C1708349[trait identifier] AND "Baylor Genetics"[submitter] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 643191	NM_001903.5(CTNNA1):c.2493G>C (p.Gln831His)	CTNNA1 (Q461H +9 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 12587	NM_004985.5(KRAS):c.458A>T (p.Asp153Val)	KRAS (D153V)	Single nucleotide variant (3 prime UTR variant +1 more)	Noonan syndrome	GPathogenic FDA Recognized database
Select item 651982	NM_004360.5(CDH1):c.26C>A (p.Ser9Ter)	CDH1 (S9*)	Single nucleotide variant (nonsense +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GPathogenic FDA Recognized database
Select item 421050	NM_004360.5(CDH1):c.49-3C>A	CDH1	Single nucleotide variant (intron variant)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GUncertain significance FDA Recognized database
Select item 406631	NM_004360.5(CDH1):c.49-2A>G	CDH1	Single nucleotide variant (splice acceptor variant)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GPathogenic FDA Recognized database
Select item 216596	NM_004360.5(CDH1):c.61C>T (p.Leu21Phe)	CDH1 (L21F)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma +2 more	GUncertain significance
Select item 420753	NM_004360.5(CDH1):c.107G>A (p.Ser36Asn)	CDH1 (S36N)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma +3 more	GConflicting classifications of pathogenicity
Select item 489846	NM_004360.5(CDH1):c.112A>C (p.Thr38Pro)	CDH1 (T38P)	Single nucleotide variant (missense variant +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GUncertain significance FDA Recognized database
Select item 187063	NM_004360.5(CDH1):c.112A>G (p.Thr38Ala)	CDH1 (T38A)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma +2 more	GUncertain significance
Select item 231745	NM_004360.5(CDH1):c.125C>T (p.Pro42Leu)	CDH1 (P42L)	Single nucleotide variant (missense variant +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GLikely benign FDA Recognized database
Select item 1778959	NM_004360.5(CDH1):c.172G>T (p.Glu58Ter)	CDH1 (E58*)	Single nucleotide variant (nonsense +1 more)	Familial cancer of breast +2 more	GPathogenic/Likely pathogenic
Select item 406667	NM_004360.5(CDH1):c.199G>A (p.Ala67Thr)	CDH1 (A67T)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 182389	NM_004360.5(CDH1):c.200C>G (p.Ala67Gly)	CDH1 (A67G)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast +4 more	GConflicting classifications of pathogenicity
Select item 820574	NM_004360.5(CDH1):c.203A>G (p.Tyr68Cys)	CDH1 (Y68C)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +4 more	GUncertain significance
Select item 239891	NM_004360.5(CDH1):c.220C>T (p.Arg74Ter)	CDH1 (R74*)	Single nucleotide variant (nonsense +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GPathogenic FDA Recognized database
Select item 419434	NM_004360.5(CDH1):c.244G>A (p.Val82Met)	CDH1 (V82M)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GUncertain significance
Select item 219521	NM_004360.5(CDH1):c.251C>T (p.Thr84Ile)	CDH1 (T84I)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast +3 more	GConflicting classifications of pathogenicity
Select item 239902	NM_004360.5(CDH1):c.261G>C (p.Arg87Ser)	CDH1 (R87S)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma +3 more	GUncertain significance
Select item 187729	NM_004360.5(CDH1):c.304G>T (p.Ala102Ser)	CDH1 (A102S)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast +4 more	GUncertain significance
Select item 532466	NM_004360.5(CDH1):c.313T>A (p.Ser105Thr)	CDH1 (S105T)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 141801	NM_004360.5(CDH1):c.325A>C (p.Lys109Gln)	CDH1 (K109Q)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma +3 more	GUncertain significance
Select item 140878	NM_004360.5(CDH1):c.344C>T (p.Thr115Met)	CDH1 (T115M)	Single nucleotide variant (missense variant +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GLikely benign FDA Recognized database
Select item 486824	NM_004360.5(CDH1):c.382del (p.His128fs)	CDH1 (H128fs)	Deletion (frameshift variant +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GPathogenic FDA Recognized database
Select item 2503034	NM_004360.5(CDH1):c.385C>T (p.Gln129Ter)	CDH1 (Q129*)	Single nucleotide variant (nonsense +1 more)	Familial cancer of breast +1 more	GPathogenic
Select item 141661	NM_004360.5(CDH1):c.387+1G>A	CDH1	Single nucleotide variant (splice donor variant)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GUncertain significance FDA Recognized database
