HOMER3[gene] and "single gene"[properties] - ClinVar

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Items: 30

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2465157	NM_004838.4(HOMER3):c.1081C>A (p.Pro361Thr)	HOMER3 (P358T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2289393	NM_004838.4(HOMER3):c.1003G>A (p.Ala335Thr)	HOMER3 (A299T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2223140	NM_004838.4(HOMER3):c.1001G>A (p.Arg334Gln)	HOMER3 (R331Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3106479	NM_004838.4(HOMER3):c.999C>T (p.Gly333=)	HOMER3	Single nucleotide variant (synonymous variant +1 more)	not specified	GLikely benign
Select item 2347110	NM_004838.4(HOMER3):c.985C>T (p.Arg329Trp)	HOMER3 (R326W +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2409980	NM_004838.4(HOMER3):c.979C>T (p.Arg327Trp)	HOMER3 (R324W +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2543919	NM_004838.4(HOMER3):c.955G>C (p.Glu319Gln)	HOMER3 (E283Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3106477	NM_004838.4(HOMER3):c.914C>T (p.Ala305Val)	HOMER3 (A305V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2370697	NM_004838.4(HOMER3):c.869G>A (p.Arg290His)	HOMER3 (R254H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2216743	NM_004838.4(HOMER3):c.844C>T (p.Arg282Cys)	HOMER3 (R282C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3106476	NM_004838.4(HOMER3):c.824A>G (p.Lys275Arg)	HOMER3 (K275R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 710762	NM_004838.4(HOMER3):c.777G>A (p.Gln259=)	HOMER3	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 781464	NM_004838.4(HOMER3):c.738T>C (p.Gly246=)	HOMER3	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 3106475	NM_004838.4(HOMER3):c.683G>A (p.Arg228Gln)	HOMER3 (R192Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2346074	NM_004838.4(HOMER3):c.677G>A (p.Arg226Gln)	HOMER3 (R226Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2358799	NM_004838.4(HOMER3):c.661C>T (p.Arg221Cys)	HOMER3 (R185C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3106474	NM_004838.4(HOMER3):c.626C>G (p.Ala209Gly)	HOMER3 (A173G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2356382	NM_004838.4(HOMER3):c.548T>A (p.Val183Glu)	HOMER3 (V147E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2408928	NM_004838.4(HOMER3):c.449G>A (p.Gly150Asp)	HOMER3 (G114D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2445979	NM_004838.4(HOMER3):c.434G>A (p.Ser145Asn)	HOMER3 (S145N +1 more)	Single nucleotide variant (missense variant +1 more)	Keratoconus	GLikely pathogenic
Select item 2365254	NM_004838.4(HOMER3):c.415C>T (p.Pro139Ser)	HOMER3 (P139S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 780553	NM_004838.4(HOMER3):c.412-4C>A	HOMER3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3106473	NM_004838.4(HOMER3):c.400G>A (p.Ala134Thr)	HOMER3 (A134T)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GLikely benign
Select item 3106472	NM_004838.4(HOMER3):c.370G>A (p.Gly124Arg)	HOMER3 (G124R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2348750	NM_004838.4(HOMER3):c.351G>T (p.Arg117Ser)	HOMER3 (R117S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2537963	NM_004838.4(HOMER3):c.281C>T (p.Ala94Val)	HOMER3 (A94V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3106471	NM_004838.4(HOMER3):c.260C>T (p.Thr87Ile)	HOMER3 (T87I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2536148	NM_004838.4(HOMER3):c.124G>T (p.Asp42Tyr)	HOMER3 (D42Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2340377	NM_004838.4(HOMER3):c.103C>G (p.Leu35Val)	HOMER3 (L35V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2601390	NM_004838.4(HOMER3):c.37C>T (p.Arg13Trp)	HOMER3 (R13W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 30