Variant #0000324219 (NC_000015.9:g.75941966C>T, NM_153271.1:c.523C>T (SNX33))

Chromosome 15
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.75941966C>T
DNA change (hg38) g.75649625C>T
Published as SNX33(NM_153271.1):c.523C>T (p.(Arg175Ter))
ISCN -
DB-ID SNX33_000003
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-06 17:16:33 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IMP3 NM_018285.3 ?/. - c.-9457G>A r.(?) p.(=)
SNX33 NM_153271.1 ?/. - c.523C>T r.(?) p.(Arg175Ter)


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