Genomic variant #0000039688

Individual ID 00020642
Chromosome 10
Allele Maternal (inferred)
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.43614996G>A
Reference -
DB-ID RET_000112 See all 2 reported entries
dbSNP ID rs79658334
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 0.00034
Allele Count 2
Allele Number 5866
Owner Despoina Kalfakakou
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RET NM_020630.4 +/+ - c.2410G>A r.(?) p.(Val804Met)
RET NM_020975.4 +/+ - c.2410G>A r.(?) p.(Val804Met)



Screenings


AscendingScreening ID     

Template     

Technique     

Type     

Genes screened     

Variants found     

Owner     
0000006675 DNA SEQ 1 RET 1 Despoina Kalfakakou