Variant #0000800424 (NC_000002.11:g.220502366G>C, NM_005070.3:c.2599G>C (SLC4A3))

Chromosome 2
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.220502366G>C
DNA change (hg38) -
Published as SLC4A3(NM_001326559.2):c.2680G>C (p.D894H), SLC4A3(NM_005070.4):c.2599G>C (p.(Asp867His))
ISCN -
DB-ID SLC4A3_000007 See all 2 reported entries
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) 0.00965 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC4A3 NM_005070.3 -/. - c.2599G>C r.(?) p.(Asp867His)


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