ASAP1[gene] and "single gene"[properties] - ClinVar

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Items: 33

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3130034	NM_018482.4(ASAP1):c.3371T>C (p.Val1124Ala)	ASAP1 (V1124A +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611267	NM_018482.4(ASAP1):c.3325A>G (p.Ile1109Val)	ASAP1 (I1102V +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2558423	NM_018482.4(ASAP1):c.3191C>T (p.Thr1064Met)	ASAP1 (T1007M +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2658816	NM_018482.4(ASAP1):c.3162G>A (p.Thr1054=)	ASAP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2369753	NM_018482.4(ASAP1):c.3136G>A (p.Asp1046Asn)	ASAP1 (D989N +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2314445	NM_018482.4(ASAP1):c.3104C>G (p.Ala1035Gly)	ASAP1 (A1028G +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130033	NM_018482.4(ASAP1):c.3068C>T (p.Pro1023Leu)	ASAP1 (P966L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130032	NM_018482.4(ASAP1):c.2867C>T (p.Pro956Leu)	ASAP1 (P949L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2658817	NM_018482.4(ASAP1):c.2814C>T (p.Asp938=)	ASAP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2474249	NM_018482.4(ASAP1):c.2619T>G (p.Phe873Leu)	ASAP1 (F819L +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3316951	NM_018482.4(ASAP1):c.2497G>A (p.Gly833Arg)	ASAP1 (G826R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2533321	NM_018482.4(ASAP1):c.2452G>A (p.Gly818Ser)	ASAP1 (G818S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2622483	NM_018482.4(ASAP1):c.2431C>A (p.Leu811Ile)	ASAP1 (L804I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3130031	NM_018482.4(ASAP1):c.2429C>T (p.Pro810Leu)	ASAP1 (P803L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3130030	NM_018482.4(ASAP1):c.2363C>T (p.Thr788Met)	ASAP1 (T791M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371781	NM_018482.4(ASAP1):c.2362A>G (p.Thr788Ala)	ASAP1 (T788A +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2509458	NM_018482.4(ASAP1):c.2249A>G (p.Lys750Arg)	ASAP1 (K750R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2600650	NM_018482.4(ASAP1):c.2237C>T (p.Ser746Phe)	ASAP1 (S746F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130029	NM_018482.4(ASAP1):c.2048C>G (p.Thr683Ser)	ASAP1 (T683S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402395	NM_018482.4(ASAP1):c.1858G>A (p.Val620Ile)	ASAP1 (V620I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344556	NM_018482.4(ASAP1):c.1825G>A (p.Val609Ile)	ASAP1 (V602I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468529	NM_018482.4(ASAP1):c.1748A>G (p.Tyr583Cys)	ASAP1 (Y576C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2545001	NM_018482.4(ASAP1):c.1741C>A (p.Gln581Lys)	ASAP1 (Q574K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2614801	NM_018482.4(ASAP1):c.1649A>G (p.His550Arg)	ASAP1 (H543R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2557753	NM_018482.4(ASAP1):c.1298G>A (p.Ser433Asn)	ASAP1 (S433N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130028	NM_018482.4(ASAP1):c.1295A>G (p.Asn432Ser)	ASAP1 (N432S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 769344	NM_018482.4(ASAP1):c.1169-8dup	ASAP1	Duplication (intron variant)	not provided	GBenign
Select item 2240957	NM_018482.4(ASAP1):c.1055G>A (p.Gly352Glu)	ASAP1 (G345E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 769345	NM_018482.4(ASAP1):c.789G>A (p.Gln263=)	ASAP1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3316962	NM_018482.4(ASAP1):c.722T>C (p.Ile241Thr)	ASAP1 (I241T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2600593	NM_018482.4(ASAP1):c.635G>A (p.Arg212His)	ASAP1 (R212H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2481470	NM_018482.4(ASAP1):c.626A>G (p.Lys209Arg)	ASAP1 (K209R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2620881	NM_018482.4(ASAP1):c.400A>T (p.Asn134Tyr)	ASAP1 (N134Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 33