"Ambry Genetics"[submitter] AND "CDH7"[gene] - ClinVar

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Items: 46

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2494011	NM_004361.5(CDH7):c.278C>G (p.Ser93Cys)	CDH7 (S93C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463644	NM_004361.5(CDH7):c.397G>A (p.Val133Met)	CDH7 (V133M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2591743	NM_004361.5(CDH7):c.475A>G (p.Thr159Ala)	CDH7 (T159A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3265328	NM_004361.5(CDH7):c.651C>G (p.Asn217Lys)	CDH7 (N217K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478120	NM_004361.5(CDH7):c.685G>A (p.Val229Ile)	CDH7 (V229I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2591639	NM_004361.5(CDH7):c.800A>G (p.Tyr267Cys)	CDH7 (Y267C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588860	NM_004361.5(CDH7):c.806A>G (p.Tyr269Cys)	CDH7 (Y269C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348726	NM_004361.5(CDH7):c.839T>C (p.Val280Ala)	CDH7 (V280A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2295436	NM_004361.5(CDH7):c.887A>T (p.Glu296Val)	CDH7 (E296V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3265329	NM_004361.5(CDH7):c.901A>G (p.Ile301Val)	CDH7 (I301V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141332	NM_004361.5(CDH7):c.932A>G (p.Lys311Arg)	CDH7 (K311R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2466638	NM_004361.5(CDH7):c.953C>A (p.Thr318Asn)	CDH7 (T318N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141318	NM_004361.5(CDH7):c.1013C>T (p.Thr338Met)	CDH7 (T338M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369342	NM_004361.5(CDH7):c.1082C>T (p.Thr361Met)	CDH7 (T361M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516964	NM_004361.5(CDH7):c.1084A>G (p.Thr362Ala)	CDH7 (T362A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2520790	NM_004361.5(CDH7):c.1100T>C (p.Ile367Thr)	CDH7 (I367T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141320	NM_004361.5(CDH7):c.1108G>A (p.Asp370Asn)	CDH7 (D370N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141321	NM_004361.5(CDH7):c.1147C>G (p.Pro383Ala)	CDH7 (P383A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141322	NM_004361.5(CDH7):c.1161G>A (p.Ser387=)	CDH7	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3141323	NM_004361.5(CDH7):c.1217C>A (p.Ser406Tyr)	CDH7 (S406Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3265327	NM_004361.5(CDH7):c.1487C>A (p.Pro496Gln)	CDH7 (P496Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3265331	NM_004361.5(CDH7):c.1534T>C (p.Ser512Pro)	CDH7 (S512P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2260519	NM_004361.5(CDH7):c.1606A>T (p.Asn536Tyr)	CDH7 (N536Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491374	NM_004361.5(CDH7):c.1631T>G (p.Leu544Arg)	CDH7 (L544R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515425	NM_004361.5(CDH7):c.1640G>C (p.Arg547Thr)	CDH7 (R547T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602275	NM_004361.5(CDH7):c.1645G>A (p.Gly549Ser)	CDH7 (G549S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2614913	NM_004361.5(CDH7):c.1651C>T (p.Arg551Trp)	CDH7 (R551W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141324	NM_004361.5(CDH7):c.1684A>G (p.Ile562Val)	CDH7 (I562V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141325	NM_004361.5(CDH7):c.1694T>G (p.Val565Gly)	CDH7 (V565G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141326	NM_004361.5(CDH7):c.1706C>A (p.Ser569Tyr)	CDH7 (S569Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2509060	NM_004361.5(CDH7):c.1732C>G (p.Leu578Val)	CDH7 (L578V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2476355	NM_004361.5(CDH7):c.1852T>G (p.Leu618Val)	CDH7 (L618V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3265326	NM_004361.5(CDH7):c.1873C>T (p.Leu625Phe)	CDH7, LOC126862782 (L625F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215720	NM_004361.5(CDH7):c.1886C>G (p.Thr629Ser)	CDH7, LOC126862782 (T629S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2473873	NM_004361.5(CDH7):c.1900A>G (p.Lys634Glu)	CDH7, LOC126862782 (K634E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2262500	NM_004361.5(CDH7):c.1904A>G (p.Lys635Arg)	CDH7, LOC126862782 (K635R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3265330	NM_004361.5(CDH7):c.1909C>A (p.Pro637Thr)	CDH7, LOC126862782 (P637T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141327	NM_004361.5(CDH7):c.1918T>C (p.Phe640Leu)	CDH7, LOC126862782 (F640L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409607	NM_004361.5(CDH7):c.1923C>A (p.Asp641Glu)	CDH7, LOC126862782 (D641E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3265332	NM_004361.5(CDH7):c.1937T>A (p.Ile646Asn)	CDH7, LOC126862782 (I646N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350185	NM_004361.5(CDH7):c.2002A>G (p.Met668Val)	CDH7, LOC126862782 (M668V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271835	NM_004361.5(CDH7):c.2015G>A (p.Arg672Lys)	CDH7, LOC126862782 (R672K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141329	NM_004361.5(CDH7):c.2026G>A (p.Val676Ile)	CDH7, LOC126862782 (V676I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141330	NM_004361.5(CDH7):c.2114T>C (p.Val705Ala)	CDH7, LOC126862782 (V705A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347837	NM_004361.5(CDH7):c.2256C>G (p.Ser752Arg)	CDH7, LOC126862782 (S752R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141331	NM_004361.5(CDH7):c.2320G>A (p.Asp774Asn)	CDH7, LOC126862782 (D774N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 46