Variant #0000997734 (NC_000009.11:g.140130521C>T, NM_080877.2:c.1453C>T (SLC34A3))

Chromosome 9
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.140130521C>T
DNA change (hg38) -
Published as SLC34A3(NM_001177316.1):c.1453C>T (p.(Arg485Cys)), SLC34A3(NM_080877.3):c.1453C>T (p.R485C)
ISCN -
DB-ID SLC34A3_000018 See all 3 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) 0.00058 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2024-08-28 13:16:32 +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     
SLC34A3 NM_080877.2 +?/. - c.1453C>T r.(?) p.(Arg485Cys)


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