ClinVar (all) for Orgtrack (Select 509096) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2503041	NM_004360.5(CDH1):c.519A>C (p.Lys173Asn)	CDH1 (K173N)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2503040	NM_004360.5(CDH1):c.497dup (p.Asn166fs)	CDH1 (N166fs)	Duplication (frameshift variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GPathogenic
Select item 2503039	NM_004360.5(CDH1):c.479_480del (p.Pro160fs)	CDH1 (P160fs)	Deletion (frameshift variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GPathogenic
Select item 2503038	NM_004360.5(CDH1):c.437C>T (p.Ser146Phe)	CDH1 (S146F)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2503037	NM_004360.5(CDH1):c.416del (p.Leu139fs)	CDH1 (L139fs)	Deletion (frameshift variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GPathogenic
Select item 2503036	NM_004360.4:c.(387+1_388-1)_(1711+1_1712-1)dup	CDH1	Duplication	Hereditary diffuse gastric adenocarcinoma	GPathogenic
Select item 2503035	NM_004360.5(CDH1):c.387+76C>A	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2503034	NM_004360.5(CDH1):c.385C>T (p.Gln129Ter)	CDH1 (Q129*)	Single nucleotide variant (nonsense +1 more)	Hereditary diffuse gastric adenocarcinoma +1 more	GPathogenic
Select item 2503033	NC_000016.10:g.(?_68737292)_(68835537_?)del	LOC128772407, CDH1 +24 more	Deletion	Hereditary diffuse gastric adenocarcinoma	GPathogenic
Select item 2503032	NM_004360.5(CDH1):c.336del (p.Val114fs)	CDH1 (V114fs)	Deletion (frameshift variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GPathogenic
Select item 2503031	NM_004360.5(CDH1):c.326del (p.Lys109fs)	CDH1 (K109fs)	Deletion (frameshift variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GPathogenic
Select item 2503030	NC_000016.10:g.(?_68737292)_(68738411_?)del	CDH1, LOC130059290	Deletion	Hereditary diffuse gastric adenocarcinoma	GPathogenic
Select item 2503029	NM_004360.5(CDH1):c.281_283delinsGT (p.Pro94fs)	CDH1 (P94fs)	Indel (frameshift variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GPathogenic
Select item 2503028	NM_004360.5(CDH1):c.271T>C (p.Phe91Leu)	CDH1 (F91L)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2503027	NC_000016.10:g.(?_68737292)_(68737463_?)del	CDH1, LOC130059290	Deletion	Hereditary diffuse gastric adenocarcinoma	GLikely pathogenic
Select item 2503026	NM_004360.4:c.(163+1_164-1)_(1137+1_1138-1)del	CDH1	Deletion	Hereditary diffuse gastric adenocarcinoma	GPathogenic
Select item 2503025	NM_004360.4:c.(163+1_164-1)_(387+1_388-1)del	CDH1	Deletion	Hereditary diffuse gastric adenocarcinoma	GPathogenic
Select item 2503024	NM_004360.5(CDH1):c.164-6579_164-1957del	CDH1	Deletion (intron variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2503023	NM_004360.5(CDH1):c.163+29142_164-30404del	CDH1, LOC128772407 +1 more	Deletion (intron variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2503022	NM_004360.5(CDH1):c.163+115A>T	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2503021	NM_004360.5(CDH1):c.163+90T>G	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2503020	NM_004360.5(CDH1):c.163+81G>A	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2503019	NM_004360.5(CDH1):c.163+75A>T	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2503018	NM_004360.5(CDH1):c.163+14G>A	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2503017	NM_004360.5(CDH1):c.129_163+9dup	CDH1	Duplication (splice donor variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2503016	NM_004360.5(CDH1):c.*55G>A	CDH1	Single nucleotide variant (3 prime UTR variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2503015	NM_004360.5(CDH1):c.*29C>A	CDH1	Single nucleotide variant (3 prime UTR variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2503014	NM_004360.5(CDH1):c.*7C>G	CDH1	Single nucleotide variant (3 prime UTR variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2503013	NM_004360.5(CDH1):c.2520del (p.Glu841fs)	CDH1 (E186fs +3 more)	Deletion (frameshift variant)	Hereditary diffuse gastric adenocarcinoma	GLikely pathogenic
Select item 2503012	NM_004360.5(CDH1):c.87C>G (p.His29Gln)	CDH1 (H29Q)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2503011	NC_000016.10:g.(?_68833290)_(68835537_?)del	CDH1	Deletion	Hereditary diffuse gastric adenocarcinoma	GLikely pathogenic