Select item 406644	NM_004360.5(CDH1):c.532-1G>C	CDH1	Single nucleotide variant (splice acceptor variant)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GPathogenic FDA Recognized database
Select item 1749207	NM_004360.5(CDH1):c.570C>G (p.Tyr190Ter)	CDH1 (Y190*)	Single nucleotide variant (nonsense +1 more)	Hereditary cancer-predisposing syndrome +2 more	GPathogenic/Likely pathogenic
Select item 422737	NM_004360.5(CDH1):c.602C>G (p.Pro201Arg)	CDH1 (P201R)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma +4 more	GConflicting classifications of pathogenicity
Select item 629918	NM_004360.5(CDH1):c.620T>C (p.Ile207Thr)	CDH1 (I207T)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 422816	NM_004360.5(CDH1):c.679A>G (p.Thr227Ala)	CDH1 (T227A)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma +3 more	GUncertain significance
Select item 239911	NM_004360.5(CDH1):c.700G>A (p.Ala234Thr)	CDH1 (A234T)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma +2 more	GUncertain significance
Select item 132709	NM_004360.5(CDH1):c.715G>A (p.Gly239Arg)	CDH1 (G239R)	Single nucleotide variant (missense variant +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GPathogenic FDA Recognized database
Select item 420005	NM_004360.5(CDH1):c.731A>G (p.Asp244Gly)	CDH1 (D244G)	Single nucleotide variant (missense variant +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GLikely benign FDA Recognized database
Select item 439473	NM_004360.5(CDH1):c.805G>A (p.Gly269Arg)	CDH1 (G269R)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast +3 more	GUncertain significance
Select item 439045	NM_004360.5(CDH1):c.833-2A>G	CDH1	Single nucleotide variant (splice acceptor variant)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GPathogenic FDA Recognized database
Select item 219957	NM_004360.5(CDH1):c.846G>A (p.Met282Ile)	CDH1 (M282I)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma +4 more	GConflicting classifications of pathogenicity
Select item 141288	NM_004360.5(CDH1):c.854C>T (p.Thr285Ile)	CDH1 (T285I)	Single nucleotide variant (missense variant +1 more)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 532469	NM_004360.5(CDH1):c.865G>A (p.Ala289Thr)	CDH1 (A289T)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 185413	NM_004360.5(CDH1):c.901G>A (p.Ala301Thr)	CDH1 (A301T)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma +3 more	GConflicting classifications of pathogenicity
Select item 823582	NM_004360.5(CDH1):c.995G>T (p.Gly332Val)	CDH1 (G332V)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast +2 more	GUncertain significance
Select item 567658	NM_004360.5(CDH1):c.1003C>G (p.Arg335Gly)	CDH1 (R335G)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast +2 more	GUncertain significance
Select item 183727	NM_004360.5(CDH1):c.1009_1010del (p.Ser337Phefs)	CDH1	Microsatellite (splice acceptor variant)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GPathogenic FDA Recognized database
Select item 1721497	NM_004360.5(CDH1):c.1024A>G (p.Thr342Ala)	CDH1 (T342A)	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary diffuse gastric adenocarcinoma +1 more	GUncertain significance
Select item 2580963	NM_004360.5(CDH1):c.1062del (p.Gly354_Leu355insTer)	CDH1	Deletion (frameshift variant +1 more)	Hereditary diffuse gastric adenocarcinoma +2 more	GConflicting classifications of pathogenicity
Select item 862469	NM_004360.5(CDH1):c.1070C>A (p.Thr357Lys)	CDH1 (T357K)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast +4 more	GUncertain significance
Select item 643357	NM_004360.5(CDH1):c.1079C>G (p.Thr360Arg)	CDH1 (T360R)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast +1 more	GUncertain significance
Select item 406653	NM_004360.5(CDH1):c.1096A>G (p.Thr366Ala)	CDH1 (T366A)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 233204	NM_004360.5(CDH1):c.1097C>G (p.Thr366Ser)	CDH1 (T366S)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast +3 more	GUncertain significance
Select item 1044133	NM_004360.5(CDH1):c.1106A>G (p.Asn369Ser)	CDH1 (N369S)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma +2 more	GUncertain significance
Select item 2441733	NM_004360.5(CDH1):c.1107C>A (p.Asn369Lys)	CDH1 (N369K)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate +2 more	GUncertain significance
Select item 578952	NM_004360.5(CDH1):c.1107del (p.Asn369fs)	CDH1 (N369fs)	Deletion (frameshift variant +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GPathogenic FDA Recognized database
