Genomic variant #0000006465

Individual ID 00021124
Chromosome 11
Allele Parent #2
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.64573115G>C
Reference -
DB-ID MEN1_000010
dbSNP ID rs1060499984
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.1192C>G r.(?) p.(Gln398Glu)
MEN1 NM_130799.2 ?/? - c.1177C>G r.(?) p.(Gln393Glu)
MEN1 NM_130800.2 ?/? - c.1192C>G r.(?) p.(Gln398Glu)
MEN1 NM_130801.2 ?/? - c.1192C>G r.(?) p.(Gln398Glu)
MEN1 NM_130802.2 ?/? - c.1192C>G r.(?) p.(Gln398Glu)
MEN1 NM_130803.2 ?/? - c.1192C>G r.(?) p.(Gln398Glu)
MEN1 NM_130804.2 ?/? - c.1192C>G r.(?) p.(Gln398Glu)



Screenings


AscendingScreening ID     

Template     

Technique     

Type     

Genes screened     

Variants found     

Owner     
0000000177 DNA SEQ-NG-I 1 - 11 Despoina Kalfakakou