Variant #0000465216 (NC_000004.11:g.52904414_52904416dup, SGCB(NM_000232.4):c.21_23dup)

Individual ID 00220275
Chromosome 4
Allele Parent #1
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.52904414_52904416dup
DNA change (hg38) g.52038248_52038250dup
Published as 21_23dupGGC
ISCN -
DB-ID SGCB_000071 See all 10 reported entries
Variant remarks no second variant
Reference PubMed: Nallamilli 2018
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Madhuri Hegde
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SGCB NM_000232.4 ?/. 1 c.21_23dup r.(?) p.(Ala9dup)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000221346 DNA SEQ;SEQ-NG - targeted gene panel - 4 Madhuri Hegde