Variant #0000850655 (NC_000004.11:g.72338589A>G, NM_001098484.2:c.1805A>G (SLC4A4))

Chromosome 4
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.72338589A>G
DNA change (hg38) -
Published as SLC4A4(NM_001098484.2):c.1805A>G (p.K602R), SLC4A4(NM_001098484.3):c.1805A>G (p.(Lys602Arg)), SLC4A4(NM_003759.3):c.1673A>G (p.K558R)
ISCN -
DB-ID SLC4A4_000011 See all 5 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) 0.00211 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:40:45 +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     
SLC4A4 NM_001098484.2 -?/. - c.1805A>G r.(?) p.(Lys602Arg)


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