Related gene-specific medical variations for Gene (Select 22990) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2644348	NM_014982.3(PCNX1):c.51C>T (p.Leu17=)	LOC130056009, PCNX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2412001	NM_014982.3(PCNX1):c.12G>C (p.Gln4His)	LOC130056009, PCNX1 (Q4H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362920	NM_014982.3(PCNX1):c.5201A>G (p.Asn1734Ser)	LOC126861988, PCNX1 (N1734S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1340921	GRCh37/hg19 14q24.2(chr14:71415706-71716923)x3	PCNX1	Copy number gain	not provided	GLikely benign
Select item 755384	NM_014982.3(PCNX1):c.5133G>A (p.Ser1711=)	LOC126861988, PCNX1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 161686	NM_014982.3(PCNX1):c.3049G>T (p.Ala1017Ser)	PCNX1 (A1017S +1 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance

ClinVar