"PreventionGenetics, part of Exact Sciences"[submitter] AND "MYL3"[gen - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 178086	NM_000258.3(MYL3):c.*9C>T	MYL3	Single nucleotide variant (3 prime UTR variant)	not specified +1 more	GBenign/Likely benign
Select item 263711	NM_000258.3(MYL3):c.477G>A (p.Thr159=)	MYL3	Single nucleotide variant (synonymous variant)	Cardiovascular phenotype +4 more	GLikely benign
Select item 14063	NM_000258.3(MYL3):c.427G>A (p.Glu143Lys)	MYL3 (E143K)	Single nucleotide variant (missense variant)	MYL3-related disorder +6 more	GConflicting classifications of pathogenicity
Select item 227622	NM_000258.3(MYL3):c.420C>T (p.Phe140=)	MYL3	Single nucleotide variant (synonymous variant)	Cardiomyopathy +5 more	GLikely benign
Select item 2629895	NM_000258.3(MYL3):c.349A>C (p.Met117Leu)	MYL3 (M117L +1 more)	Single nucleotide variant (missense variant)	MYL3-related disorder	GUncertain significance
Select item 255638	NM_000258.3(MYL3):c.307+37A>C	MYL3	Single nucleotide variant (intron variant)	Hypertrophic cardiomyopathy 8 +2 more	GBenign
Select item 345570	NM_000258.3(MYL3):c.219C>T (p.Tyr73=)	MYL3	Single nucleotide variant (synonymous variant)	not specified +6 more	GConflicting classifications of pathogenicity
Select item 255637	NM_000258.3(MYL3):c.129+44G>T	MYL3	Single nucleotide variant (intron variant)	not provided +2 more	GBenign
Select item 43129	NM_000258.3(MYL3):c.69C>T (p.Pro23=)	MYL3	Single nucleotide variant (synonymous variant)	not specified +5 more	GBenign
Select item 378219	NM_000258.3(MYL3):c.36T>C (p.Asp12=)	MYL3	Single nucleotide variant (synonymous variant)	not provided +4 more	GLikely benign
Select item 3050528	NM_000258.3(MYL3):c.9C>T (p.Pro3=)	MYL3	Single nucleotide variant (synonymous variant)	MYL3-related disorder +1 more	GLikely benign