Variant #0000223276 (NC_000004.11:g.52904446del, SGCB(NM_000232.4):c.-20del)

Chromosome 4
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.52904446del
DNA change (hg38) g.52038280del
Published as -20delG
ISCN -
DB-ID SGCB_000085
Variant remarks -
Reference from website {DBsub-Emory}
ClinVar ID -
dbSNP ID -
Origin Unknown
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 No license selected
Created by Madhuri Hegde
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SGCB NM_000232.4 -/. 1 c.-20del r.(?) p.(=)