Genomic variant #0000041846

Individual ID 00022042
Chromosome 9
Allele Parent #2
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.21970916C>T
Reference -
DB-ID CDKN2A_000030 See all 13 reported entries
dbSNP ID rs3731249
Variant remarks -
Genetic origin -
Segregation -
Also Known As -
Is Greek Founder -
Geographic Origin (for founder variants) -
Average frequency (large NGS studies) Retrieve
Average frequency in greek population 0.0022
Allele Count 13
Allele Number 5902
Owner Stevi Xera
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CDKN2A NM_000077.4 ./. - c.442G>A r.(?) p.(Ala148Thr)
CDKN2A NM_001195132.1 ./. - c.442G>A r.(?) p.(Ala148Thr)
CDKN2A NM_058195.3 ./. - c.*86G>A r.(=) p.(=)
CDKN2A NM_058197.4 ./. - c.*365G>A r.(=) p.(=)



Screenings


AscendingScreening ID     

Template     

Technique     

Type     

Genes screened     

Variants found     

Owner     
0000007539 DNA SEQ-NG-I 1 - 40 Stevi Xera