Related gene-specific medical variations for Gene (Select 2863) - ClinVar

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Items: 24

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3121675	NM_144586.7(LYPD1):c.421T>G (p.Cys141Gly)	GPR39, LYPD1 (C141G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3121674	NM_144586.7(LYPD1):c.379A>C (p.Thr127Pro)	GPR39, LYPD1 (T75P +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101767	NM_001508.3(GPR39):c.880G>T (p.Val294Leu)	GPR39, LYPD1 (V294L)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3101763	NM_001508.3(GPR39):c.1316C>T (p.Pro439Leu)	GPR39, LYPD1 (P439L)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3101762	NM_001508.3(GPR39):c.1301A>G (p.Asn434Ser)	GPR39, LYPD1 (N434S)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3101761	NM_001508.3(GPR39):c.1149C>A (p.Asp383Glu)	GPR39, LYPD1 (D383E)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2621004	NM_001508.3(GPR39):c.1040C>T (p.Ser347Phe)	GPR39, LYPD1 (S347F)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2601732	NM_001508.3(GPR39):c.1097A>C (p.Gln366Pro)	GPR39, LYPD1 (Q366P)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 2600185	NM_001508.3(GPR39):c.1268C>G (p.Ser423Cys)	GPR39, LYPD1 (S423C)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2522288	NM_001508.3(GPR39):c.1189C>T (p.Arg397Trp)	GPR39, LYPD1 (R397W)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GLikely benign
Select item 2492973	NM_001508.3(GPR39):c.955T>C (p.Phe319Leu)	GPR39, LYPD1 (F319L)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2399651	NM_001508.3(GPR39):c.1177C>T (p.Leu393Phe)	GPR39, LYPD1 (L393F)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2399650	NM_001508.3(GPR39):c.1176G>T (p.Leu392Phe)	GPR39, LYPD1 (L392F)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2382895	NM_001508.3(GPR39):c.1309G>T (p.Ala437Ser)	GPR39, LYPD1 (A437S)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2332107	NM_001508.3(GPR39):c.1094T>G (p.Leu365Arg)	GPR39, LYPD1 (L365R)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2332106	NM_001508.3(GPR39):c.1093C>A (p.Leu365Met)	GPR39, LYPD1 (L365M)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2329825	NM_001508.3(GPR39):c.1135C>T (p.His379Tyr)	GPR39, LYPD1 (H379Y)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2264168	NM_001508.3(GPR39):c.1230A>T (p.Leu410Phe)	GPR39, LYPD1 (L410F)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2259247	NM_001508.3(GPR39):c.1097A>G (p.Gln366Arg)	GPR39, LYPD1 (Q366R)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2242502	NM_001508.3(GPR39):c.1160T>G (p.Phe387Cys)	GPR39, LYPD1 (F387C)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2221234	NM_001508.3(GPR39):c.1172C>G (p.Pro391Arg)	GPR39, LYPD1 (P391R)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 783984	NM_001508.3(GPR39):c.879C>A (p.Ala293=)	GPR39, LYPD1	Single nucleotide variant (3 prime UTR variant +1 more)	not provided	GBenign
Select item 712363	NM_001508.3(GPR39):c.1264_1266dup (p.Lys422dup)	GPR39, LYPD1	Duplication (3 prime UTR variant +1 more)	not provided	GBenign
Select item 218591	NM_001508.3(GPR39):c.1132G>A (p.Ala378Thr)	GPR39, LYPD1 (A378T)	Single nucleotide variant (3 prime UTR variant +1 more)	not provided +1 more	GConflicting classifications of pathogenicity

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Links from Gene

Items: 24