Variant #0000223315 (NC_000007.13:g.94257662del, NM_003919.2:c.242del (SGCE))

Chromosome 7
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic (paternal)
DNA change (genomic) (Relative to hg19 / GRCh37) g.94257662del
DNA change (hg38) g.94628350del
Published as -
ISCN -
DB-ID SGCE_000058
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 15:21:20 +02:00 (CEST)
Date last edited 2021-07-01 09:21:35 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SGCE NM_003919.2 +/. 3 c.242del r.(?) p.(Ser81Ilefs*5)


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