Variant #0000975195 (NC_000002.11:g.27430385T>C, NM_021095.2:c.134A>G (SLC5A6))

Chromosome 2
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.27430385T>C
DNA change (hg38) -
Published as SLC5A6(NM_021095.4):c.134A>G (p.(Tyr45Cys))
ISCN -
DB-ID ATRAID_000005
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:20:39 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATRAID NM_016085.4 ?/. - c.-5166T>C r.(?) p.(=)
SLC5A6 NM_021095.2 ?/. - c.134A>G r.(?) p.(Tyr45Cys)


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