Select item 483234	NM_004360.5(CDH1):c.1112A>G (p.Asn371Ser)	CDH1 (N371S)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 233979	NM_004360.5(CDH1):c.1137+1G>A	CDH1	Single nucleotide variant (splice donor variant)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GPathogenic FDA Recognized database
Select item 1055722	NM_004360.5(CDH1):c.1158G>T (p.Glu386Asp)	CDH1 (E386D)	Single nucleotide variant (5 prime UTR variant +2 more)	Familial cancer of breast +1 more	GUncertain significance
Select item 232232	NM_004360.5(CDH1):c.1183A>G (p.Thr395Ala)	CDH1 (T395A)	Single nucleotide variant (5 prime UTR variant +2 more)	Hereditary diffuse gastric adenocarcinoma +3 more	GConflicting classifications of pathogenicity
Select item 1506353	NM_004360.5(CDH1):c.1192G>A (p.Val398Met)	CDH1 (V398M)	Single nucleotide variant (5 prime UTR variant +2 more)	Hereditary diffuse gastric adenocarcinoma +1 more	GUncertain significance
Select item 422738	NM_004360.5(CDH1):c.1202C>A (p.Ala401Asp)	CDH1 (A401D)	Single nucleotide variant (5 prime UTR variant +2 more)	Hereditary cancer-predisposing syndrome +4 more	GConflicting classifications of pathogenicity
Select item 419071	NM_004360.5(CDH1):c.1202C>T (p.Ala401Val)	CDH1 (A401V)	Single nucleotide variant (5 prime UTR variant +2 more)	Hereditary cancer-predisposing syndrome +4 more	GUncertain significance
Select item 463704	NM_004360.5(CDH1):c.1257TGG[1] (p.Gly421del)	CDH1 (G421del)	Microsatellite (5 prime UTR variant +2 more)	Hereditary diffuse gastric adenocarcinoma +2 more	GUncertain significance
Select item 2035493	NM_004360.5(CDH1):c.1269del (p.Phe423fs)	CDH1 (F423fs)	Deletion (5 prime UTR variant +2 more)	Familial cancer of breast +1 more	GPathogenic/Likely pathogenic
Select item 220738	NM_004360.5(CDH1):c.1303A>G (p.Ile435Val)	CDH1 (I435V)	Single nucleotide variant (5 prime UTR variant +2 more)	Familial cancer of breast +3 more	GUncertain significance
Select item 184950	NM_004360.5(CDH1):c.1315G>A (p.Ala439Thr)	CDH1 (A439T)	Single nucleotide variant (5 prime UTR variant +2 more)	Familial cancer of breast +3 more	GUncertain significance
Select item 127911	NM_004360.5(CDH1):c.1334A>C (p.Glu445Ala)	CDH1 (E445A +1 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 142788	NM_004360.5(CDH1):c.1351A>C (p.Ile451Leu)	CDH1 (I451L +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 182398	NM_004360.5(CDH1):c.1477G>C (p.Val493Leu)	CDH1 (V493L +1 more)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast +4 more	GUncertain significance
Select item 229907	NM_004360.5(CDH1):c.1488_1494del (p.Glu497fs)	CDH1 (E497fs +1 more)	Deletion (frameshift variant +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GPathogenic FDA Recognized database
Select item 1051188	NM_004360.5(CDH1):c.1525A>G (p.Thr509Ala)	CDH1 (T448A +1 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 239884	NM_004360.5(CDH1):c.1526C>A (p.Thr509Asn)	CDH1 (T509N +1 more)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma +3 more	GConflicting classifications of pathogenicity
Select item 187340	NM_004360.5(CDH1):c.1550T>A (p.Met517Lys)	CDH1 (M517K +2 more)	Single nucleotide variant (missense variant +2 more)	Familial cancer of breast +3 more	GUncertain significance
Select item 406624	NM_004360.5(CDH1):c.1565+2dup	CDH1	Duplication (splice donor variant)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GPathogenic FDA Recognized database
Select item 141206	NM_004360.5(CDH1):c.1565+1G>T	CDH1	Single nucleotide variant (splice donor variant)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GPathogenic FDA Recognized database
Select item 127915	NM_004360.5(CDH1):c.1565+1G>A	CDH1	Single nucleotide variant (splice donor variant)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GPathogenic FDA Recognized database
Select item 481704	NM_004360.5(CDH1):c.1566-1G>C	CDH1	Single nucleotide variant (splice acceptor variant +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GUncertain significance FDA Recognized database
Select item 230466	NM_004360.5(CDH1):c.1570C>T (p.Arg524Trp)	CDH1 (R524W +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GUncertain significance
Select item 449339	NM_004360.5(CDH1):c.1590dup (p.Asn531fs)	CDH1 (N15fs +2 more)	Duplication (frameshift variant +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GPathogenic FDA Recognized database
Select item 479491	NM_004360.5(CDH1):c.1612G>T (p.Asp538Tyr)	CDH1 (D538Y +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma +3 more	GUncertain significance
