Variant #0001033242 (NC_000002.11:g.27430239G>A, NM_021095.2:c.280C>T (SLC5A6))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.27430239G>A
DNA change (hg38) -
Published as SLC5A6(NM_021095.4):c.280C>T (p.(Arg94*))
ISCN -
DB-ID SLC5A6_000007 See all 3 reported entries
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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATRAID NM_016085.4 +/. - c.-5312G>A r.(?) p.(=)
SLC5A6 NM_021095.2 +/. - c.280C>T r.(?) p.(Arg94*)


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