Genomic variant #0000001126

Individual ID 00021048
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.29508818G>T
Reference -
DB-ID NF1_000024 See all 8 reported entries
dbSNP ID -
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 0.00139
Allele Count 8
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.730+15G>T r.(=) p.(=)
NF1 NM_001042492.2 ?/? - c.730+15G>T r.(=) p.(=)
NF1 NM_001128147.2 ?/? - c.730+15G>T r.(=) p.(=)



Screenings


AscendingScreening ID     

Template     

Technique     

Type     

Genes screened     

Variants found     

Owner     
0000000028 DNA SEQ-NG-I 1 - 16 Despoina Kalfakakou