Variant #0000223314 (NC_000007.13:g.94259173A>G, NC_000007.13(NM_003919.2):c.110-20T>C (SGCE))

Chromosome 7
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.94259173A>G
DNA change (hg38) g.94629861A>G
Published as -
ISCN -
DB-ID SGCE_000057
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 2020-06-11 10:41:05 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SGCE NM_003919.2 ?/. 1i c.110-20T>C r.(?) p.(=)


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