Genomic variant #0000037066

Individual ID 00015968
Chromosome 11
Allele Parent #2
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.64575044C>T
Reference Teh et al (1998)  
DB-ID MEN1_000007 See all 2 reported entries
dbSNP ID rs104894268
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 0.00017
Allele Count 1
Allele Number 5796
Owner Despoina Kalfakakou
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MEN1 NM_000244.3 +/+ - c.778G>A r.(?) p.(Glu260Lys)
MEN1 NM_130799.2 +/+ - c.763G>A r.(?) p.(Glu255Lys)
MEN1 NM_130800.2 +/+ - c.778G>A r.(?) p.(Glu260Lys)
MEN1 NM_130801.2 +/+ - c.778G>A r.(?) p.(Glu260Lys)
MEN1 NM_130802.2 +/+ - c.778G>A r.(?) p.(Glu260Lys)
MEN1 NM_130803.2 +/+ - c.778G>A r.(?) p.(Glu260Lys)
MEN1 NM_130804.2 +/+ - c.778G>A r.(?) p.(Glu260Lys)



Screenings


AscendingScreening ID     

Template     

Technique     

Type     

Genes screened     

Variants found     

Owner     
0000004879 DNA SEQ-NG 0 - 1 Despoina Kalfakakou