Genomic variant #0000008928

Individual ID 00021164
Chromosome 17
Allele Parent #2
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.29508699T>C
Reference -
DB-ID NF1_000101 See all 7 reported entries
dbSNP ID -
Genetic origin -
Segregation -
Is Greek Founder -
Average frequency (large NGS studies) Variant not found in online data sets
Average frequency in greek population 0.00168
Owner Despoina Kalfakakou
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NF1 NM_000267.3 ./. - c.655-29T>C r.(=) p.(=)
NF1 NM_001042492.2 ./. - c.655-29T>C r.(=) p.(=)
NF1 NM_001128147.2 ./. - c.655-29T>C r.(=) p.(=)



Screenings


AscendingScreening ID     

Template     

Technique     

Type     

Genes screened     

Variants found     

Owner     
0000000239 DNA SEQ-NG-I 1 - 9 Despoina Kalfakakou