senecio greenway - ClinVar - NCBI

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Items: 11

The following term was not found in ClinVar: senecio.
Showing results for Senecio greenwayi. Your search for Senecio greenwayi retrieved no results.

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1687095	NM_207163.3(LMOD2):c.1243_1244del (p.Leu415fs)	LMOD2 (L415fs)	Microsatellite (frameshift variant)	Cardiomyopathy, dilated, 2G	GPathogenic
Select item 1687096	NM_207163.3(LMOD2):c.1537C>T (p.Arg513Ter)	LMOD2	Single nucleotide variant (nonsense)	Cardiomyopathy, dilated, 2G	GPathogenic
Select item 18073	NM_001097577.3(ANG):c.107A>T (p.Gln36Leu)	ANG, EGILA +1 more (Q36L)	Single nucleotide variant (non-coding transcript variant +2 more)	Amyotrophic lateral sclerosis type 9	GPathogenic
Select item 18075	NM_001097577.3(ANG):c.121A>G (p.Lys41Glu)	ANG, EGILA +1 more (K41E)	Single nucleotide variant (non-coding transcript variant +2 more)	Amyotrophic lateral sclerosis type 9	GPathogenic
Select item 18074	NM_001097577.3(ANG):c.122A>T (p.Lys41Ile)	ANG, EGILA +1 more (K41I)	Single nucleotide variant (non-coding transcript variant +2 more)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 18076	NM_001097577.3(ANG):c.164G>A (p.Arg55Lys)	ANG, EGILA +1 more (R55K)	Single nucleotide variant (non-coding transcript variant +2 more)	Amyotrophic lateral sclerosis type 9	GPathogenic
Select item 18077	NM_001097577.3(ANG):c.189C>G (p.Cys63Trp)	ANG, EGILA +1 more (C63W)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 9	GPathogenic
Select item 18078	NM_001097577.3(ANG):c.191A>T (p.Lys64Ile)	ANG, EGILA +1 more (K64I)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 9	GPathogenic
Select item 18079	NM_001097577.3(ANG):c.208A>G (p.Ile70Val)	ANG, EGILA +1 more (I70V)	Single nucleotide variant (missense variant +1 more)	Amyotrophic lateral sclerosis type 9 +2 more	GConflicting classifications of pathogenicity
Select item 164378	NM_000257.4(MYH7):c.1157A>G (p.Tyr386Cys)	MYH7 (Y386C)	Single nucleotide variant (missense variant)	Cardiomyopathy	GLikely pathogenic FDA Recognized database
Select item 517203	NM_005159.5(ACTC1):c.532A>T (p.Met178Leu)	ACTC1, GJD2-DT (M178L)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 11 +5 more	GUncertain significance