Select item 2503010	NM_004360.5(CDH1):c.2440-52A>G	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2503009	NM_004360.5(CDH1):c.2440-118G>A	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2503008	NM_004360.5(CDH1):c.86dup (p.His29fs)	CDH1 (H29fs)	Duplication (frameshift variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GPathogenic
Select item 2503007	NM_004360.5(CDH1):c.2440-396_*223del	CDH1	Deletion (splice acceptor variant)	Hereditary diffuse gastric adenocarcinoma	GLikely pathogenic
Select item 2503006	NM_004360.5(CDH1):c.2439+53G>A	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2503005	NM_004360.5(CDH1):c.2439+45C>G	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2503004	NM_004360.5(CDH1):c.2439+10C>A	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2503003	NM_004360.5(CDH1):c.2439+3A>G	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2503002	NM_004360.5(CDH1):c.83G>A (p.Cys28Tyr)	CDH1 (C28Y)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma +1 more	GUncertain significance
Select item 2503001	NM_004360.5(CDH1):c.2315T>A (p.Leu772Gln)	CDH1 (L117Q +3 more)	Single nucleotide variant (missense variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2503000	NM_004360.5(CDH1):c.2296-41T>C	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2502999	NM_004360.5(CDH1):c.2296-42C>G	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2502998	NM_004360.5(CDH1):c.2296-60C>A	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2502997	NM_004360.5(CDH1):c.2295+46G>A	CDH1	Single nucleotide variant (intron variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2502996	NM_004360.5(CDH1):c.2295+45C>T	CDH1	Single nucleotide variant (intron variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2502995	NM_004360.5(CDH1):c.2266G>T (p.Asp756Tyr)	CDH1 (D101Y +3 more)	Single nucleotide variant (missense variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2502994	NM_004360.5(CDH1):c.2220del (p.Leu741fs)	CDH1 (L225fs +3 more)	Deletion (frameshift variant)	Hereditary diffuse gastric adenocarcinoma	GPathogenic
Select item 2502993	NM_004360.5(CDH1):c.2165-59C>T	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2502992	NM_004360.5(CDH1):c.2165-111G>C	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2502991	NM_004360.5(CDH1):c.2164+2T>A	CDH1	Single nucleotide variant (splice donor variant)	Hereditary diffuse gastric adenocarcinoma	GPathogenic
Select item 2502990	NM_004360.5(CDH1):c.2116C>T (p.Gln706Ter)	CDH1 (Q190* +3 more)	Single nucleotide variant (nonsense)	Hereditary diffuse gastric adenocarcinoma	GPathogenic
Select item 2502989	NM_004360.5(CDH1):c.2114del (p.Leu705fs)	CDH1 (L189fs +3 more)	Deletion (frameshift variant)	Hereditary diffuse gastric adenocarcinoma	GPathogenic
Select item 2502988	NM_004360.5(CDH1):c.2062del (p.Cys688fs)	CDH1 (C172fs +3 more)	Deletion (frameshift variant)	Hereditary diffuse gastric adenocarcinoma	GLikely pathogenic
Select item 2502987	NM_004360.5(CDH1):c.2031del (p.Gln677_Val678insTer)	CDH1	Deletion (frameshift variant)	Hereditary diffuse gastric adenocarcinoma	GPathogenic
Select item 2502986	NM_004360.5(CDH1):c.1965del (p.Met656fs)	CDH1 (M140fs +2 more)	Deletion (frameshift variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GPathogenic
Select item 2502985	NM_004360.5(CDH1):c.1937-29T>C	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma +1 more	GConflicting classifications of pathogenicity
Select item 2502984	NM_004360.5(CDH1):c.1937-37C>G	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2502983	NM_004360.5(CDH1):c.1937-111C>A	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2502982	NM_004360.5(CDH1):c.1906_1907insA (p.Ala636fs)	CDH1 (A120fs +2 more)	Insertion (frameshift variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GPathogenic
Select item 2502981	NM_004360.5(CDH1):c.55_74del (p.Ser19fs)	CDH1 (S19fs)	Deletion (frameshift variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GPathogenic
Select item 2502980	NM_004360.5(CDH1):c.1795del (p.Thr599fs)	CDH1 (T538fs +2 more)	Deletion (frameshift variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GPathogenic/Likely pathogenic
Select item 2502979	NM_004360.5(CDH1):c.1786G>T (p.Glu596Ter)	CDH1 (E535* +2 more)	Single nucleotide variant (nonsense +1 more)	Hereditary diffuse gastric adenocarcinoma	GPathogenic
