"Color Diagnostics, LLC DBA Color Health"[submitter] AND "CDH1"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 127904	NM_004360.5(CDH1):c.-18C>T	LOC130059290, CDH1	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 928191	NM_004360.5(CDH1):c.-17G>C	CDH1, LOC130059290	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 629093	NM_004360.5(CDH1):c.-15C>G	CDH1, LOC130059290	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 920396	NM_004360.5(CDH1):c.-10C>G	CDH1, LOC130059290	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 633149	NM_004360.5(CDH1):c.-8G>A	CDH1	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 517866	NM_004360.5(CDH1):c.-8G>C	CDH1	Single nucleotide variant (5 prime UTR variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 628145	NM_004360.5(CDH1):c.-2C>T	CDH1	Single nucleotide variant (5 prime UTR variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 532474	NM_004360.5(CDH1):c.2T>G (p.Met1Arg)	CDH1 (M1R)	Single nucleotide variant (missense variant +2 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GPathogenic FDA Recognized database
Select item 183998	NM_004360.5(CDH1):c.4G>A (p.Gly2Ser)	CDH1 (G2S)	Single nucleotide variant (missense variant +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GLikely benign FDA Recognized database
Select item 631262	NM_004360.5(CDH1):c.5G>A (p.Gly2Asp)	CDH1 (G2D)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 239909	NM_004360.5(CDH1):c.5G>T (p.Gly2Val)	CDH1 (G2V)	Single nucleotide variant (missense variant +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GUncertain significance FDA Recognized database
Select item 629094	NM_004360.5(CDH1):c.7C>A (p.Pro3Thr)	CDH1 (P3T)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 142469	NM_004360.5(CDH1):c.8C>G (p.Pro3Arg)	CDH1 (P3R)	Single nucleotide variant (missense variant +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GLikely benign FDA Recognized database
Select item 918853	NM_004360.5(CDH1):c.11G>A (p.Trp4Ter)	CDH1 (W4*)	Single nucleotide variant (nonsense +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GPathogenic FDA Recognized database
Select item 548782	NM_004360.5(CDH1):c.12G>A (p.Trp4Ter)	CDH1 (W4*)	Single nucleotide variant (nonsense +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GPathogenic FDA Recognized database
Select item 184111	NM_004360.5(CDH1):c.15C>T (p.Ser5=)	CDH1	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GLikely benign
Select item 923416	NM_004360.5(CDH1):c.20_21delinsAT (p.Ser7Asn)	CDH1 (S7N)	Indel (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 820715	NM_004360.5(CDH1):c.20G>C (p.Ser7Thr)	CDH1 (S7T)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1171841	NM_004360.5(CDH1):c.21C>A (p.Ser7Arg)	CDH1 (S7R)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 2775020	NM_004360.5(CDH1):c.24C>A (p.Leu8=)	CDH1	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 630530	NM_004360.5(CDH1):c.24C>G (p.Leu8=)	CDH1	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GLikely benign
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 184065	NM_004360.5(CDH1):c.27G>A (p.Ser9=)	CDH1	Single nucleotide variant (synonymous variant +1 more)	not specified +4 more	GConflicting classifications of pathogenicity
Select item 918393	NM_004360.5(CDH1):c.28G>C (p.Ala10Pro)	CDH1 (A10P)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 220798	NM_004360.5(CDH1):c.32TGC[6] (p.Leu15dup)	CDH1	Microsatellite (inframe_insertion +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GLikely benign FDA Recognized database
Select item 142455	NM_004360.5(CDH1):c.32TGC[7] (p.Leu14_Leu15dup)	CDH1	Microsatellite (inframe_insertion +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GLikely benign FDA Recognized database
Select item 628358	NM_004360.5(CDH1):c.32TGC[2] (p.Leu13_Leu15del)	CDH1	Microsatellite (inframe_deletion +1 more)	Hereditary diffuse gastric adenocarcinoma +1 more	GUncertain significance
Select item 491533	NM_004360.5(CDH1):c.30G>T (p.Ala10=)	CDH1	Single nucleotide variant (synonymous variant +1 more)	Hereditary diffuse gastric adenocarcinoma +2 more	GLikely benign
Select item 182377	NM_004360.5(CDH1):c.33G>C (p.Leu11=)	CDH1	Single nucleotide variant (synonymous variant +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GLikely benign FDA Recognized database
Select item 414047	NM_004360.5(CDH1):c.34C>T (p.Leu12=)	CDH1	Single nucleotide variant (synonymous variant +1 more)	Hereditary diffuse gastric adenocarcinoma +1 more	GLikely benign
Select item 2775021	NM_004360.5(CDH1):c.39G>T (p.Leu13=)	CDH1	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 919859	NM_004360.5(CDH1):c.45G>A (p.Leu15=)	CDH1	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +3 more	GLikely benign
Select item 628144	NM_004360.5(CDH1):c.47A>T (p.Gln16Leu)	CDH1 (Q16L)	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 491543	NM_004360.5(CDH1):c.48+5C>T	CDH1	Single nucleotide variant (intron variant)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GLikely benign FDA Recognized database
