"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "LOC126859646"[ - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3379638	NM_020442.6(VARS2):c.1787C>T (p.Ala596Val)	LOC126859646, VARS2 (A456V +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 373702	NM_020442.6(VARS2):c.1850C>T (p.Thr617Met)	LOC126859646, VARS2 (T617M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1693907	NM_020442.6(VARS2):c.1955G>A (p.Arg652Gln)	LOC126859646, VARS2 (R512Q +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1929580	NM_020442.6(VARS2):c.2023G>C (p.Gly675Arg)	LOC126859646, VARS2 (G675R +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 380157	NM_020442.6(VARS2):c.2038G>T (p.Val680Leu)	LOC126859646, VARS2 (V680L +2 more)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign
Select item 380159	NM_020442.6(VARS2):c.2186-10T>C	LOC126859646, VARS2	Single nucleotide variant (intron variant)	not provided +2 more	GBenign
Select item 377004	NM_020442.6(VARS2):c.2293G>A (p.Val765Met)	LOC126859646, VARS2 (V765M +2 more)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 380176	NM_020442.6(VARS2):c.2328C>T (p.Ser776=)	LOC126859646, VARS2	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 559215	NM_020442.6(VARS2):c.2330C>T (p.Pro777Leu)	LOC126859646, VARS2 (P777L +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3379639	NM_020442.6(VARS2):c.2339C>T (p.Ala780Val)	LOC126859646, VARS2 (A640V +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance