Related gene-specific medical variations for Gene (Select 84740) - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3274232	NM_001134647.2(AFAP1):c.2177G>A (p.Ser726Asn)	AFAP1, AFAP1-AS1 (S642N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3274196	NM_001134647.2(AFAP1):c.2162C>T (p.Thr721Met)	AFAP1, AFAP1-AS1 (T637M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3091702	NM_001134647.2(AFAP1):c.2396G>A (p.Gly799Glu)	AFAP1, AFAP1-AS1 (G715E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3091697	NM_001134647.2(AFAP1):c.2374C>T (p.Pro792Ser)	AFAP1, AFAP1-AS1 (P708S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3091683	NM_001134647.2(AFAP1):c.2232G>C (p.Lys744Asn)	AFAP1, AFAP1-AS1 (K660N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3091674	NM_001134647.2(AFAP1):c.2132C>T (p.Ala711Val)	AFAP1, AFAP1-AS1 (A627V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3091663	NM_001134647.2(AFAP1):c.2091G>C (p.Glu697Asp)	AFAP1, AFAP1-AS1 (E697D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3091656	NM_001134647.2(AFAP1):c.2039G>A (p.Arg680Gln)	AFAP1, AFAP1-AS1 (R596Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3091650	NM_001134647.2(AFAP1):c.1838C>A (p.Thr613Asn)	AFAP1, AFAP1-AS1 (T529N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2654640	NM_001134647.2(AFAP1):c.2349C>T (p.Ala783=)	AFAP1, AFAP1-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2654639	NM_001134647.2(AFAP1):c.2436C>T (p.Asn812=)	AFAP1, AFAP1-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2622624	NM_001134647.2(AFAP1):c.2432A>G (p.Lys811Arg)	AFAP1, AFAP1-AS1 (K727R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2604165	NM_001134647.2(AFAP1):c.2372C>T (p.Ala791Val)	AFAP1, AFAP1-AS1 (A791V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602924	NM_001134647.2(AFAP1):c.2058C>T (p.Asn686=)	AFAP1, AFAP1-AS1	Single nucleotide variant (synonymous variant +1 more)	not specified +1 more	GLikely benign
Select item 2537687	NM_001134647.2(AFAP1):c.2200G>C (p.Gly734Arg)	AFAP1, AFAP1-AS1 (G650R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2522653	NM_001134647.2(AFAP1):c.2102A>G (p.Gln701Arg)	AFAP1, AFAP1-AS1 (Q617R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2460264	NM_001134647.2(AFAP1):c.2350G>A (p.Val784Ile)	AFAP1, AFAP1-AS1 (V784I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391529	NM_001134647.2(AFAP1):c.2119C>T (p.Arg707Trp)	AFAP1, AFAP1-AS1 (R707W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2369400	NM_001134647.2(AFAP1):c.2389T>A (p.Cys797Ser)	AFAP1, AFAP1-AS1 (C713S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2311373	NM_001134647.2(AFAP1):c.2047A>G (p.Ile683Val)	AFAP1, AFAP1-AS1 (I599V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2292980	NM_001134647.2(AFAP1):c.1871C>T (p.Ala624Val)	AFAP1, AFAP1-AS1 (A540V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2245707	NM_001134647.2(AFAP1):c.2218G>T (p.Ala740Ser)	AFAP1, AFAP1-AS1 (A656S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2240552	NM_001134647.2(AFAP1):c.2093A>G (p.Lys698Arg)	AFAP1, AFAP1-AS1 (K614R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2232666	NM_001134647.2(AFAP1):c.2345C>T (p.Ala782Val)	AFAP1, AFAP1-AS1 (A698V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 730676	NM_001134647.2(AFAP1):c.2115G>A (p.Glu705=)	AFAP1, AFAP1-AS1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign

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Links from Gene

Items: 25