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

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3294285	NM_002402.4(MEST):c.28A>G (p.Met10Val)	MEST (M10V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3125395	NM_002402.4(MEST):c.32G>A (p.Arg11Lys)	MEST (R11K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3125396	NM_002402.4(MEST):c.82T>C (p.Tyr28His)	MEST (Y19H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2247586	NM_002402.4(MEST):c.166C>G (p.Arg56Gly)	MEST (R56G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3125394	NM_002402.4(MEST):c.281T>G (p.Leu94Trp)	MEST (L80W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489503	NM_002402.4(MEST):c.394C>T (p.Arg132Trp)	MEST (R123W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2275659	NM_002402.4(MEST):c.412A>T (p.Asn138Tyr)	MEST (N129Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2368745	NM_002402.4(MEST):c.452T>C (p.Ile151Thr)	MEST (I151T +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2396182	NM_002402.4(MEST):c.466C>A (p.Leu156Ile)	MEST (L147I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381771	NM_002402.4(MEST):c.557G>A (p.Arg186His)	MEST (R172H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2252360	NM_002402.4(MEST):c.658G>A (p.Val220Ile)	MEST (V206I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2386466	NM_002402.4(MEST):c.663T>G (p.Phe221Leu)	MEST (F212L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2526176	NM_002402.4(MEST):c.767A>G (p.Asn256Ser)	MEST (N247S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390261	NM_002402.4(MEST):c.874T>C (p.Phe292Leu)	MEST (F283L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304554	NM_002402.4(MEST):c.908C>G (p.Ser303Cys)	LOC126860176, MEST (S260C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance