"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "VARS2"[gene] - ClinVar

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Items: 44

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 380148	NM_020442.6(VARS2):c.-28+82T>C	VARS2	Single nucleotide variant (synonymous variant +1 more)	not specified +2 more	GBenign
Select item 559214	NM_020442.6(VARS2):c.-27-1G>T	VARS2 (Q21H)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 380149	NM_020442.6(VARS2):c.21C>T (p.Ala7=)	VARS2	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign
Select item 1300565	NM_020442.6(VARS2):c.23C>A (p.Ser8Tyr)	VARS2 (S38Y +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 380188	NM_020442.6(VARS2):c.76C>T (p.His26Tyr)	VARS2 (H26Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GBenign
Select item 380150	NM_020442.6(VARS2):c.168G>T (p.Ala56=)	VARS2	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign
Select item 380189	NM_020442.6(VARS2):c.190G>A (p.Gly64Arg)	VARS2 (G64R +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign
Select item 425368	NM_020442.6(VARS2):c.423G>A (p.Met141Ile)	VARS2 (M141I +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 380151	NM_020442.6(VARS2):c.574-9C>T	VARS2	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 506357	NM_020442.6(VARS2):c.607G>A (p.Gly203Arg)	VARS2 (G203R +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1029206	NM_020442.6(VARS2):c.631C>T (p.Arg211Trp)	VARS2 (R71W +2 more)	Single nucleotide variant (missense variant)	Combined oxidative phosphorylation defect type 20 +1 more	GUncertain significance
Select item 1032686	NM_020442.6(VARS2):c.736T>C (p.Cys246Arg)	VARS2 (C106R +2 more)	Single nucleotide variant (missense variant)	Combined oxidative phosphorylation defect type 20 +1 more	GConflicting classifications of pathogenicity
Select item 2074406	NM_020442.6(VARS2):c.801G>A (p.Ala267=)	VARS2	Single nucleotide variant (synonymous variant)	not provided	GConflicting classifications of pathogenicity
Select item 382467	NM_020442.6(VARS2):c.864G>A (p.Ser288=)	VARS2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 381459	NM_020442.6(VARS2):c.876G>A (p.Val292=)	VARS2	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign/Likely benign
Select item 522814	NM_020442.6(VARS2):c.1168G>A (p.Ala390Thr)	VARS2 (A390T +2 more)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 380152	NM_020442.6(VARS2):c.1272C>T (p.Ser424=)	VARS2	Single nucleotide variant (synonymous variant)	Combined oxidative phosphorylation defect type 20 +2 more	GBenign
Select item 380153	NM_020442.6(VARS2):c.1288C>T (p.Leu430=)	VARS2	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign
Select item 380154	NM_020442.6(VARS2):c.1345T>C (p.Trp449Arg)	VARS2 (W449R +2 more)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign
Select item 380155	NM_020442.6(VARS2):c.1353G>A (p.Leu451=)	VARS2	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1163848	NM_020442.6(VARS2):c.1484T>G (p.Val495Gly)	VARS2 (V355G +2 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 380156	NM_020442.6(VARS2):c.1656T>C (p.Val552=)	VARS2	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign
Select item 1163849	NM_020442.6(VARS2):c.1661G>A (p.Arg554Gln)	VARS2 (R414Q +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 809891	NM_020442.6(VARS2):c.1691C>T (p.Ala564Val)	VARS2 (A424V +2 more)	Single nucleotide variant (missense variant)	not specified +2 more	GConflicting classifications of pathogenicity
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
Select item 1029202	NM_020442.6(VARS2):c.2501G>A (p.Arg834His)	VARS2 (R834H +2 more)	Single nucleotide variant (missense variant)	Combined oxidative phosphorylation defect type 20 +1 more	GUncertain significance
Select item 445608	NM_020442.6(VARS2):c.2551C>T (p.Arg851Cys)	VARS2 (R851C +2 more)	Single nucleotide variant (missense variant)	Combined oxidative phosphorylation defect type 20 +1 more	GConflicting classifications of pathogenicity
Select item 1032682	NM_020442.6(VARS2):c.2624C>T (p.Pro875Leu)	VARS2 (P875L +2 more)	Single nucleotide variant (missense variant)	Combined oxidative phosphorylation defect type 20 +2 more	GUncertain significance
Select item 380160	NM_020442.6(VARS2):c.2658C>T (p.Pro886=)	VARS2	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign
Select item 380161	NM_020442.6(VARS2):c.2750G>A (p.Arg917Gln)	VARS2 (R917Q +2 more)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign
Select item 380162	NM_020442.6(VARS2):c.2893G>A (p.Ala965Thr)	VARS2 (A965T +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 3379640	NM_020442.6(VARS2):c.2924C>T (p.Pro975Leu)	VARS2 (P1005L +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 638479	NM_020442.6(VARS2):c.3020A>G (p.Gln1007Arg)	VARS2 (Q1007R +2 more)	Single nucleotide variant (missense variant)	Combined oxidative phosphorylation defect type 20 +1 more	GUncertain significance
Select item 380163	NM_020442.6(VARS2):c.3033C>T (p.Asp1011=)	VARS2	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 380164	NM_020442.6(VARS2):c.3146G>A (p.Arg1049Gln)	VARS2 (R1049Q +2 more)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign

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Items: 44