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

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Items: 31

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2531398	NM_001386991.1(BANP):c.61G>A (p.Asp21Asn)	BANP (D21N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2340162	NM_001386991.1(BANP):c.106G>A (p.Glu36Lys)	BANP (E36K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2237680	NM_001386991.1(BANP):c.228A>T (p.Gln76His)	BANP (Q68H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2370715	NM_001386991.1(BANP):c.278C>T (p.Thr93Met)	BANP (T85M +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2357415	NM_001386991.1(BANP):c.293G>A (p.Ser98Asn)	BANP (S98N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3132970	NM_001386991.1(BANP):c.340C>G (p.Gln114Glu)	BANP (Q106E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2339711	NM_001386991.1(BANP):c.444C>G (p.Asn148Lys)	BANP (N148K +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2458813	NM_001386991.1(BANP):c.494G>A (p.Arg165His)	BANP (R132H +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549654	NM_001386991.1(BANP):c.497G>A (p.Arg166Gln)	BANP (R127Q +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3132971	NM_001386991.1(BANP):c.509T>C (p.Ile170Thr)	BANP (I137T +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260349	NM_001386991.1(BANP):c.607A>G (p.Ser203Gly)	BANP (S100G +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2646966	NM_001386991.1(BANP):c.618C>T (p.Ile206=)	BANP	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 487782	NM_001386991.1(BANP):c.692A>G (p.Asn231Ser)	BANP (N192S +6 more)	Single nucleotide variant (missense variant)	Ependymoma	GUncertain significance
Select item 756317	NM_001386991.1(BANP):c.975G>A (p.Thr325=)	BANP	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2338187	NM_001386991.1(BANP):c.1010C>T (p.Ala337Val)	BANP (A234V +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2226535	NM_001386991.1(BANP):c.1058C>T (p.Pro353Leu)	BANP (P211L +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2609986	NM_001386991.1(BANP):c.1076G>T (p.Ser359Ile)	BANP (S320I +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3132963	NM_001386991.1(BANP):c.1103C>T (p.Pro368Leu)	BANP (P226L +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3132964	NM_001386991.1(BANP):c.1115C>A (p.Pro372Gln)	BANP (P378Q +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260350	NM_001386991.1(BANP):c.1126G>T (p.Ala376Ser)	BANP (A273S +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546807	NM_001386991.1(BANP):c.1129C>G (p.Leu377Val)	BANP (L377V +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2387736	NM_001386991.1(BANP):c.1144G>T (p.Ala382Ser)	BANP (A279S +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3132966	NM_001386991.1(BANP):c.1259C>T (p.Thr420Met)	BANP (T275M +12 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2250577	NM_001386991.1(BANP):c.1306G>A (p.Gly436Ser)	BANP (G400S +12 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3132967	NM_001386991.1(BANP):c.1427C>T (p.Ala476Val)	BANP (A351V +16 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2288256	NM_001386991.1(BANP):c.1462G>A (p.Asp488Asn)	BANP (D360N +16 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2250908	NM_001386991.1(BANP):c.1508C>T (p.Thr503Met)	BANP (T339M +16 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2481538	NM_001386991.1(BANP):c.1520A>G (p.Gln507Arg)	BANP (Q482R +16 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260348	NM_001386991.1(BANP):c.1544C>T (p.Thr515Met)	BANP (T348M +16 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555322	NM_001386991.1(BANP):c.1564C>T (p.Leu522Phe)	BANP (L355F +16 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3132968	NM_001386991.1(BANP):c.1584G>C (p.Gln528His)	BANP (Q364H +16 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 31