ClinVar Miner

List of variants in gene DPP6 reported by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 44
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_130797.4(DPP6):c.227A>T (p.Asp76Val) rs572667303 0.01073
NM_130797.4(DPP6):c.627+21101A>G rs117574002 0.00365
NM_130797.4(DPP6):c.1956C>T (p.Ser652=) rs184190456 0.00210
NM_130797.4(DPP6):c.1711A>C (p.Lys571Gln) rs140460765 0.00168
NM_130797.4(DPP6):c.235G>A (p.Glu79Lys) rs760726966 0.00005
NM_130797.4(DPP6):c.932C>T (p.Thr311Met) rs779028965 0.00003
NM_130797.4(DPP6):c.1480G>A (p.Asp494Asn) rs199958650 0.00001
NM_130797.4(DPP6):c.1635T>C (p.His545=) rs757845557 0.00001
NM_130797.4(DPP6):c.193G>T (p.Gly65Cys) rs879255429 0.00001
NM_130797.4(DPP6):c.194G>T (p.Gly65Val) rs879255430 0.00001
NM_130797.4(DPP6):c.1015G>T (p.Val339Leu)
NM_130797.4(DPP6):c.1213G>A (p.Val405Met)
NM_130797.4(DPP6):c.1221C>T (p.Ile407=)
NM_130797.4(DPP6):c.127C>G (p.Pro43Ala) rs1401359876
NM_130797.4(DPP6):c.132C>T (p.Leu44=)
NM_130797.4(DPP6):c.1370G>A (p.Arg457Gln)
NM_130797.4(DPP6):c.1446C>T (p.Ser482=)
NM_130797.4(DPP6):c.150G>A (p.Ala50=)
NM_130797.4(DPP6):c.1515G>A (p.Thr505=)
NM_130797.4(DPP6):c.167GCG[8] (p.Gly62dup) rs926747893
NM_130797.4(DPP6):c.1714+7G>C
NM_130797.4(DPP6):c.1802T>C (p.Ile601Thr)
NM_130797.4(DPP6):c.1914T>G (p.Ala638=)
NM_130797.4(DPP6):c.1941G>A (p.Thr647=)
NM_130797.4(DPP6):c.1964C>T (p.Ala655Val)
NM_130797.4(DPP6):c.2193G>A (p.Gln731=)
NM_130797.4(DPP6):c.225C>T (p.Ser75=)
NM_130797.4(DPP6):c.243+11150C>A
NM_130797.4(DPP6):c.243+7980G>A
NM_130797.4(DPP6):c.2532G>A (p.Val844=)
NM_130797.4(DPP6):c.2580G>A (p.Glu860=)
NM_130797.4(DPP6):c.27T>C (p.Thr9=)
NM_130797.4(DPP6):c.627+20797G>A
NM_130797.4(DPP6):c.627+20824C>T
NM_130797.4(DPP6):c.627+21029G>A
NM_130797.4(DPP6):c.627+21039A>G
NM_130797.4(DPP6):c.627+21114G>A
NM_130797.4(DPP6):c.666C>T (p.Ser222=)
NM_130797.4(DPP6):c.668A>G (p.Lys223Arg)
NM_130797.4(DPP6):c.680+6A>G
NM_130797.4(DPP6):c.744C>G (p.Gly248=)
NM_130797.4(DPP6):c.764T>C (p.Ile255Thr) rs1586968038
NM_130797.4(DPP6):c.949G>A (p.Ala317Thr)
NM_130797.4(DPP6):c.99C>G (p.Pro33=)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.