"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "LOC126861897"[ - ClinVar - NCBI

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Items: 7

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3380178	NM_000257.4(MYH7):c.5303A>G (p.Glu1768Gly)	LOC126861897, MYH7 (E1768G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 14118	NM_000257.4(MYH7):c.5134C>T (p.Arg1712Trp)	LOC126861897, MHRT +1 more (R1712W)	Single nucleotide variant (non-coding transcript variant +1 more)	Hypertrophic cardiomyopathy	GLikely pathogenic FDA Recognized database
Select item 583204	NM_000257.4(MYH7):c.5011A>G (p.Ile1671Val)	LOC126861897, MHRT +1 more (I1671V)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 218434	NM_000257.4(MYH7):c.4915G>A (p.Ala1639Thr)	LOC126861897, MHRT +1 more (A1639T)	Single nucleotide variant (non-coding transcript variant +1 more)	Hypertrophic cardiomyopathy +4 more	GUncertain significance
Select item 924864	NM_000257.4(MYH7):c.4894G>A (p.Ala1632Thr)	LOC126861897, MHRT +1 more (A1632T)	Single nucleotide variant (non-coding transcript variant +1 more)	Hypertrophic cardiomyopathy +10 more	GUncertain significance
Select item 927894	NM_000257.4(MYH7):c.4819A>G (p.Ser1607Gly)	LOC126861897, MHRT +1 more (S1607G)	Single nucleotide variant (non-coding transcript variant +1 more)	Dilated cardiomyopathy 1S +7 more	GUncertain significance
Select item 924382	NM_000257.4(MYH7):c.4774C>T (p.Arg1592Trp)	LOC126861897, MHRT +1 more (R1592W)	Single nucleotide variant (non-coding transcript variant +1 more)	Hypertrophic cardiomyopathy +2 more	GUncertain significance