Related gene-specific medical variations for Gene (Select 79814) - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3095969	NM_024758.5(AGMAT):c.195G>T (p.Gln65His)	AGMAT, LOC129929491 (Q65H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3095966	NM_024758.5(AGMAT):c.175A>G (p.Met59Val)	AGMAT, LOC129929491 (M59V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3095961	NM_024758.5(AGMAT):c.11T>G (p.Leu4Arg)	AGMAT, LOC129929491 (L4R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597588	NM_024758.5(AGMAT):c.91C>T (p.Arg31Cys)	AGMAT, LOC129929491 (R31C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534153	NM_024758.5(AGMAT):c.220G>T (p.Ala74Ser)	AGMAT, LOC129929491 (A74S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355729	NM_024758.5(AGMAT):c.137G>A (p.Ser46Asn)	AGMAT, LOC129929491 (S46N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2352507	NM_024758.5(AGMAT):c.28G>T (p.Ala10Ser)	AGMAT, LOC129929491 (A10S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319891	NM_024758.5(AGMAT):c.82C>G (p.Pro28Ala)	AGMAT, LOC129929491 (P28A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2238958	NM_024758.5(AGMAT):c.100C>T (p.Arg34Cys)	AGMAT, LOC129929491 (R34C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 784932	NM_024758.5(AGMAT):c.30C>T (p.Ala10=)	AGMAT, LOC129929491	Single nucleotide variant (synonymous variant)	not provided	GLikely benign