Variant #0001055529 (NC_000016.9:g.30215182G>A, NM_001014999.2:c.*6395G>A (SLX1A))

Chromosome 16
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.30215182G>A
DNA change (hg38) -
Published as SULT1A3(NM_177552.4):c.829G>A (p.(Asp277Asn))
ISCN -
DB-ID SLX1A_000001
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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLX1A NM_001014999.2 ?/. - c.*6395G>A r.(=) p.(=)
SULT1A3 NM_177552.3 ?/. - c.829G>A r.(?) p.(Asp277Asn)
SLX1A-SULT1A3 NR_037608.1 ?/. - n.1750G>A r.(?) -


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