Variant #0000315937 (NC_000017.10:g.30323860_30323861del, NM_015355.2:c.1838_1839del (SUZ12))

Chromosome 17
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.30323860_30323861del
DNA change (hg38) g.31996841_31996842del
Published as SUZ12(NM_015355.3):c.1838_1839delTG (p.V613Dfs*16)
ISCN -
DB-ID SUZ12_000002
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-13 12:08:16 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SUZ12 NM_015355.2 ?/. - c.1838_1839del r.(?) p.(Val613AspfsTer16)


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