Genomic variant #0000018146

Individual ID 00016829
Chromosome 2
Allele Parent #2
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.48033423A>T
Reference -
DB-ID MSH6_000034 See all 2 reported entries
dbSNP ID rs147453999
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 0.00035
Allele Count 2
Allele Number 5762
Owner Despoina Kalfakakou
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MSH6 NM_000179.2 ?/? - c.3727A>T r.(?) p.(Thr1243Ser)
MSH6 NM_001281492.1 ?/? - c.3337A>T r.(?) p.(Thr1113Ser)
MSH6 NM_001281493.1 ?/? - c.2821A>T r.(?) p.(Thr941Ser)
MSH6 NM_001281494.1 ?/? - c.2821A>T r.(?) p.(Thr941Ser)



Screenings


AscendingScreening ID     

Template     

Technique     

Type     

Genes screened     

Variants found     

Owner     
0000000548 DNA SEQ-NG-I 1 - 7 Despoina Kalfakakou