C3714995[trait identifier] AND "Genome Diagnostics Laboratory, Univers - ClinVar

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Items: 26

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 382816	NM_032578.4(MYPN):c.660G>A (p.Arg220=)	MYPN	Single nucleotide variant (synonymous variant +2 more)	not specified +2 more	GBenign/Likely benign
Select item 227722	NM_032578.4(MYPN):c.734C>G (p.Ala245Gly)	MYPN (A245G)	Single nucleotide variant (missense variant +2 more)	Dilated cardiomyopathy 1KK +3 more	GLikely benign
Select item 31836	NM_032578.4(MYPN):c.1104C>T (p.Gly368=)	MYPN	Single nucleotide variant (synonymous variant +1 more)	Cardiovascular phenotype +3 more	GBenign/Likely benign
Select item 191749	NM_032578.4(MYPN):c.1130G>A (p.Arg377Gln)	MYPN (R377Q +1 more)	Single nucleotide variant (missense variant +1 more)	Cardiovascular phenotype +4 more	GConflicting classifications of pathogenicity
Select item 138415	NM_032578.4(MYPN):c.1134C>T (p.Ile378=)	MYPN	Single nucleotide variant (synonymous variant +1 more)	not specified +3 more	GBenign/Likely benign
Select item 477737	NM_032578.4(MYPN):c.1236C>A (p.Thr412=)	MYPN	Single nucleotide variant (synonymous variant +1 more)	Dilated cardiomyopathy 1KK +3 more	GBenign/Likely benign
Select item 201869	NM_032578.4(MYPN):c.1246-19G>A	MYPN	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1KK +1 more	GBenign
Select item 31827	NM_032578.4(MYPN):c.1399G>A (p.Glu467Lys)	MYPN (E467K +1 more)	Single nucleotide variant (missense variant +1 more)	Cardiovascular phenotype +3 more	GBenign
Select item 227714	NM_032578.4(MYPN):c.1460-14T>A	MYPN	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1KK +3 more	GBenign/Likely benign
Select item 522235	NM_032578.4(MYPN):c.1593C>T (p.His531=)	MYPN	Single nucleotide variant (synonymous variant +1 more)	Cardiovascular phenotype +1 more	GLikely benign
Select item 522236	NM_032578.4(MYPN):c.1600+21G>C	MYPN	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 31802	NM_032578.4(MYPN):c.1662A>C (p.Ala554=)	MYPN	Single nucleotide variant (synonymous variant +1 more)	not specified +3 more	GBenign/Likely benign
Select item 31805	NM_032578.4(MYPN):c.1935C>T (p.Pro645=)	MYPN	Single nucleotide variant (synonymous variant +1 more)	not provided +3 more	GBenign/Likely benign
Select item 31809	NM_032578.4(MYPN):c.2410G>A (p.Gly804Arg)	MYPN (G804R +1 more)	Single nucleotide variant (missense variant +1 more)	Cardiovascular phenotype +3 more	GBenign/Likely benign
Select item 138418	NM_032578.4(MYPN):c.2447C>T (p.Pro816Leu)	MYPN (P816L +1 more)	Single nucleotide variant (missense variant +1 more)	Dilated cardiomyopathy 1KK +3 more	GBenign/Likely benign
Select item 31831	NM_032578.4(MYPN):c.2864G>A (p.Arg955Gln)	MYPN (R955Q +1 more)	Single nucleotide variant (missense variant +1 more)	MYPN-related myopathy +2 more	GUncertain significance
Select item 227718	NM_032578.4(MYPN):c.2880T>G (p.Ser960=)	MYPN	Single nucleotide variant (synonymous variant +1 more)	Dilated cardiomyopathy 1KK +2 more	GBenign/Likely benign
Select item 138422	NM_032578.4(MYPN):c.2925+9G>C	MYPN	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1KK +2 more	GBenign
Select item 138423	NM_032578.4(MYPN):c.3078G>A (p.Gly1026=)	MYPN	Single nucleotide variant (synonymous variant +1 more)	Dilated cardiomyopathy 1KK +3 more	GBenign
Select item 155824	NM_032578.4(MYPN):c.3124C>T (p.Arg1042Cys)	MYPN (R1042C +1 more)	Single nucleotide variant (missense variant +1 more)	Dilated cardiomyopathy 1KK +3 more	GConflicting classifications of pathogenicity
Select item 31791	NM_032578.4(MYPN):c.3335C>T (p.Pro1112Leu)	MYPN (P1112L +1 more)	Single nucleotide variant (missense variant +1 more)	Cardiomyopathy +6 more	GConflicting classifications of pathogenicity
Select item 389664	NM_032578.4(MYPN):c.3417C>G (p.Arg1139=)	MYPN	Single nucleotide variant (synonymous variant +1 more)	Dilated cardiomyopathy 1KK +3 more	GBenign/Likely benign
Select item 31819	NM_032578.4(MYPN):c.3481C>A (p.Leu1161Ile)	MYPN (L1161I +1 more)	Single nucleotide variant (missense variant +1 more)	Cardiomyopathy +7 more	GConflicting classifications of pathogenicity
Select item 31792	NM_032578.4(MYPN):c.3583G>A (p.Val1195Met)	MYPN (V1195M +1 more)	Single nucleotide variant (missense variant +1 more)	Cardiovascular phenotype +4 more	GConflicting classifications of pathogenicity
Select item 477758	NM_032578.4(MYPN):c.3720C>T (p.Asp1240=)	MYPN	Single nucleotide variant (synonymous variant +1 more)	Dilated cardiomyopathy 1KK +1 more	GLikely benign
Select item 477760	NM_032578.4(MYPN):c.3792C>T (p.Tyr1264=)	MYPN	Single nucleotide variant (synonymous variant +1 more)	Cardiovascular phenotype +3 more	GBenign/Likely benign

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Items: 26