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

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3049619	NM_006440.5(TXNRD2):c.24G>C (p.Leu8=)	COMT, TXNRD2	Single nucleotide variant (synonymous variant +2 more)	TXNRD2-related disorder	GLikely benign
Select item 3046825	NM_000754.4(COMT):c.1-5T>C	COMT	Single nucleotide variant (5 prime UTR variant +1 more)	COMT-related disorder	GLikely benign
Select item 256785	NM_000754.4(COMT):c.186C>T (p.His62=)	COMT	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign
Select item 3046309	NM_000754.4(COMT):c.207C>T (p.Pro69=)	COMT	Single nucleotide variant (synonymous variant)	COMT-related disorder	GLikely benign
Select item 722444	NM_000754.4(COMT):c.289+9C>T	COMT	Single nucleotide variant (intron variant)	COMT-related disorder +1 more	GBenign/Likely benign
Select item 256786	NM_000754.4(COMT):c.408C>G (p.Leu136=)	COMT	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign
Select item 790230	NM_000754.4(COMT):c.438C>T (p.Ala146=)	COMT	Single nucleotide variant (synonymous variant)	COMT-related disorder +1 more	GBenign
Select item 17591	NM_000754.4(COMT):c.472G>A (p.Val158Met)	COMT (V158M +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign
Select item 3045453	NM_000754.4(COMT):c.756G>A (p.Glu252=)	ARVCF, COMT	Single nucleotide variant (synonymous variant)	COMT-related disorder	GLikely benign
Select item 3054100	NM_000754.4(COMT):c.801C>T (p.Ser267=)	ARVCF, COMT	Single nucleotide variant (synonymous variant)	COMT-related disorder	GLikely benign
Select item 256784	NM_000754.4(COMT):c.*10dup	ARVCF, COMT	Duplication (3 prime UTR variant)	not specified +1 more	GBenign