"Ambry Genetics"[submitter] AND "CD36"[gene] - ClinVar

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Items: 40

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2528587	NM_001001548.3(CD36):c.43A>C (p.Ile15Leu)	CD36 (I15L)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2370989	NM_001001548.3(CD36):c.52G>A (p.Val18Ile)	CD36 (V18I)	Single nucleotide variant (missense variant +3 more)	not specified	GLikely benign
Select item 2344734	NM_001001548.3(CD36):c.143C>T (p.Thr48Ile)	CD36 (T48I)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2526309	NM_001001548.3(CD36):c.199A>G (p.Ile67Val)	CD36 (I67V)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2607891	NM_001001548.3(CD36):c.202T>G (p.Phe68Val)	CD36 (F68V)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2364548	NM_001001548.3(CD36):c.264A>T (p.Arg88Ser)	CD36 (R12S +2 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2472346	NM_001001548.3(CD36):c.353A>G (p.Asn118Ser)	CD36 (N42S +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2366413	NM_001001548.3(CD36):c.362T>C (p.Ile121Thr)	CD36 (I121T +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2218720	NM_001001548.3(CD36):c.401A>T (p.Asn134Ile)	CD36 (N100I +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2293144	NM_001001548.3(CD36):c.427G>T (p.Ala143Ser)	CD36 (A143S +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3140567	NM_001001548.3(CD36):c.523T>G (p.Leu175Val)	CD36 (L141V +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 2541822	NM_001001548.3(CD36):c.553C>A (p.Pro185Thr)	CD36 (P109T +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2257561	NM_001001548.3(CD36):c.580G>T (p.Val194Phe)	CD36 (V118F +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2556301	NM_001001548.3(CD36):c.623C>A (p.Ala208Glu)	CD36 (A174E +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3140569	NM_001001548.3(CD36):c.625G>T (p.Asp209Tyr)	CD36 (D209Y +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 911919	NM_001001548.3(CD36):c.625G>C (p.Asp209His)	CD36 (D133H +4 more)	Single nucleotide variant (missense variant +1 more)	Platelet-type bleeding disorder 10 +1 more	GUncertain significance
Select item 360761	NM_001001548.3(CD36):c.649G>A (p.Gly217Arg)	CD36 (G217R +4 more)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 911920	NM_001001548.3(CD36):c.655G>T (p.Asp219Tyr)	CD36 (D159Y +4 more)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GUncertain significance
Select item 2244807	NM_001001548.3(CD36):c.670G>T (p.Val224Phe)	CD36 (V148F +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 360762	NM_001001548.3(CD36):c.682G>A (p.Asp228Asn)	CD36 (D228N +4 more)	Single nucleotide variant (missense variant +1 more)	Platelet-type bleeding disorder 10 +1 more	GUncertain significance
Select item 3264825	NM_001001548.3(CD36):c.707T>G (p.Leu236Arg)	CD36 (L236R +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3264824	NM_001001548.3(CD36):c.730G>A (p.Asp244Asn)	CD36 (D168N +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3140571	NM_001001548.3(CD36):c.745A>G (p.Thr249Ala)	CD36 (T173A +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3140572	NM_001001548.3(CD36):c.785A>C (p.Gln262Pro)	CD36 (Q186P +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3140573	NM_001001548.3(CD36):c.806C>T (p.Ser269Phe)	CD36 (S114F +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2406311	NM_001001548.3(CD36):c.832G>C (p.Val278Leu)	CD36 (V202L +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381464	NM_001001548.3(CD36):c.880G>C (p.Val294Leu)	CD36 (V139L +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140574	NM_001001548.3(CD36):c.901G>A (p.Ala301Thr)	CD36 (A241T +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3264826	NM_001001548.3(CD36):c.962A>G (p.Asn321Ser)	CD36 (N321S +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222770	NM_001001548.3(CD36):c.976G>T (p.Gly326Cys)	CD36 (G171C +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2280228	NM_001001548.3(CD36):c.979G>A (p.Val327Met)	CD36 (V251M +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 360764	NM_001001548.3(CD36):c.1000A>G (p.Lys334Glu)	CD36 (K334E +5 more)	Single nucleotide variant (missense variant)	Platelet-type bleeding disorder 10 +2 more	GUncertain significance
Select item 2208360	NM_001001548.3(CD36):c.1013C>T (p.Pro338Leu)	CD36 (P262L +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2405387	NM_001001548.3(CD36):c.1030C>T (p.Pro344Ser)	CD36 (P305S +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3140564	NM_001001548.3(CD36):c.1126A>G (p.Ile376Val)	CD36 (I300V +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2494965	NM_001001548.3(CD36):c.1145A>C (p.Gln382Pro)	CD36 (Q382P +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3140565	NM_001001548.3(CD36):c.1231G>A (p.Val411Met)	CD36 (V351M +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 360770	NM_001001548.3(CD36):c.1279G>T (p.Ala427Ser)	CD36 (A427S +5 more)	Single nucleotide variant (missense variant +1 more)	Platelet-type bleeding disorder 10 +2 more	GConflicting classifications of pathogenicity
Select item 3140566	NM_001001548.3(CD36):c.1283A>G (p.Asn428Ser)	CD36 (N389S +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2606350	NM_001001548.3(CD36):c.1324G>C (p.Gly442Arg)	CD36 (G408R +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 40