Variant #0000618052 (NC_000020.10:g.3210062G>A, NM_032034.3:c.1827C>T (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.3210062G>A
DNA change (hg38) g.3229416G>A
Published as SLC4A11(NM_001174090.1):c.1908C>T (p.S636=)
ISCN -
DB-ID ITPA_000022
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) 0.00048 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
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.1779C>T r.(?) p.(Ser593=)
SLC4A11 NM_032034.3 -?/. - c.1827C>T r.(?) p.(Ser609=)
ITPA NM_033453.3 -?/. - c.*5954G>A r.(=) p.(=)


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