Related gene-specific medical variations for Gene (Select 9649) - ClinVar

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Links from Gene

Items: 33

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3294177	NM_012098.3(ANGPTL2):c.188A>T (p.Gln63Leu)	ANGPTL2, RALGPS1 (Q63L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3294166	NM_012098.3(ANGPTL2):c.137G>A (p.Arg46Gln)	ANGPTL2, RALGPS1 (R46Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3294155	NM_012098.3(ANGPTL2):c.256A>G (p.Lys86Glu)	ANGPTL2, RALGPS1 (K86E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3294144	NM_012098.3(ANGPTL2):c.757C>A (p.Pro253Thr)	ANGPTL2, RALGPS1 (P253T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3294133	NM_012098.3(ANGPTL2):c.190C>T (p.Arg64Trp)	ANGPTL2, RALGPS1 (R64W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118586	NM_012098.3(ANGPTL2):c.85G>A (p.Gly29Ser)	ANGPTL2, RALGPS1 (G29S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118578	NM_012098.3(ANGPTL2):c.7C>T (p.Pro3Ser)	ANGPTL2, RALGPS1 (P3S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118567	NM_012098.3(ANGPTL2):c.664C>T (p.Pro222Ser)	ANGPTL2, RALGPS1 (P222S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118547	NM_012098.3(ANGPTL2):c.309C>G (p.Ile103Met)	ANGPTL2, RALGPS1 (I103M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118544	NM_012098.3(ANGPTL2):c.254A>C (p.His85Pro)	ANGPTL2, RALGPS1 (H85P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118521	NM_012098.3(ANGPTL2):c.1237G>A (p.Gly413Ser)	ANGPTL2, RALGPS1 (G413S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118513	NM_012098.3(ANGPTL2):c.101C>T (p.Ser34Leu)	ANGPTL2, RALGPS1 (S34L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2603667	NM_012098.3(ANGPTL2):c.578A>T (p.Gln193Leu)	ANGPTL2, RALGPS1 (Q193L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2600759	NM_012098.3(ANGPTL2):c.1378A>G (p.Ser460Gly)	ANGPTL2, RALGPS1 (S460G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2600410	NM_012098.3(ANGPTL2):c.314C>T (p.Thr105Met)	ANGPTL2, RALGPS1 (T105M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2542990	NM_012098.3(ANGPTL2):c.1267C>T (p.His423Tyr)	ANGPTL2, RALGPS1 (H423Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2526446	NM_012098.3(ANGPTL2):c.775C>T (p.Pro259Ser)	ANGPTL2, RALGPS1 (P259S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2472046	NM_012098.3(ANGPTL2):c.211G>A (p.Val71Ile)	ANGPTL2, RALGPS1 (V71I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2468391	NM_012098.3(ANGPTL2):c.191G>A (p.Arg64Gln)	ANGPTL2, RALGPS1 (R64Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2410992	NM_012098.3(ANGPTL2):c.887C>T (p.Pro296Leu)	ANGPTL2, RALGPS1 (P296L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2387629	NM_012098.3(ANGPTL2):c.193G>A (p.Val65Ile)	ANGPTL2, RALGPS1 (V65I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2384317	NM_012098.3(ANGPTL2):c.1469A>G (p.Asn490Ser)	ANGPTL2, RALGPS1 (N490S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2365657	NM_012098.3(ANGPTL2):c.803C>T (p.Thr268Ile)	ANGPTL2, RALGPS1 (T268I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2331897	NM_012098.3(ANGPTL2):c.76G>A (p.Gly26Ser)	ANGPTL2, RALGPS1 (G26S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2320513	NM_012098.3(ANGPTL2):c.569C>G (p.Ala190Gly)	ANGPTL2, RALGPS1 (A190G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2302110	NM_012098.3(ANGPTL2):c.176T>C (p.Ile59Thr)	ANGPTL2, RALGPS1 (I59T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2289567	NM_012098.3(ANGPTL2):c.445C>T (p.Arg149Trp)	ANGPTL2, RALGPS1 (R149W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2276831	NM_012098.3(ANGPTL2):c.1375C>T (p.Arg459Trp)	ANGPTL2, RALGPS1 (R459W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2256111	NM_012098.3(ANGPTL2):c.343G>A (p.Gly115Ser)	ANGPTL2, RALGPS1 (G115S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2255739	NM_012098.3(ANGPTL2):c.226C>G (p.Pro76Ala)	ANGPTL2, RALGPS1 (P76A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2246682	NM_012098.3(ANGPTL2):c.661C>T (p.Pro221Ser)	ANGPTL2, RALGPS1 (P221S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2230029	NM_012098.3(ANGPTL2):c.901C>T (p.Arg301Cys)	ANGPTL2, RALGPS1 (R301C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2222447	NM_012098.3(ANGPTL2):c.1195C>T (p.Arg399Cys)	ANGPTL2, RALGPS1 (R399C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Links from Gene

Items: 33