Variant #0000975021 (NC_000002.11:g.220493861C>T, NC_000002.11(NM_005070.3):c.218-5C>T (SLC4A3))

Chromosome 2
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.220493861C>T
DNA change (hg38) -
Published as SLC4A3(NM_001326559.2):c.218-5C>T, SLC4A3(NM_005070.4):c.218-5C>T
ISCN -
DB-ID SLC4A3_000001 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) 0.00301 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 2024-04-19 20:20:39 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC4A3 NM_005070.3 -?/. - c.218-5C>T r.spl? p.?


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