Variant #0000569413 (NC_000020.10:g.3208967C>T, NM_032034.3:c.2544G>A (SLC4A11))

Chromosome 20
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.3208967C>T
DNA change (hg38) g.3228321C>T
Published as SLC4A11(NM_001174089.1):c.2496G>A (p.(Met832Ile))
ISCN -
DB-ID ITPA_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) 0.00248 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC4A11 NM_001174089.1 -?/. - c.2496G>A r.(?) p.(Met832Ile)
SLC4A11 NM_032034.3 -?/. - c.2544G>A r.(?) p.(Met848Ile)
ITPA NM_033453.3 -?/. - c.*4859C>T r.(=) p.(=)


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