Variant #0000223313 (NC_000007.13:g.94252712A>G, NC_000007.13(NM_003919.2):c.391-3T>C (SGCE))

Chromosome 7
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.94252712A>G
DNA change (hg38) g.94623400A>G
Published as -
ISCN -
DB-ID SGCE_000050 See all 4 reported entries
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) 0.01967 View details
Owner Madhuri Hegde
Database submission license No license selected
Created by Madhuri Hegde
Date created 2012-10-26 15:21:21 +02:00 (CEST)
Date last edited 2020-06-11 10:40:17 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SGCE NM_003919.2 -/. 3i c.391-3T>C r.(?) p.(=)


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