Variant #0000194018 (NC_000004.11:g.72338589A>G, NM_001098484.2:c.1805A>G (SLC4A4))

Chromosome 4
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.72338589A>G
DNA change (hg38) g.71472872A>G
Published as -
ISCN -
DB-ID SLC4A4_000011 See all 5 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs72650362
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00211 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 N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC4A4 NM_001098484.2 ?/. 14 c.1805A>G r.(?) p.(Lys602Arg)


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