Select item 491542	NM_004360.5(CDH1):c.48+5_48+6delinsGT	CDH1	Indel (intron variant)	Hereditary diffuse gastric adenocarcinoma +1 more	GConflicting classifications of pathogenicity
Select item 491541	NM_004360.5(CDH1):c.48+5_48+6delinsAT	CDH1	Indel (intron variant)	Hereditary diffuse gastric adenocarcinoma +1 more	GConflicting classifications of pathogenicity
Select item 491540	NM_004360.5(CDH1):c.48+5_48+6delinsTT	CDH1	Indel (intron variant)	Hereditary diffuse gastric adenocarcinoma +1 more	GConflicting classifications of pathogenicity
Select item 140784	NM_004360.5(CDH1):c.48+5C>G	CDH1	Single nucleotide variant (intron variant)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GBenign FDA Recognized database
Select item 1171549	NM_004360.5(CDH1):c.48+6_48+8delinsTCA	CDH1	Indel (intron variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 922365	NM_004360.5(CDH1):c.48+6_48+7delinsTG	CDH1	Indel (intron variant)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 136692	NM_004360.5(CDH1):c.48+6C>T	CDH1	Single nucleotide variant (intron variant)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GBenign FDA Recognized database
Select item 136068	NM_004360.3(CDH1):c.48+6_48+7delinsTT	CDH1	Indel (intron variant)	Hereditary cancer-predisposing syndrome +2 more	GLikely benign
Select item 918387	NM_004360.5(CDH1):c.48+12C>G	CDH1	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 491539	NM_004360.5(CDH1):c.48+12C>A	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma +1 more	GLikely benign
Select item 182378	NM_004360.5(CDH1):c.48+15_48+16del	CDH1	Deletion (intron variant)	Familial cancer of breast +6 more	GBenign/Likely benign
Select item 391234	NM_004360.5(CDH1):c.49-20C>T	CDH1	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +2 more	GLikely benign
Select item 491545	NM_004360.5(CDH1):c.49-19T>C	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma +1 more	GConflicting classifications of pathogenicity
Select item 491544	NM_004360.5(CDH1):c.49-16C>T	CDH1	Single nucleotide variant (intron variant)	not specified +2 more	GLikely benign
Select item 372019	NM_004360.5(CDH1):c.49-16C>G	CDH1	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 491546	NM_004360.5(CDH1):c.49-8dup	CDH1	Duplication (intron variant)	Hereditary cancer-predisposing syndrome +2 more	GBenign/Likely benign
Select item 386324	NM_004360.5(CDH1):c.49-11C>G	CDH1	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 629936	NM_004360.5(CDH1):c.49-10C>T	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma +1 more	GLikely benign
Select item 516511	NM_004360.5(CDH1):c.49-9C>A	CDH1	Single nucleotide variant (intron variant)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GLikely benign FDA Recognized database
Select item 387465	NM_004360.5(CDH1):c.49-8C>T	CDH1	Single nucleotide variant (intron variant)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GLikely benign FDA Recognized database
Select item 386415	NM_004360.5(CDH1):c.49-8C>A	CDH1	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome +2 more	GConflicting classifications of pathogenicity
Select item 630992	NM_004360.5(CDH1):c.49-6C>A	CDH1	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 925068	NM_004360.5(CDH1):c.49-5C>T	CDH1	Single nucleotide variant (intron variant)	Hereditary diffuse gastric adenocarcinoma +1 more	GConflicting classifications of pathogenicity
Select item 380961	NM_004360.5(CDH1):c.49-4C>A	CDH1	Single nucleotide variant (intron variant)	not specified +1 more	GConflicting classifications of pathogenicity
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 142294	NM_004360.5(CDH1):c.49-3C>T	CDH1	Single nucleotide variant (intron variant)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GLikely benign FDA Recognized database
Select item 479528	NM_004360.5(CDH1):c.56C>G (p.Ser19Cys)	CDH1 (S19C)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma +2 more	GUncertain significance
Select item 230175	NM_004360.5(CDH1):c.61C>G (p.Leu21Val)	CDH1 (L21V)	Single nucleotide variant (missense variant +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GUncertain significance 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 421115	NM_004360.5(CDH1):c.62T>C (p.Leu21Pro)	CDH1 (L21P)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided +2 more	GUncertain significance
Select item 479510	NM_004360.5(CDH1):c.65G>A (p.Cys22Tyr)	CDH1 (C22Y)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GUncertain significance
Select item 1332253	NM_004360.5(CDH1):c.66C>G (p.Cys22Trp)	CDH1 (C22W)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma +1 more	GUncertain significance
Select item 232158	NM_004360.5(CDH1):c.66C>T (p.Cys22=)	CDH1	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 186050	NM_004360.5(CDH1):c.69G>A (p.Gln23=)	CDH1	Single nucleotide variant (synonymous variant +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GLikely benign FDA Recognized database
