Variant #0000927156 (NC_000022.10:g.32480561G>A, NM_000343.3:c.800G>A (SLC5A1))

Chromosome 22
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.32480561G>A
DNA change (hg38) -
Published as SLC5A1(NM_000343.3):c.800G>A (p.R267Q), SLC5A1(NM_000343.4):c.800G>A (p.R267Q)
ISCN -
DB-ID SLC5A1_000011 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) 1.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-04-16 21:50:28 +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     
SLC5A1 NM_000343.3 +?/. - c.800G>A r.(?) p.(Arg267Gln)


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