"Ambry Genetics"[submitter] AND "LOC124902806"[gene] - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2340886	NM_198474.4(OLFML1):c.499G>T (p.Asp167Tyr)	LOC124902806, OLFML1 (D167Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204217	NM_198474.4(OLFML1):c.535A>T (p.Ile179Phe)	LOC124902806, OLFML1 (I179F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348567	NM_198474.4(OLFML1):c.581C>T (p.Ala194Val)	LOC124902806, OLFML1 (A58V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2493784	NM_198474.4(OLFML1):c.683A>G (p.His228Arg)	LOC124902806, OLFML1 (H228R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204218	NM_198474.4(OLFML1):c.691G>A (p.Ala231Thr)	LOC124902806, OLFML1 (A95T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204219	NM_198474.4(OLFML1):c.695C>T (p.Thr232Ile)	LOC124902806, OLFML1 (T232I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204220	NM_198474.4(OLFML1):c.778T>A (p.Leu260Met)	LOC124902806, OLFML1 (L124M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2392093	NM_198474.4(OLFML1):c.805T>A (p.Tyr269Asn)	LOC124902806, OLFML1 (Y133N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3204221	NM_198474.4(OLFML1):c.809T>C (p.Ile270Thr)	LOC124902806, OLFML1 (I134T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364183	NM_198474.4(OLFML1):c.848A>G (p.His283Arg)	LOC124902806, OLFML1 (H147R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2604512	NM_198474.4(OLFML1):c.863C>G (p.Thr288Ser)	LOC124902806, OLFML1 (T152S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270375	NM_198474.4(OLFML1):c.896C>T (p.Pro299Leu)	LOC124902806, OLFML1 (P163L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2262866	NM_198474.4(OLFML1):c.994A>G (p.Ser332Gly)	LOC124902806, OLFML1 (S332G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535241	NM_198474.4(OLFML1):c.1102C>T (p.His368Tyr)	LOC124902806, OLFML1 (H232Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2593138	NM_198474.4(OLFML1):c.1155A>C (p.Glu385Asp)	LOC124902806, OLFML1 (E249D +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign