Variant #0000555509 (NC_000015.9:g.75705323_75705327del, NM_001145358.1:c.533_537del (SIN3A))

Chromosome 15
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.75705323_75705327del
DNA change (hg38) g.75412982_75412986del
Published as SIN3A(NM_001145358.1):c.533_537delTGATA (p.(Leu178fs))
ISCN -
DB-ID SIN3A_000016
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SIN3A NM_001145358.1 +?/. - c.533_537del r.(?) p.(Leu178HisfsTer14)


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