Select item 234554	NM_004360.5(CDH1):c.1679C>G (p.Thr560Arg)	CDH1 (T560R +2 more)	Single nucleotide variant (missense variant +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GPathogenic FDA Recognized database
Select item 188085	NM_004360.5(CDH1):c.1679C>T (p.Thr560Met)	CDH1 (T560M +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma +4 more	GUncertain significance
Select item 849571	NM_004360.5(CDH1):c.1693A>G (p.Ile565Val)	CDH1 (I49V +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 279746	NM_004360.5(CDH1):c.1700C>T (p.Ala567Val)	CDH1 (A567V +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma +2 more	GUncertain significance
Select item 234181	NM_004360.5(CDH1):c.1707C>A (p.Asp569Glu)	CDH1 (D569E +2 more)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast +3 more	GUncertain significance
Select item 428630	NM_004360.5(CDH1):c.1711+5G>A	CDH1	Single nucleotide variant (intron variant)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GUncertain significance FDA Recognized database
Select item 532437	NM_004360.5(CDH1):c.1772A>G (p.Asn591Ser)	CDH1 (N591S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified +3 more	GUncertain significance
Select item 186627	NM_004360.5(CDH1):c.1789C>A (p.Pro597Thr)	CDH1 (P597T +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma +3 more	GUncertain significance
Select item 12241	NM_004360.5(CDH1):c.1792C>T (p.Arg598Ter)	CDH1 (R598* +2 more)	Single nucleotide variant (nonsense +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GPathogenic FDA Recognized database
Select item 188221	NM_004360.5(CDH1):c.1793G>A (p.Arg598Gln)	CDH1 (R598Q +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma +4 more	GConflicting classifications of pathogenicity
Select item 231651	NM_004360.5(CDH1):c.1832T>A (p.Val611Asp)	CDH1 (V611D +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma +2 more	GUncertain significance
Select item 1444594	NM_004360.5(CDH1):c.1864A>T (p.Asn622Tyr)	CDH1 (N561Y +2 more)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast +2 more	GUncertain significance
Select item 928253	NM_004360.5(CDH1):c.1868C>T (p.Thr623Ile)	CDH1 (T562I +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GUncertain significance
Select item 847107	NM_004360.5(CDH1):c.1914G>A (p.Trp638Ter)	CDH1 (W122* +2 more)	Single nucleotide variant (nonsense +1 more)	Hereditary diffuse gastric adenocarcinoma +1 more	GPathogenic/Likely pathogenic
Select item 463737	NM_004360.5(CDH1):c.1946C>T (p.Ser649Phe)	CDH1 (S649F +2 more)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma +3 more	GUncertain significance
Select item 1374871	NM_004360.5(CDH1):c.1960C>A (p.Pro654Thr)	CDH1 (P593T +2 more)	Single nucleotide variant (missense variant +1 more)	Familial cancer of breast +3 more	GUncertain significance
Select item 182376	NM_004360.5(CDH1):c.1979dup (p.Gly661_Asp662insTer)	CDH1	Duplication (frameshift variant)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GPathogenic FDA Recognized database
Select item 481684	NM_004360.5(CDH1):c.1979T>A (p.Val660Glu)	CDH1 (V660E +3 more)	Single nucleotide variant (missense variant)	Hereditary diffuse gastric adenocarcinoma +2 more	GUncertain significance
Select item 185252	NM_004360.5(CDH1):c.1999del (p.Leu667fs)	CDH1 (L667fs +3 more)	Deletion (frameshift variant)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GPathogenic FDA Recognized database
Select item 141376	NM_004360.5(CDH1):c.2017C>A (p.Gln673Lys)	CDH1 (Q673K +3 more)	Single nucleotide variant (missense variant)	Breast and/or ovarian cancer +4 more	GConflicting classifications of pathogenicity
Select item 182402	NM_004360.5(CDH1):c.2026G>A (p.Asp676Asn)	CDH1 (D676N +3 more)	Single nucleotide variant (missense variant)	Familial cancer of breast +3 more	GConflicting classifications of pathogenicity
Select item 140781	NM_004360.5(CDH1):c.2064_2065del (p.Cys688_Glu689delinsTer)	CDH1	Microsatellite (nonsense)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GPathogenic FDA Recognized database
Select item 532459	NM_004360.5(CDH1):c.2165-1G>C	CDH1	Single nucleotide variant (splice acceptor variant)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GLikely pathogenic FDA Recognized database
Select item 239890	NM_004360.5(CDH1):c.2165T>C (p.Ile722Thr)	CDH1 (I722T +3 more)	Single nucleotide variant (missense variant)	Hereditary diffuse gastric adenocarcinoma +2 more	GUncertain significance

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