"Color Diagnostics, LLC DBA Color Health"[submitter] AND "LOC130057222 - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 628684	NM_001018005.2(TPM1):c.240+4488A>G	LOC130057222, TPM1 +1 more (D22G)	Single nucleotide variant (non-coding transcript variant +2 more)	Cardiomyopathy	GLikely benign
Select item 629720	NM_001018005.2(TPM1):c.240+4545T>C	LOC130057222, TPM1 +1 more (L41P)	Single nucleotide variant (missense variant +1 more)	Cardiomyopathy	GLikely benign