Variant #0000804022 (NC_000009.11:g.140128688_140128695del, NM_080877.2:c.1053_1060del (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.140128688_140128695del
DNA change (hg38) -
Published as SLC34A3(NM_001177317.1):c.1053_1060delCGGCCGCG (p.R353Pfs*237)
ISCN -
DB-ID RNF224_000015
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +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.*5150_*5157del r.(=) p.(=)
SLC34A3 NM_080877.2 +?/. - c.1053_1060del r.(?) p.(Arg353Profs*237)


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