IGFBPL1[gene] and "single gene"[properties] - ClinVar

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Items: 38

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2463719	NM_001007563.3(IGFBPL1):c.830G>A (p.Arg277His)	IGFBPL1 (R277H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 776420	NM_001007563.3(IGFBPL1):c.824_830del (p.Asp275fs)	IGFBPL1 (D275fs)	Deletion (frameshift variant)	not provided	GBenign
Select item 776421	NM_001007563.3(IGFBPL1):c.818_819insA (p.Pro274fs)	IGFBPL1 (P274fs)	Insertion (frameshift variant)	not provided	GBenign
Select item 2371877	NM_001007563.3(IGFBPL1):c.786T>G (p.Asp262Glu)	IGFBPL1 (D262E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3285543	NM_001007563.3(IGFBPL1):c.761C>T (p.Ser254Phe)	IGFBPL1 (S254F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108634	NM_001007563.3(IGFBPL1):c.731A>G (p.His244Arg)	IGFBPL1 (H244R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108633	NM_001007563.3(IGFBPL1):c.701G>A (p.Arg234Gln)	IGFBPL1 (R234Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219357	NM_001007563.3(IGFBPL1):c.693C>A (p.Asn231Lys)	IGFBPL1 (N231K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384326	NM_001007563.3(IGFBPL1):c.682A>G (p.Ile228Val)	IGFBPL1 (I228V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108632	NM_001007563.3(IGFBPL1):c.647G>A (p.Arg216Gln)	IGFBPL1 (R216Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108631	NM_001007563.3(IGFBPL1):c.635C>G (p.Ala212Gly)	IGFBPL1 (A212G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2547748	NM_001007563.3(IGFBPL1):c.631A>T (p.Ile211Leu)	IGFBPL1 (I211L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2261935	NM_001007563.3(IGFBPL1):c.523T>A (p.Ser175Thr)	IGFBPL1 (S175T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108630	NM_001007563.3(IGFBPL1):c.497A>G (p.Asn166Ser)	IGFBPL1 (N166S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108629	NM_001007563.3(IGFBPL1):c.485G>A (p.Arg162Gln)	IGFBPL1 (R162Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108628	NM_001007563.3(IGFBPL1):c.449C>T (p.Pro150Leu)	IGFBPL1 (P150L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2659198	NM_001007563.3(IGFBPL1):c.444C>T (p.Asp148=)	IGFBPL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2485226	NM_001007563.3(IGFBPL1):c.416A>T (p.His139Leu)	IGFBPL1 (H139L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108627	NM_001007563.3(IGFBPL1):c.367C>T (p.Pro123Ser)	IGFBPL1 (P123S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362826	NM_001007563.3(IGFBPL1):c.355G>C (p.Gly119Arg)	IGFBPL1 (G119R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2405492	NM_001007563.3(IGFBPL1):c.343T>C (p.Cys115Arg)	IGFBPL1 (C115R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2280248	NM_001007563.3(IGFBPL1):c.340G>A (p.Val114Ile)	IGFBPL1 (V114I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219482	NM_001007563.3(IGFBPL1):c.319G>A (p.Val107Met)	IGFBPL1 (V107M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357080	NM_001007563.3(IGFBPL1):c.247G>A (p.Gly83Arg)	IGFBPL1 (G83R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2241488	NM_001007563.3(IGFBPL1):c.232G>T (p.Gly78Trp)	IGFBPL1 (G78W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2659199	NM_001007563.3(IGFBPL1):c.208C>T (p.Leu70=)	IGFBPL1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3285542	NM_001007563.3(IGFBPL1):c.203G>A (p.Arg68His)	IGFBPL1 (R68H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2601748	NM_001007563.3(IGFBPL1):c.183C>A (p.Asp61Glu)	IGFBPL1 (D61E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2324931	NM_001007563.3(IGFBPL1):c.176C>G (p.Ala59Gly)	IGFBPL1 (A59G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2332498	NM_001007563.3(IGFBPL1):c.167G>A (p.Gly56Glu)	IGFBPL1 (G56E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396957	NM_001007563.3(IGFBPL1):c.161C>T (p.Ala54Val)	IGFBPL1 (A54V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242598	NM_001007563.3(IGFBPL1):c.151C>T (p.Pro51Ser)	IGFBPL1 (P51S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532977	NM_001007563.3(IGFBPL1):c.133G>A (p.Gly45Ser)	IGFBPL1 (G45S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108625	NM_001007563.3(IGFBPL1):c.130G>A (p.Glu44Lys)	IGFBPL1 (E44K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2326819	NM_001007563.3(IGFBPL1):c.119C>A (p.Pro40Gln)	IGFBPL1 (P40Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108624	NM_001007563.3(IGFBPL1):c.101G>T (p.Arg34Leu)	IGFBPL1 (R34L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3108623	NM_001007563.3(IGFBPL1):c.100C>T (p.Arg34Trp)	IGFBPL1 (R34W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2545714	NM_001007563.3(IGFBPL1):c.74G>A (p.Ser25Asn)	IGFBPL1 (S25N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 38