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

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 -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Madhuri Hegde
Database submission license No license selected
Created by Madhuri Hegde
Date created 2012-10-26 15:19:20 +02:00 (CEST)
Date last edited 2020-06-16 13:00:06 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

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


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