Select item 1332198	NM_004360.5(CDH1):c.72G>A (p.Glu24=)	CDH1	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 230669	NM_004360.5(CDH1):c.76G>C (p.Glu26Gln)	CDH1 (E26Q)	Single nucleotide variant (missense variant +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GUncertain significance FDA Recognized database
Select item 239913	NM_004360.5(CDH1):c.79C>T (p.Pro27Ser)	CDH1 (P27S)	Single nucleotide variant (missense variant +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GUncertain significance FDA Recognized database
Select item 926222	NM_004360.5(CDH1):c.81C>T (p.Pro27=)	CDH1	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 136070	NM_004360.5(CDH1):c.84C>T (p.Cys28=)	CDH1	Single nucleotide variant (synonymous variant +1 more)	Hereditary diffuse gastric adenocarcinoma +8 more	GBenign/Likely benign
Select item 532480	NM_004360.5(CDH1):c.86A>G (p.His29Arg)	CDH1 (H29R)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma +1 more	GUncertain significance
Select item 1331759	NM_004360.5(CDH1):c.87C>A (p.His29Gln)	CDH1 (H29Q)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma +1 more	GUncertain significance
Select item 127933	NM_004360.5(CDH1):c.88C>A (p.Pro30Thr)	CDH1 (P30T)	Single nucleotide variant (missense variant +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GBenign FDA Recognized database
Select item 233438	NM_004360.5(CDH1):c.89C>G (p.Pro30Arg)	CDH1 (P30R)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma +1 more	GUncertain significance
Select item 479505	NM_004360.5(CDH1):c.90T>C (p.Pro30=)	CDH1	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GLikely benign
Select item 823156	NM_004360.5(CDH1):c.92G>A (p.Gly31Asp)	CDH1 (G31D)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma +1 more	GUncertain significance
Select item 479502	NM_004360.5(CDH1):c.93C>T (p.Gly31=)	CDH1	Single nucleotide variant (synonymous variant +1 more)	Hereditary diffuse gastric adenocarcinoma +2 more	GConflicting classifications of pathogenicity
Select item 923087	NM_004360.5(CDH1):c.100G>A (p.Ala34Thr)	CDH1 (A34T)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 925227	NM_004360.5(CDH1):c.102C>G (p.Ala34=)	CDH1	Single nucleotide variant (synonymous variant +1 more)	Hereditary diffuse gastric adenocarcinoma +1 more	GLikely benign
Select item 219699	NM_004360.5(CDH1):c.102C>T (p.Ala34=)	CDH1	Single nucleotide variant (synonymous variant +1 more)	Hereditary diffuse gastric adenocarcinoma +1 more	GLikely benign
Select item 2775022	NM_004360.5(CDH1):c.104A>C (p.Glu35Ala)	CDH1 (E35A)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 420753	NM_004360.5(CDH1):c.107G>A (p.Ser36Asn)	CDH1 (S36N)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 232808	NM_004360.5(CDH1):c.111C>T (p.Tyr37=)	CDH1	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
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 231383	NM_004360.5(CDH1):c.113C>A (p.Thr38Lys)	CDH1 (T38K)	Single nucleotide variant (missense variant +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GLikely benign FDA Recognized database
Select item 133850	NM_004360.5(CDH1):c.113C>T (p.Thr38Met)	CDH1 (T38M)	Single nucleotide variant (missense variant +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GLikely benign FDA Recognized database
Select item 184799	NM_004360.5(CDH1):c.114G>A (p.Thr38=)	CDH1	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign
Select item 184482	NM_004360.5(CDH1):c.114G>C (p.Thr38=)	CDH1	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +2 more	GBenign/Likely benign
Select item 941101	NM_004360.5(CDH1):c.119C>T (p.Thr40Met)	CDH1 (T40M)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma +1 more	GUncertain significance
Select item 184377	NM_004360.5(CDH1):c.120G>A (p.Thr40=)	CDH1	Single nucleotide variant (synonymous variant +1 more)	CDH1-related diffuse gastric and lobular breast cancer syndrome	GLikely benign FDA Recognized database
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 925885	NM_004360.5(CDH1):c.128G>T (p.Arg43Leu)	CDH1 (R43L)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 481703	NM_004360.5(CDH1):c.131G>T (p.Arg44Leu)	CDH1 (R44L)	Single nucleotide variant (missense variant +1 more)	Hereditary diffuse gastric adenocarcinoma +1 more	GUncertain significance
Select item 2775023	NM_004360.5(CDH1):c.135C>A (p.His45Gln)	CDH1 (H45Q)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 491495	NM_004360.5(CDH1):c.136C>T (p.Leu46=)	CDH1	Single nucleotide variant (5 prime UTR variant +1 more)	Hereditary diffuse gastric adenocarcinoma +1 more	GLikely benign
Select item 628376	NM_004360.5(CDH1):c.138G>A (p.Leu46=)	CDH1	Single nucleotide variant (synonymous variant +1 more)	Hereditary cancer-predisposing syndrome +1 more	GLikely benign

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