"Ambry Genetics"[submitter] AND "LOC129938031"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2406929	NM_024871.4(MAP6D1):c.368C>T (p.Ala123Val)	LOC129938031, MAP6D1 (A123V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3293143	NM_024871.4(MAP6D1):c.361G>A (p.Gly121Ser)	LOC129938031, MAP6D1 (G121S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470280	NM_024871.4(MAP6D1):c.356C>G (p.Pro119Arg)	LOC129938031, MAP6D1 (P119R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401202	NM_024871.4(MAP6D1):c.343G>A (p.Val115Ile)	LOC129938031, MAP6D1 (V115I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2302761	NM_024871.4(MAP6D1):c.328C>A (p.Pro110Thr)	LOC129938031, MAP6D1 (P110T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3123137	NM_024871.4(MAP6D1):c.305C>T (p.Ala102Val)	LOC129938031, MAP6D1 (A102V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3293144	NM_024871.4(MAP6D1):c.268G>A (p.Gly90Arg)	LOC129938031, MAP6D1 (G90R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar