Related gene-specific medical variations for Gene (Select 256710) - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3281579	NM_001304964.2(GLIPR1L1):c.136G>A (p.Gly46Ser)	CAPS2, GLIPR1L1 (G46S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3100227	NM_001304964.2(GLIPR1L1):c.458T>C (p.Val153Ala)	CAPS2, GLIPR1L1 (V153A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2604109	NM_001304964.2(GLIPR1L1):c.545C>T (p.Pro182Leu)	CAPS2, GLIPR1L1 (P182L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2556360	NM_001304964.2(GLIPR1L1):c.154G>A (p.Ala52Thr)	CAPS2, GLIPR1L1 (A52T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2540365	NM_001304964.2(GLIPR1L1):c.550G>C (p.Val184Leu)	CAPS2, GLIPR1L1 (V184L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2378856	NM_001304964.2(GLIPR1L1):c.230T>C (p.Phe77Ser)	CAPS2, GLIPR1L1 (F77S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2331261	NM_001304964.2(GLIPR1L1):c.523G>A (p.Gly175Arg)	CAPS2, GLIPR1L1 (G175R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2324255	NM_001304964.2(GLIPR1L1):c.182A>G (p.Asp61Gly)	CAPS2, GLIPR1L1 (D61G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2283938	NM_001304964.2(GLIPR1L1):c.404G>A (p.Cys135Tyr)	CAPS2, GLIPR1L1 (C135Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2281603	NM_001304964.2(GLIPR1L1):c.560A>C (p.Glu187Ala)	CAPS2, GLIPR1L1 (E187A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2267921	NM_001304964.2(GLIPR1L1):c.463A>G (p.Met155Val)	CAPS2, GLIPR1L1 (M155V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance