Related gene-specific medical variations for Gene (Select 50512) - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3216197	NM_015720.4(PODXL2):c.1710C>G (p.Ser570Arg)	LOC129937492, PODXL2 (S570R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3216196	NM_015720.4(PODXL2):c.1705C>T (p.Pro569Ser)	LOC129937492, PODXL2 (P569S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3216195	NM_015720.4(PODXL2):c.1695G>C (p.Gln565His)	LOC129937492, PODXL2 (Q565H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3216194	NM_015720.4(PODXL2):c.1692G>T (p.Met564Ile)	LOC129937492, PODXL2 (M564I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3216192	NM_015720.4(PODXL2):c.1625G>A (p.Arg542His)	LOC129937491, PODXL2 (R542H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2614934	NM_015720.4(PODXL2):c.1649A>T (p.Asp550Val)	LOC129937491, PODXL2 (D550V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2480542	NM_015720.4(PODXL2):c.1763G>C (p.Gly588Ala)	LOC129937492, PODXL2 (G588A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398323	NM_015720.4(PODXL2):c.1612G>A (p.Gly538Ser)	LOC129937491, PODXL2 (G538S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353027	NM_015720.4(PODXL2):c.1782G>T (p.Glu594Asp)	LOC129937492, PODXL2 (E594D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2296724	NM_015720.4(PODXL2):c.1766G>A (p.Gly589Asp)	LOC129937492, PODXL2 (G589D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2265900	NM_015720.4(PODXL2):c.1765G>A (p.Gly589Ser)	LOC129937492, PODXL2 (G589S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance