Genomic variant #0000038756

Individual ID 00016863
Chromosome 16
Allele Parent #2
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.2121909C>T
Reference -
DB-ID TSC2_000016 See all 3 reported entries
dbSNP ID rs760489473
Variant remarks -
Genetic origin Germline
Segregation -
Also Known As -
Is Greek Founder -
Geographic Origin (for founder variants) -
Average frequency (large NGS studies) Variant not found in online data sets
Average frequency in greek population 0.00052
Allele Count 3
Allele Number 5752
Owner Despoina Kalfakakou
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TSC2 NM_000548.3 ?/? - c.2071C>T r.(?) p.(Arg691Cys)
TSC2 NM_001077183.1 ?/? - c.2071C>T r.(?) p.(Arg691Cys)
TSC2 NM_001114382.1 ?/? - c.2071C>T r.(?) p.(Arg691Cys)



Screenings


AscendingScreening ID     

Template     

Technique     

Type     

Genes screened     

Variants found     

Owner     
0000006912 DNA SEQ-NG-I 1 - 10 Despoina Kalfakakou