Variant #0000680824 (NC_000017.10:g.30264363C>T, NM_015355.2:c.98C>T (SUZ12))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.30264363C>T
DNA change (hg38) -
Published as SUZ12(NM_015355.2):c.98C>T (p.(Ala33Val)), SUZ12(NM_015355.4):c.98C>T (p.A33V)
ISCN -
DB-ID SUZ12_000024 See all 2 reported entries
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) 0.0002 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +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.98C>T r.(?) p.(Ala33Val)


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