Variant #0001037379 (NC_000009.11:g.140128584_140128602dup, NM_080877.2:c.949_967dup (SLC34A3))

Chromosome 9
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.140128584_140128602dup
DNA change (hg38) -
Published as SLC34A3(NM_001177316.2):c.949_967dup (p.(Val323Glyfs*276))
ISCN -
DB-ID RNF224_000032
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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.*5046_*5064dup r.(=) p.(=)
SLC34A3 NM_080877.2 ?/. - c.949_967dup r.(?) p.(Val323Glyfs*276)


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