"PreventionGenetics, part of Exact Sciences"[submitter] AND "CD36"[gen - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3030684	NM_001001548.3(CD36):c.120+399TG[8]	CD36	Microsatellite (intron variant)	CD36-related disorder	GLikely benign
Select item 3041737	NM_001001548.3(CD36):c.157_158delinsG (p.Asn53fs)	CD36 (N53fs)	Indel (frameshift variant +3 more)	CD36-related disorder	GLikely pathogenic
Select item 1302901	NM_001001548.3(CD36):c.338_339del (p.Ser113fs)	CD36 (S113fs +2 more)	Microsatellite (frameshift variant +2 more)	CD36-related disorder +1 more	GUncertain significance
Select item 3029091	NM_001001548.3(CD36):c.378_381dup (p.Val128fs)	CD36 (V128fs +2 more)	Duplication (frameshift variant +2 more)	CD36-related disorder	GLikely pathogenic
Select item 909794	NM_001001548.3(CD36):c.403T>C (p.Phe135Leu)	CD36 (F59L +2 more)	Single nucleotide variant (missense variant +2 more)	Platelet-type bleeding disorder 10 +1 more	GConflicting classifications of pathogenicity
Select item 1708388	NM_001001548.3(CD36):c.443T>A (p.Ile148Asn)	CD36 (I114N +2 more)	Single nucleotide variant (missense variant +3 more)	CD36-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 3061735	NM_001001548.3(CD36):c.534G>C (p.Leu178=)	CD36	Single nucleotide variant (synonymous variant +2 more)	CD36-related disorder	GLikely benign
Select item 810108	NM_001001548.3(CD36):c.550G>A (p.Asp184Asn)	CD36 (D150N +3 more)	Single nucleotide variant (missense variant +2 more)	Platelet-type bleeding disorder 10 +2 more	GConflicting classifications of pathogenicity
Select item 908989	NM_001001548.3(CD36):c.819-8G>A	CD36	Single nucleotide variant (intron variant)	Platelet-type bleeding disorder 10 +1 more	GConflicting classifications of pathogenicity
Select item 908992	NM_001001548.3(CD36):c.875G>T (p.Arg292Ile)	CD36 (R232I +5 more)	Single nucleotide variant (missense variant)	Platelet-type bleeding disorder 10 +2 more	GUncertain significance
Select item 3051761	NM_001001548.3(CD36):c.1026A>G (p.Ser342=)	CD36	Single nucleotide variant (synonymous variant +1 more)	CD36-related disorder	GLikely benign
Select item 3036442	NM_001001548.3(CD36):c.1047_1051dup (p.Pro351fs)	CD36 (P196fs +5 more)	Duplication (frameshift variant +1 more)	CD36-related disorder	GLikely pathogenic
Select item 3030004	NM_001001548.3(CD36):c.1077A>G (p.Gly359=)	CD36	Single nucleotide variant (synonymous variant +1 more)	CD36-related disorder	GLikely benign
Select item 3061727	NM_001001548.3(CD36):c.1101T>C (p.His367=)	CD36	Single nucleotide variant (synonymous variant +1 more)	CD36-related disorder	GLikely benign
Select item 2631819	NM_001001548.3(CD36):c.1150_1152delinsCC (p.Ala384fs)	CD36 (A229fs +5 more)	Indel (frameshift variant +1 more)	CD36-related disorder	GLikely pathogenic
Select item 3049270	NM_001001548.3(CD36):c.1152A>C (p.Ala384=)	CD36	Single nucleotide variant (synonymous variant +1 more)	CD36-related disorder	GLikely benign
Select item 632510	NM_001001548.3(CD36):c.1156C>T (p.Arg386Trp)	CD36 (R386W +5 more)	Single nucleotide variant (missense variant +1 more)	CD36-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 3058539	NM_001001548.3(CD36):c.1200-8T>C	CD36	Single nucleotide variant (intron variant)	CD36-related disorder	GLikely benign
Select item 2630063	NM_001001548.3(CD36):c.1200-7_1208del	CD36	Deletion (splice acceptor variant)	CD36-related disorder	GLikely pathogenic
Select item 2636233	NM_001001548.3(CD36):c.1236del (p.Ile413fs)	CD36 (I258fs +5 more)	Deletion (frameshift variant +1 more)	CD36-related disorder	GLikely pathogenic
Select item 417926	NM_001001548.3(CD36):c.1254+1G>A	CD36	Single nucleotide variant (splice donor variant)	Platelet-type bleeding disorder 10 +1 more	GConflicting classifications of pathogenicity
Select item 2634110	NM_001001548.3(CD36):c.1255-1G>C	CD36	Single nucleotide variant (splice acceptor variant)	CD36-related disorder	GLikely pathogenic
Select item 2636824	NM_001001548.3(CD36):c.1348_1353del (p.Ser450_Val451del)	CD36	Deletion (inframe_deletion +1 more)	CD36-related disorder	GUncertain significance
Select item 731329	NM_001001548.3(CD36):c.1404G>A (p.Ser468=)	CD36	Single nucleotide variant (synonymous variant +1 more)	CD36-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 910756	NM_001001548.3(CD36):c.1409C>T (p.Thr470Ile)	CD36 (T410I +5 more)	Single nucleotide variant (missense variant +1 more)	Platelet-type bleeding disorder 10 +1 more	GUncertain significance

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Items: 25