"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "DPP6"[gene - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 57

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3026626	NM_001364497.2(DPP6):c.60+138721G>A	DPP6 (V16M)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2658246	NM_130797.4(DPP6):c.27T>C (p.Thr9=)	DPP6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2658247	NM_130797.4(DPP6):c.99C>G (p.Pro33=)	DPP6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1335703	NM_130797.4(DPP6):c.127C>G (p.Pro43Ala)	DPP6 (P43A)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2658248	NM_130797.4(DPP6):c.132C>T (p.Leu44=)	DPP6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3026004	NM_130797.4(DPP6):c.136C>T (p.Pro46Ser)	DPP6 (P46S)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2658249	NM_130797.4(DPP6):c.150G>A (p.Ala50=)	DPP6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 810229	NM_130797.4(DPP6):c.167GCG[8] (p.Gly62dup)	DPP6	Microsatellite (inframe_insertion +1 more)	not provided	GLikely benign
Select item 3025925	NM_130797.4(DPP6):c.183C>T (p.Gly61=)	DPP6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 252778	NM_130797.4(DPP6):c.193G>T (p.Gly65Cys)	DPP6 (G65C)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 252779	NM_130797.4(DPP6):c.194G>T (p.Gly65Val)	DPP6 (G65V)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 2658250	NM_130797.4(DPP6):c.225C>T (p.Ser75=)	DPP6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 252780	NM_130797.4(DPP6):c.227A>T (p.Asp76Val)	DPP6 (D76V)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 1695218	NM_130797.4(DPP6):c.235G>A (p.Glu79Lys)	DPP6 (E79K)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2658251	NM_130797.4(DPP6):c.243+5629A>G	DPP6, LOC101929998	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2658252	NM_130797.4(DPP6):c.243+7980G>A	DPP6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2658253	NM_130797.4(DPP6):c.243+11150C>A	DPP6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3025934	NM_130797.4(DPP6):c.580A>G (p.Ile194Val)	DPP6 (I130V +3 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2658254	NM_130797.4(DPP6):c.627+20797G>A	DPP6 (V231I)	Single nucleotide variant (missense variant +2 more)	not provided +1 more	GBenign
Select item 2658255	NM_130797.4(DPP6):c.627+20824C>T	DPP6 (H240Y)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 3025919	NM_130797.4(DPP6):c.627+20879G>A	DPP6 (R258H)	Single nucleotide variant (missense variant +2 more)	not provided	GLikely benign
Select item 2658256	NM_130797.4(DPP6):c.627+21029G>A	DPP6 (R308H)	Single nucleotide variant (missense variant +2 more)	not provided	GLikely benign
Select item 2658257	NM_130797.4(DPP6):c.627+21039A>G	DPP6	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 802383	NM_130797.4(DPP6):c.627+21101A>G	DPP6 (H332R)	Single nucleotide variant (missense variant +2 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2658258	NM_130797.4(DPP6):c.627+21114G>A	DPP6	Single nucleotide variant (synonymous variant +2 more)	not provided +1 more	GLikely benign
Select item 2658259	NM_130797.4(DPP6):c.666C>T (p.Ser222=)	DPP6	Single nucleotide variant (synonymous variant +2 more)	not provided	GBenign
Select item 2441027	NM_130797.4(DPP6):c.668A>G (p.Lys223Arg)	DPP6 (K159R +3 more)	Single nucleotide variant (missense variant +2 more)	not provided +1 more	GUncertain significance
Select item 2658260	NM_130797.4(DPP6):c.680+6A>G	DPP6	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2658261	NM_130797.4(DPP6):c.744C>G (p.Gly248=)	DPP6	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 810232	NM_130797.4(DPP6):c.764T>C (p.Ile255Thr)	DPP6 (I148T +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3026020	NM_130797.4(DPP6):c.804C>T (p.Val268=)	DPP6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3067450	NM_130797.4(DPP6):c.924G>A (p.Pro308=)	DPP6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 872358	NM_130797.4(DPP6):c.932C>T (p.Thr311Met)	DPP6 (T204M +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3041146	NM_130797.4(DPP6):c.939C>T (p.Leu313=)	DPP6	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 3026390	NM_130797.4(DPP6):c.940G>A (p.Ala314Thr)	DPP6 (A207T +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2658262	NM_130797.4(DPP6):c.949G>A (p.Ala317Thr)	DPP6 (A210T +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2658263	NM_130797.4(DPP6):c.1015G>T (p.Val339Leu)	DPP6 (V232L +4 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign
Select item 2658264	NM_130797.4(DPP6):c.1213G>A (p.Val405Met)	DPP6 (V298M +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2658265	NM_130797.4(DPP6):c.1221C>T (p.Ile407=)	DPP6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2499064	NM_130797.4(DPP6):c.1370G>A (p.Arg457Gln)	DPP6 (R350Q +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 3026401	NM_130797.4(DPP6):c.1410C>T (p.Pro470=)	DPP6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2658266	NM_130797.4(DPP6):c.1446C>T (p.Ser482=)	DPP6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1012587	NM_130797.4(DPP6):c.1480G>A (p.Asp494Asn)	DPP6 (D387N +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2658267	NM_130797.4(DPP6):c.1515G>A (p.Thr505=)	DPP6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1335704	NM_130797.4(DPP6):c.1635T>C (p.His545=)	DPP6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 218491	NM_130797.4(DPP6):c.1711A>C (p.Lys571Gln)	DPP6 (K507Q +4 more)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 2658268	NM_130797.4(DPP6):c.1714+7G>C	DPP6	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2658269	NM_130797.4(DPP6):c.1802T>C (p.Ile601Thr)	DPP6 (I494T +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2673138	NM_130797.4(DPP6):c.1914T>G (p.Ala638=)	DPP6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2658270	NM_130797.4(DPP6):c.1941G>A (p.Thr647=)	DPP6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 810235	NM_130797.4(DPP6):c.1956C>T (p.Ser652=)	DPP6	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2658271	NM_130797.4(DPP6):c.1964C>T (p.Ala655Val)	DPP6 (A548V +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 3027026	NM_130797.4(DPP6):c.1979G>A (p.Cys660Tyr)	DPP6 (C553Y +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2571303	NM_130797.4(DPP6):c.2193G>A (p.Gln731=)	DPP6	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 3024876	NM_130797.4(DPP6):c.2331C>T (p.Ser777=)	DPP6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2658272	NM_130797.4(DPP6):c.2532G>A (p.Val844=)	DPP6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2658273	NM_130797.4(DPP6):c.2580G>A (p.Glu860=)	DPP6	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 57