Variant #0001046190 (NC_000009.11:g.140128923C>T, NM_080877.2:c.1149C>T (SLC34A3))

Chromosome 9
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.140128923C>T
DNA change (hg38) -
Published as SLC34A3(NM_080877.2):c.1149C>T (p.A383=)
ISCN -
DB-ID RNF224_000035
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) 0.00236 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 2025-07-08 13:22:38 +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     
RNF224 NM_001190228.1 -/. - c.*5385C>T r.(=) p.(=)
SLC34A3 NM_080877.2 -/. - c.1149C>T r.(?) p.(=)


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