Variant #0000154153 (NC_000005.9:g.176813499T>C, NM_003052.4:c.464T>C (SLC34A1))

Chromosome 5
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.176813499T>C
DNA change (hg38) g.177386498T>C
Published as -
ISCN -
DB-ID SLC34A1_000012 See all 3 reported entries
Variant remarks cDNA expression cloning in Xenopus oocytes showed no induced P-uptake/in Opossum kidney cells showed complete intra-cellular retention and no actin co-localisation
Reference PubMed: Schlingmann 2016, Journal: Schlingmann 2016
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2017-01-07 11:59:01 +01:00 (CET)
Date last edited 2025-03-02 18:13:14 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC34A1 NM_003052.4 +/. 5 c.464T>C r.(?) p.Leu155Pro


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