Variant #0000223320 (NC_000013.10:g.23898509T>C, NM_000231.2:c.705T>C (SGCG))

Chromosome 13
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.23898509T>C
DNA change (hg38) g.23324370T>C
Published as -
ISCN -
DB-ID SGCG_000036 See all 10 reported entries
Variant remarks -
Reference from website {DBsub-Emory}
ClinVar ID -
dbSNP ID rs1800353
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.68658 View details
Owner Madhuri Hegde
Database submission license No license selected
Created by Madhuri Hegde
Date created 2012-10-26 15:26:18 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SGCG NM_000231.2 -/. 8 c.705T>C r.(?) p.(=)


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