Variant #0000950446 (NC_000015.9:g.75684668_75684669del, NM_001145358.1:c.2773_2774del (SIN3A))

Chromosome 15
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.75684668_75684669del
DNA change (hg38) -
Published as SIN3A(NM_001145358.2):c.2773_2774delGA (p.E925Mfs*14)
ISCN -
DB-ID SIN3A_000062
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SIN3A NM_001145358.1 +/. - c.2773_2774del r.(?) p.(Glu925Metfs*14)


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