Select item 2502978	NM_004360.5(CDH1):c.1748T>G (p.Leu583Arg)	CDH1 (L522R +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2502977	NM_004360.5(CDH1):c.53C>A (p.Ser18Tyr)	CDH1 (S18Y)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2502976	NM_004360.5(CDH1):c.1712-54dup	CDH1	Duplication (intron variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2502975	NM_004360.5(CDH1):c.1712-103A>G	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2502974	NM_004360.5(CDH1):c.1712-127G>A	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2502973	NM_004360.5(CDH1):c.1712-128C>T	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2502972	NM_004360.5(CDH1):c.1712-151G>T	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2502971	NM_004360.5(CDH1):c.1712-161G>A	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2502970	NM_004360.5(CDH1):c.1712-168G>C	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2502969	NM_004360.5(CDH1):c.1712-184A>G	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2502968	NM_004360.5(CDH1):c.1651G>T (p.Glu551Ter)	CDH1 (E35* +2 more)	Single nucleotide variant (nonsense +1 more)	Hereditary cancer-predisposing syndrome +1 more	GPathogenic
Select item 2502967	NM_004360.5(CDH1):c.1624A>G (p.Ile542Val)	CDH1 (I26V +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2502966	NM_004360.4:c.(1565+1_1566-1)_(2164+1_2165-1)del	CDH1	Deletion	Hereditary diffuse gastric adenocarcinoma	GPathogenic
Select item 2502965	NM_004360.4:c.(1565+1_1566-1)_(1711+1_1712-1)del	CDH1	Deletion	Hereditary diffuse gastric adenocarcinoma	GPathogenic
Select item 2502964	NM_004360.5(CDH1):c.1566-38T>G	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2502963	NM_004360.5(CDH1):c.48+83C>T	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2502962	NM_004360.5(CDH1):c.1519T>A (p.Ser507Thr)	CDH1 (S446T +1 more)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2502961	NM_004360.5(CDH1):c.48+63T>C	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2502960	NM_004360.5(CDH1):c.1466dup (p.Pro489_Glu490insTer)	CDH1	Duplication (frameshift variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GPathogenic
Select item 2502959	NM_004360.5(CDH1):c.48+52C>A	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2502958	NM_004360.5(CDH1):c.1416dup (p.Val473fs)	CDH1 (V412fs +1 more)	Duplication (frameshift variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GPathogenic
Select item 2502957	NM_004360.5(CDH1):c.1404del (p.Ser469fs)	CDH1 (S408fs +1 more)	Deletion (frameshift variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GPathogenic
Select item 2502956	NM_004360.5(CDH1):c.1401del (p.Thr468fs)	CDH1 (T407fs +1 more)	Deletion (frameshift variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GPathogenic
Select item 2502955	NM_004360.5(CDH1):c.48+41C>T	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2502954	NM_004360.5(CDH1):c.1321-36C>T	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GBenign
Select item 2502953	NM_004360.5(CDH1):c.1321-37T>C	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2502952	NM_004360.5(CDH1):c.1321-49A>G	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2502951	NM_004360.5(CDH1):c.1321-65A>T	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2502950	NM_004360.5(CDH1):c.1321-140T>C	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2502949	NM_004360.5(CDH1):c.1320+43C>G	CDH1	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2502948	NM_004360.5(CDH1):c.1320+35C>T	CDH1	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary diffuse gastric adenocarcinoma	GBenign
Select item 2502947	NM_004360.4:c.(1320+1_1321-1)_(1711+1_1712-1)del	CDH1	Deletion	Hereditary diffuse gastric adenocarcinoma	GPathogenic
Select item 2502946	NM_004360.5(CDH1):c.1320+1G>A	CDH1	Single nucleotide variant (5 prime UTR variant +2 more)	Hereditary diffuse gastric adenocarcinoma	GConflicting classifications of pathogenicity
Select item 2502945	NM_004360.5(CDH1):c.1264C>T (p.Gln422Ter)	CDH1 (Q422*)	Single nucleotide variant (5 prime UTR variant +2 more)	Hereditary diffuse gastric adenocarcinoma	GPathogenic
Select item 2502944	NM_004360.5(CDH1):c.1222G>T (p.Ala408Ser)	CDH1 (A408S)	Single nucleotide variant (5 prime UTR variant +2 more)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance
Select item 2502943	NM_004360.5(CDH1):c.1141A>T (p.Lys381Ter)	CDH1 (K381*)	Single nucleotide variant (5 prime UTR variant +2 more)	Hereditary diffuse gastric adenocarcinoma	GPathogenic
Select item 2502942	NM_004360.5(CDH1):c.1138-22G>T	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma	GUncertain significance

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