Variant #0000613141 (NC_000011.9:g.124500693T>C, NM_032811.2:c.889T>C (TBRG1))

Chromosome 11
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.124500693T>C
DNA change (hg38) g.124630797T>C
Published as TBRG1(NM_032811.3):c.889T>C (p.S297P)
ISCN -
DB-ID SIAE_000006
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 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 2019-12-04 15:24:38 +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     
SPA17 NM_017425.3 ?/. - c.-43183T>C r.(?) p.(=)
TBRG1 NM_032811.2 ?/. - c.889T>C r.(?) p.(Ser297Pro)
SIAE NM_170601.4 ?/. - c.*6154A>G r.(=) p.(=)


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