Variant #0001056834 (NC_000020.10:g.3211171G>A, NM_032034.3:c.1453C>T (SLC4A11))

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.3211171G>A
DNA change (hg38) -
Published as SLC4A11(NM_001174089.2):c.1405C>T (p.(Leu469Phe))
ISCN -
DB-ID SLC4A11_000114
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     
SLC4A11 NM_001174089.1 ?/. - c.1405C>T r.(?) p.(Leu469Phe)
SLC4A11 NM_032034.3 ?/. - c.1453C>T r.(?) p.(Leu485Phe)
ITPA NM_033453.3 ?/. - c.*7063G>A r.(=) p.(=)


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