ANXA13[gene] and "single gene"[properties] - ClinVar

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Items: 32

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2376441	NM_004306.4(ANXA13):c.938C>T (p.Ala313Val)	ANXA13 (A313V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3299552	NM_004306.4(ANXA13):c.913G>A (p.Gly305Arg)	ANXA13 (G305R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3127266	NM_004306.4(ANXA13):c.890A>C (p.Asp297Ala)	ANXA13 (D338A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2557363	NM_004306.4(ANXA13):c.876G>T (p.Gln292His)	ANXA13 (Q292H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2388461	NM_004306.4(ANXA13):c.691G>A (p.Asp231Asn)	ANXA13 (D272N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2341567	NM_004306.4(ANXA13):c.590T>C (p.Leu197Pro)	ANXA13 (L197P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2249574	NM_004306.4(ANXA13):c.590T>G (p.Leu197Arg)	ANXA13 (L238R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495940	NM_004306.4(ANXA13):c.581A>G (p.Asn194Ser)	ANXA13 (N194S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2230048	NM_004306.4(ANXA13):c.532C>A (p.Leu178Met)	ANXA13 (L178M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3127269	NM_004306.4(ANXA13):c.430A>T (p.Thr144Ser)	ANXA13 (T144S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462068	NM_004306.4(ANXA13):c.409G>A (p.Glu137Lys)	ANXA13 (E137K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2568922	NM_004306.4(ANXA13):c.379G>A (p.Ala127Thr)	ANXA13 (A168T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325052	NM_004306.4(ANXA13):c.356A>C (p.Lys119Thr)	ANXA13 (K119T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3299583	NM_004306.4(ANXA13):c.344C>T (p.Thr115Met)	ANXA13 (T115M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3299572	NM_004306.4(ANXA13):c.343A>C (p.Thr115Pro)	ANXA13 (T156P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2316940	NM_004306.4(ANXA13):c.296T>C (p.Met99Thr)	ANXA13 (M99T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364125	NM_004306.4(ANXA13):c.265G>A (p.Glu89Lys)	ANXA13 (E130K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2544148	NM_004306.4(ANXA13):c.239C>T (p.Ala80Val)	ANXA13 (A80V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3127267	NM_004306.4(ANXA13):c.209G>A (p.Ser70Asn)	ANXA13 (S111N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489347	NM_004306.4(ANXA13):c.202C>T (p.Leu68Phe)	ANXA13 (L109F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525384	NM_004306.4(ANXA13):c.181G>A (p.Gly61Ser)	ANXA13 (G102S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305087	NM_004306.4(ANXA13):c.128G>T (p.Gly43Val)	ANXA13 (G43V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2320618	NM_004306.4(ANXA13):c.77C>T (p.Ala26Val)	ANXA13 (A67V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2619279	NM_004306.4(ANXA13):c.15+1546A>T	ANXA13 (E40V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2217233	NM_004306.4(ANXA13):c.15+1543G>C	ANXA13 (G39A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2400816	NM_004306.4(ANXA13):c.15+1537G>A	ANXA13 (R37Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2619327	NM_004306.4(ANXA13):c.15+1536C>T	ANXA13 (R37W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2316858	NM_004306.4(ANXA13):c.15+1529C>A	ANXA13 (H34Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2485157	NM_004306.4(ANXA13):c.15+1518C>A	ANXA13 (P31T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2619628	NM_004306.4(ANXA13):c.15+1477A>C	ANXA13 (Q17P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3127268	NM_004306.4(ANXA13):c.15+1476C>A	ANXA13 (Q17K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3299563	NM_004306.4(ANXA13):c.15+1450C>T	ANXA13 (S8L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 32