p.(Arg135His)


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