Genomic variant #0000224836

Individual ID 00133894
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.23898693C>T
DNA change (hg38) g.23324554C>T
Published as -
ISCN -
DB-ID SGCG_000038 See all 4 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs9510701
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) 0.0569 View details
Owner Ieke Ginjaar
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SGCG NM_000231.2 -/. 8 c.*13C>T r.(?) p.(=)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000134732 DNA SSCA;SEQ - - SGCG 3 Ieke Ginjaar