"Ambry Genetics"[submitter] AND "GPR142"[gene] - ClinVar

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

Search results

Items: 45

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3101442	NM_001331076.1(GPR142):c.-333A>C	GPR142 (Q10H)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GLikely benign
Select item 2483922	NM_001331076.1(GPR142):c.-263G>A	GPR142 (E34K)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3101438	NM_001331076.1(GPR142):c.-259A>G	GPR142 (D35G)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3101441	NM_001331076.1(GPR142):c.-178C>G	GPR142 (T62R)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2338591	NM_001331076.1(GPR142):c.-162C>A	GPR142 (D67E)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3282219	NM_001331076.1(GPR142):c.-157G>A	GPR142 (R69Q)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3282215	NM_001331076.1(GPR142):c.-124G>A	GPR142 (R80H)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3282212	NM_001331076.1(GPR142):c.-58A>G	GPR142 (K87E)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2604663	NM_001331076.1(GPR142):c.-4G>A	GPR142 (G105S)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2358064	NM_001331076.1(GPR142):c.21G>A (p.Gly7=)	GPR142 (G113R)	Single nucleotide variant (synonymous variant +1 more)	not specified	GUncertain significance
Select item 2374578	NM_001331076.1(GPR142):c.140G>A (p.Gly47Glu)	GPR142 (G47E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2367862	NM_001331076.1(GPR142):c.178G>A (p.Ala60Thr)	GPR142 (A148T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2553327	NM_001331076.1(GPR142):c.245G>A (p.Gly82Glu)	GPR142 (G82E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371689	NM_001331076.1(GPR142):c.268G>A (p.Ala90Thr)	GPR142 (A90T +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2393735	NM_001331076.1(GPR142):c.308C>T (p.Pro103Leu)	GPR142 (P191L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2315262	NM_001331076.1(GPR142):c.354C>G (p.Ile118Met)	GPR142 (I206M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272964	NM_001331076.1(GPR142):c.367G>A (p.Val123Met)	GPR142 (V123M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389725	NM_001331076.1(GPR142):c.431G>A (p.Arg144His)	GPR142 (R144H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2392373	NM_001331076.1(GPR142):c.433A>G (p.Thr145Ala)	GPR142 (T145A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589002	NM_001331076.1(GPR142):c.439A>G (p.Asn147Asp)	GPR142 (N235D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350607	NM_001331076.1(GPR142):c.466G>A (p.Ala156Thr)	GPR142 (A156T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2372774	NM_001331076.1(GPR142):c.481G>A (p.Ala161Thr)	GPR142 (A161T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2556365	NM_001331076.1(GPR142):c.536G>A (p.Arg179Gln)	GPR142 (R267Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2411982	NM_001331076.1(GPR142):c.541G>A (p.Ala181Thr)	GPR142 (A269T +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3101444	NM_001331076.1(GPR142):c.551C>G (p.Pro184Arg)	GPR142 (P184R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2259892	NM_001331076.1(GPR142):c.563G>A (p.Arg188His)	GPR142 (R188H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101445	NM_001331076.1(GPR142):c.644C>G (p.Thr215Ser)	GPR142 (T303S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2454373	NM_001331076.1(GPR142):c.646G>A (p.Asp216Asn)	GPR142 (D304N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101446	NM_001331076.1(GPR142):c.721T>C (p.Phe241Leu)	GPR142 (F241L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2376199	NM_001331076.1(GPR142):c.752G>A (p.Arg251Gln)	GPR142 (R251Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101437	NM_001331076.1(GPR142):c.769C>T (p.Arg257Trp)	GPR142 (R257W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282211	NM_001331076.1(GPR142):c.787C>T (p.Arg263Trp)	GPR142 (R263W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2455130	NM_001331076.1(GPR142):c.788G>A (p.Arg263Gln)	GPR142 (R351Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282220	NM_001331076.1(GPR142):c.829C>G (p.Leu277Val)	GPR142 (L365V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282214	NM_001331076.1(GPR142):c.848C>T (p.Ala283Val)	GPR142 (A371V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101439	NM_001331076.1(GPR142):c.909G>T (p.Arg303Ser)	GPR142 (R391S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3101440	NM_001331076.1(GPR142):c.914A>G (p.His305Arg)	GPR142 (H393R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400411	NM_001331076.1(GPR142):c.956C>T (p.Thr319Met)	GPR142 (T319M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282216	NM_001331076.1(GPR142):c.959C>T (p.Ala320Val)	GPR142 (A408V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2322698	NM_001331076.1(GPR142):c.965A>G (p.Asn322Ser)	GPR142 (N322S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2276605	NM_001331076.1(GPR142):c.970G>T (p.Gly324Cys)	GPR142 (G412C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460604	NM_001331076.1(GPR142):c.1013G>A (p.Arg338Gln)	GPR142 (R338Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282213	NM_001331076.1(GPR142):c.1027G>A (p.Asp343Asn)	GPR142 (D343N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282218	NM_001331076.1(GPR142):c.1121T>C (p.Val374Ala)	GPR142 (V462A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3282217	NM_001331076.1(GPR142):c.1121T>G (p.Val374Gly)	GPR142 (V462G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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: 45