Variant #0000223321 (NC_000013.10:g.23898664G>A, NM_000231.2:c.860G>A (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.23898664G>A
DNA change (hg38) g.23324525G>A
Published as 860A>G
ISCN -
DB-ID SGCG_000037 See all 11 reported entries
Variant remarks Variant Error [EREF/EREF]: This genomic variant does not match the reference sequence; the transcript variant does not match the reference sequence either. Please fix this entry and then remove this message.
Reference from website {DBsub-Emory}
ClinVar ID -
dbSNP ID rs1800354
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 15:26:18 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SGCG NM_000231.2 -/. 8 c.860G>A r.(?) p.(Ser287Asn)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.