Related gene-specific medical variations for Gene (Select 27244) - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Links from Gene

Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3160543	NM_014454.3(SESN1):c.953A>G (p.Asn318Ser)	ARMC2, SESN1 (N259S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3160542	NM_014454.3(SESN1):c.767C>T (p.Ala256Val)	ARMC2, SESN1 (A197V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3160540	NM_014454.3(SESN1):c.644A>G (p.Asn215Ser)	ARMC2, SESN1 (N215S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3160539	NM_014454.3(SESN1):c.632A>G (p.Asn211Ser)	ARMC2, SESN1 (N86S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3160538	NM_014454.3(SESN1):c.618C>A (p.Asp206Glu)	ARMC2, SESN1 (D81E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3160537	NM_014454.3(SESN1):c.587A>G (p.His196Arg)	ARMC2, SESN1 (H196R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3160536	NM_014454.3(SESN1):c.327A>T (p.Arg109Ser)	ARMC2, SESN1 (R109S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3160535	NM_014454.3(SESN1):c.1592T>C (p.Ile531Thr)	ARMC2, SESN1 (I472T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3160534	NM_014454.3(SESN1):c.1492A>C (p.Thr498Pro)	ARMC2, SESN1 (T373P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3160533	NM_014454.3(SESN1):c.1280A>T (p.Tyr427Phe)	ARMC2, SESN1 (Y368F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2545537	NM_014454.3(SESN1):c.1360G>C (p.Asp454His)	ARMC2, SESN1 (D329H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513295	NM_014454.3(SESN1):c.1216C>G (p.Pro406Ala)	ARMC2, SESN1 (P281A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488389	NM_014454.3(SESN1):c.416G>A (p.Arg139His)	ARMC2, SESN1 (R80H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383465	NM_014454.3(SESN1):c.536T>C (p.Ile179Thr)	ARMC2, SESN1 (I120T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2339613	NM_014454.3(SESN1):c.743C>T (p.Ala248Val)	ARMC2, SESN1 (A123V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2315886	NM_014454.3(SESN1):c.286G>C (p.Gly96Arg)	ARMC2, SESN1 (G37R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2311922	NM_014454.3(SESN1):c.1442A>G (p.Tyr481Cys)	ARMC2, SESN1 (Y356C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2226332	NM_014454.3(SESN1):c.1535A>G (p.Asp512Gly)	ARMC2, SESN1 (D453G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance