"Ambry Genetics"[submitter] AND "NDC80"[gene] - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2325337	NM_006101.3(NDC80):c.29G>T (p.Gly10Val)	NDC80 (G10V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185708	NM_006101.3(NDC80):c.83G>A (p.Gly28Asp)	NDC80 (G28D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268255	NM_006101.3(NDC80):c.164C>T (p.Ser55Leu)	NDC80 (S55L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2331428	NM_006101.3(NDC80):c.289C>G (p.Arg97Gly)	NDC80 (R97G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2307250	NM_006101.3(NDC80):c.364G>C (p.Val122Leu)	NDC80 (V122L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185687	NM_006101.3(NDC80):c.482C>A (p.Pro161His)	NDC80 (P161H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2259336	NM_006101.3(NDC80):c.482C>T (p.Pro161Leu)	NDC80 (P161L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396937	NM_006101.3(NDC80):c.485T>A (p.Phe162Tyr)	NDC80 (F162Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398091	NM_006101.3(NDC80):c.601A>G (p.Ser201Gly)	NDC80 (S201G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185703	NM_006101.3(NDC80):c.625C>A (p.Gln209Lys)	NDC80 (Q209K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185704	NM_006101.3(NDC80):c.778G>A (p.Val260Met)	LOC126862679, NDC80 (V260M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2230930	NM_006101.3(NDC80):c.899A>C (p.Lys300Thr)	LOC126862679, NDC80 (K300T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2269696	NM_006101.3(NDC80):c.929A>G (p.Tyr310Cys)	LOC126862679, NDC80 (Y310C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2538963	NM_006101.3(NDC80):c.940A>G (p.Met314Val)	LOC126862679, NDC80 (M314V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2276742	NM_006101.3(NDC80):c.958C>T (p.His320Tyr)	LOC126862679, NDC80 (H320Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185638	NM_006101.3(NDC80):c.1012G>C (p.Val338Leu)	LOC126862679, NDC80 (V338L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185644	NM_006101.3(NDC80):c.1064T>C (p.Ile355Thr)	NDC80 (I355T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400716	NM_006101.3(NDC80):c.1131G>T (p.Gln377His)	NDC80 (Q377H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185651	NM_006101.3(NDC80):c.1168G>C (p.Glu390Gln)	NDC80 (E390Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2399524	NM_006101.3(NDC80):c.1228A>G (p.Thr410Ala)	NDC80 (T410A)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2205467	NM_006101.3(NDC80):c.1355A>G (p.Lys452Arg)	NDC80 (K452R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2392109	NM_006101.3(NDC80):c.1381C>T (p.Leu461Phe)	NDC80 (L461F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2301621	NM_006101.3(NDC80):c.1552A>C (p.Ile518Leu)	NDC80 (I518L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364908	NM_006101.3(NDC80):c.1684C>T (p.Arg562Trp)	NDC80 (R562W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3185674	NM_006101.3(NDC80):c.1838A>G (p.Glu613Gly)	NDC80 (E613G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 25