"Baylor Genetics"[submitter] AND "LOC126806710"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1032596	NM_198271.5(LMOD3):c.166G>A (p.Asp56Asn)	LMOD3, LOC126806710 (D56N)	Single nucleotide variant (missense variant)	Nemaline myopathy 10	GUncertain significance
Select item 1032594	NM_198271.5(LMOD3):c.127G>A (p.Ala43Thr)	LMOD3, LOC126806710 (A43T)	Single nucleotide variant (missense variant)	Nemaline myopathy 10	GUncertain significance
Select item 1027923	NM_198271.5(LMOD3):c.23C>G (p.Ser8Ter)	LMOD3, LOC126806710 (S8*)	Single nucleotide variant (nonsense)	Nemaline myopathy 10	GLikely pathogenic

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