CARNMT1[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 782145	NM_152420.3(CARNMT1):c.885T>C (p.Asp295=)	CARNMT1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 3137393	NM_152420.3(CARNMT1):c.857G>T (p.Gly286Val)	CARNMT1 (G207V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3263329	NM_152420.3(CARNMT1):c.748A>C (p.Lys250Gln)	CARNMT1 (K171Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3137391	NM_152420.3(CARNMT1):c.742A>G (p.Ile248Val)	CARNMT1 (I248V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3137390	NM_152420.3(CARNMT1):c.584A>G (p.Glu195Gly)	CARNMT1 (E116G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2532281	NM_152420.3(CARNMT1):c.583G>C (p.Glu195Gln)	CARNMT1 (E195Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2289579	NM_152420.3(CARNMT1):c.366A>G (p.Ile122Met)	CARNMT1 (I122M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3137389	NM_152420.3(CARNMT1):c.364A>G (p.Ile122Val)	CARNMT1 (I43V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2508222	NM_152420.3(CARNMT1):c.324C>A (p.His108Gln)	CARNMT1 (H29Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2245298	NM_152420.3(CARNMT1):c.322C>T (p.His108Tyr)	CARNMT1 (H29Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2616345	NM_152420.3(CARNMT1):c.248G>A (p.Arg83Gln)	CARNMT1 (R4Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance