Variant #0000020799 (NC_000007.13:g.25163594A>G, NM_018947.5:c.145T>C (CYCS))

Chromosome 7
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.25163594A>G
DNA change (hg38) g.25123975A>G
Published as -
ISCN -
DB-ID CYCS_000001
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Anna Savoia
Database submission license No license selected
Created by Anna Savoia
Date created 2013-09-11 14:37:12 +02:00 (CEST)
Date last edited 2013-10-11 20:15:39 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CYCS NM_018947.5 ?/? 2 c.145T>C r.(?) p.(Tyr49His)


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