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

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2616744	NM_002451.4(MTAP):c.14C>T (p.Thr5Ile)	MTAP (T5I)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3213308	NM_002451.4(MTAP):c.86G>A (p.Arg29Lys)	MTAP (R29K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2511529	NM_002451.4(MTAP):c.116G>T (p.Gly39Val)	MTAP (G39V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2207410	NM_002451.4(MTAP):c.118A>C (p.Lys40Gln)	MTAP (K40Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2257112	NM_002451.4(MTAP):c.227C>T (p.Ala76Val)	MTAP (A93V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1319954	NM_002451.4(MTAP):c.278C>T (p.Thr93Ile)	MTAP (T93I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225526	NM_002451.4(MTAP):c.428C>T (p.Pro143Leu)	MTAP (P160L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2512440	NM_002451.4(MTAP):c.475C>G (p.Leu159Val)	MTAP (L159V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2546210	NM_002451.4(MTAP):c.526C>T (p.Arg176Cys)	MTAP (R176C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2623655	NM_002451.4(MTAP):c.670T>C (p.Trp224Arg)	MTAP (W224R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2282856	NM_002451.4(MTAP):c.682G>A (p.Glu228Lys)	MTAP (E228K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3213296	NM_002451.4(MTAP):c.703C>T (p.Arg235Trp)	MTAP (R235W +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3213299	NM_002451.4(MTAP):c.704G>A (p.Arg235Gln)	MTAP (R235Q +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3296515	NM_002451.4(MTAP):c.730G>A (p.Ala244Thr)	MTAP (A244T +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2229359	NM_002451.4(MTAP):c.770A>G (p.Gln257Arg)	MTAP (Q274R +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 914527	NM_002451.4(MTAP):c.788G>T (p.Trp263Leu)	MTAP (W263L)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity