CDH6[gene] and "single gene"[properties] - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3265325	NM_004932.4(CDH6):c.119T>C (p.Leu40Pro)	CDH6 (L40P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517773	NM_004932.4(CDH6):c.167T>A (p.Met56Lys)	CDH6 (M56K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248875	NM_004932.4(CDH6):c.248G>A (p.Arg83Lys)	CDH6 (R83K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2388214	NM_004932.4(CDH6):c.367G>A (p.Val123Ile)	CDH6 (V123I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141316	NM_004932.4(CDH6):c.389C>T (p.Ala130Val)	CDH6 (A130V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2394662	NM_004932.4(CDH6):c.415G>A (p.Val139Met)	CDH6 (V139M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3265324	NM_004932.4(CDH6):c.760G>A (p.Val254Met)	CDH6 (V254M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141317	NM_004932.4(CDH6):c.985A>G (p.Ile329Val)	CDH6 (I329V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2275622	NM_004932.4(CDH6):c.1070G>A (p.Arg357Gln)	CDH6 (R357Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2291160	NM_004932.4(CDH6):c.1224A>C (p.Gln408His)	CDH6 (Q408H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495349	NM_004932.4(CDH6):c.1330A>C (p.Lys444Gln)	CDH6 (K444Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225663	NM_004932.4(CDH6):c.1406G>A (p.Ser469Asn)	CDH6 (S469N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528460	NM_004932.4(CDH6):c.1549C>T (p.Pro517Ser)	CDH6 (P517S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141313	NM_004932.4(CDH6):c.1760G>A (p.Arg587Gln)	CDH6 (R587Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141314	NM_004932.4(CDH6):c.1838C>G (p.Thr613Arg)	CDH6 (T613R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489955	NM_004932.4(CDH6):c.1901C>G (p.Ala634Gly)	CDH6 (A634G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542054	NM_004932.4(CDH6):c.2042A>G (p.Glu681Gly)	CDH6 (E681G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511621	NM_004932.4(CDH6):c.2056A>G (p.Asn686Asp)	CDH6 (N686D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2323200	NM_004932.4(CDH6):c.2216C>T (p.Ala739Val)	CDH6 (A739V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141315	NM_004932.4(CDH6):c.2236G>T (p.Val746Leu)	CDH6 (V746L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2624259	NM_004932.4(CDH6):c.2243A>G (p.Asp748Gly)	CDH6 (D748G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530479	NM_004932.4(CDH6):c.2306A>G (p.Asp769Gly)	CDH6 (D769G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463125	NM_004932.4(CDH6):c.2324A>G (p.Lys775Arg)	CDH6 (K775R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3265323	NM_004932.4(CDH6):c.2339T>C (p.Met780Thr)	CDH6 (M780T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 563054	GRCh37/hg19 5p13.3(chr5:31002679-31214471)x3	CDH6	Copy number gain	not provided	GUncertain significance

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Items: 25