Variant #0000981416 (NC_000015.9:g.75656924_75656926del, NM_001145358.1:c.*7397_*7399del (SIN3A))

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.75656924_75656926del
DNA change (hg38) -
Published as MAN2C1(NM_006715.4):c.506_508del (p.(Lys169del))
ISCN -
DB-ID MAN2C1_000017
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 2024-04-19 20:27:30 +02:00 (CEST)
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.*7397_*7399del r.(=) p.(=)
MAN2C1 NM_006715.3 ?/. - c.506_508del r.(?) p.(Lys169del)


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