Variant #0000681592 (NC_000020.10:g.3214819T>G, NM_032034.3:c.481A>C (SLC4A11))

Chromosome 20
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.3214819T>G
DNA change (hg38) -
Published as SLC4A11(NM_032034.4):c.481A>C (p.R161=)
ISCN -
DB-ID SLC4A11_000094
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) 0.43707 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +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.433A>C r.(?) p.(Arg145=)
SLC4A11 NM_032034.3 -/. - c.481A>C r.(?) p.(Arg161=)


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