Variant #0000193999 (NC_000004.11:g.72363294A>T, NM_001098484.2:c.2051A>T (SLC4A4))

Chromosome 4
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.72363294A>T
DNA change (hg38) g.71497577A>T
Published as -
ISCN -
DB-ID SLC4A4_000014 See all 2 reported entries
Variant remarks -
Reference PubMed: Yamazaki 2011
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00164 View details
Owner Mark Parker
Database submission license No license selected
Created by Mark Parker
Date created 2012-05-18 20:09:40 +02:00 (CEST)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC4A4 NM_001098484.2 -/. 16 c.2051A>T r.(?) p.(Ans684Ile)


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