Genomic variant #0000020942

Individual ID 00017030
Chromosome 17
Allele Parent #2
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.29497013A>G
Reference -
DB-ID NF1_000191 See all 5 reported entries
dbSNP ID rs587778552
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 0.00087
Allele Count 5
Allele Number 5752
Owner Despoina Kalfakakou
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NF1 NM_000267.3 ?/? - c.584A>G r.(?) p.(Lys195Arg)
NF1 NM_001042492.2 ?/? - c.584A>G r.(?) p.(Lys195Arg)
NF1 NM_001128147.2 ?/? - c.584A>G r.(?) p.(Lys195Arg)



Screenings


AscendingScreening ID     

Template     

Technique     

Type     

Genes screened     

Variants found     

Owner     
0000000776 DNA SEQ-NG-I 1 - 5 Despoina Kalfakakou