"Ambry Genetics"[submitter] AND "GLIPR1L2"[gene] - ClinVar

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Items: 26

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2520282	NM_001270396.2(GLIPR1L2):c.17C>A (p.Pro6His)	GLIPR1L2 (P6H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3100231	NM_001270396.2(GLIPR1L2):c.26G>C (p.Arg9Pro)	GLIPR1L2 (R9P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2324135	NM_001270396.2(GLIPR1L2):c.37G>T (p.Ala13Ser)	GLIPR1L2 (A13S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2406071	NM_001270396.2(GLIPR1L2):c.38C>T (p.Ala13Val)	GLIPR1L2 (A13V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2614238	NM_001270396.2(GLIPR1L2):c.43T>G (p.Ser15Ala)	GLIPR1L2 (S15A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2591093	NM_001270396.2(GLIPR1L2):c.50C>A (p.Pro17His)	GLIPR1L2 (P17H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2232802	NM_001270396.2(GLIPR1L2):c.65G>T (p.Gly22Val)	GLIPR1L2 (G22V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2603790	NM_001270396.2(GLIPR1L2):c.113C>G (p.Ser38Cys)	GLIPR1L2 (S38C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2542601	NM_001270396.2(GLIPR1L2):c.182A>C (p.His61Pro)	GLIPR1L2 (H61P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2347583	NM_001270396.2(GLIPR1L2):c.217T>C (p.Ser73Pro)	GLIPR1L2 (S73P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3100228	NM_001270396.2(GLIPR1L2):c.232A>T (p.Met78Leu)	GLIPR1L2 (M78L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3100229	NM_001270396.2(GLIPR1L2):c.248C>T (p.Ala83Val)	GLIPR1L2 (A83V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3100230	NM_001270396.2(GLIPR1L2):c.256C>T (p.Arg86Trp)	GLIPR1L2 (R86W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3100232	NM_001270396.2(GLIPR1L2):c.278A>G (p.Lys93Arg)	GLIPR1L2 (K93R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2364698	NM_001270396.2(GLIPR1L2):c.334A>G (p.Lys112Glu)	GLIPR1L2 (K112E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3100233	NM_001270396.2(GLIPR1L2):c.339T>A (p.Phe113Leu)	GLIPR1L2 (F113L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2526968	NM_001270396.2(GLIPR1L2):c.360G>A (p.Met120Ile)	GLIPR1L2 (M120I)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2491118	NM_001270396.2(GLIPR1L2):c.407G>T (p.Ser136Ile)	GLIPR1L2 (S136I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2543220	NM_001270396.2(GLIPR1L2):c.457G>A (p.Gly153Arg)	GLIPR1L2 (G153R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2534165	NM_001270396.2(GLIPR1L2):c.489G>T (p.Trp163Cys)	GLIPR1L2 (W163C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3100235	NM_001270396.2(GLIPR1L2):c.521C>T (p.Thr174Ile)	GLIPR1L2 (T174I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3100236	NM_001270396.2(GLIPR1L2):c.572A>G (p.Asn191Ser)	GLIPR1L2 (N191S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2353165	NM_001270396.2(GLIPR1L2):c.578C>T (p.Ala193Val)	GLIPR1L2 (A193V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2400102	NM_001270396.2(GLIPR1L2):c.670+22T>A	GLIPR1L2 (M231K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2311899	NM_001270396.2(GLIPR1L2):c.670+35T>G	GLIPR1L2 (H235Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3100237	NM_001270396.2(GLIPR1L2):c.670+39G>A	GLIPR1L2 (G237R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 26