Variant #0000223259 (NC_000017.10:g.48252804C>T, NM_000023.2:c.*6C>T (SGCA))

Chromosome 17
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.48252804C>T
DNA change (hg38) g.50175443C>T
Published as *6T>C
ISCN -
DB-ID SGCA_000047 See all 6 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 rs2696288
Origin Germline
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 15:17:26 +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     
SGCA NM_000023.2 -/. 9 c.*6C>T r.(?) p.(=)


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