Variant #0000569416 (NC_000020.10:g.3209357C>T, NC_000020.10(NM_032034.3):c.2241-4G>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.3209357C>T
DNA change (hg38) g.3228711C>T
Published as SLC4A11(NM_001174089.1):c.2193-4G>A (p.?)
ISCN -
DB-ID ITPA_000003
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) 0.03752 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.2193-4G>A r.spl? p.?
SLC4A11 NM_032034.3 -?/. - c.2241-4G>A r.spl? p.?
ITPA NM_033453.3 -?/. - c.*5249C>T r.(=) p.(=)


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