Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CDH18

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000274170
Start	19571784:19571784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1048G>A
AA Mutation	p.Ala350Thr(p.A350T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000274170
Start	19591061:19591061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.995A>G
AA Mutation	p.Lys332Arg(p.K332R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000274170
Start	19543980:19543980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1279G>T
AA Mutation	p.Asp427Tyr(p.D427Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000274170
Start	19483331:19483331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1852G>A
AA Mutation	p.Ala618Thr(p.A618T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000274170
Start	19473482:19473482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2117C>A
AA Mutation	p.Thr706Asn(p.T706N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000274170
Start	19483406:19483406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1777A>G
AA Mutation	p.Arg593Gly(p.R593G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000274170
Start	19747019:19747019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.446T>A
AA Mutation	p.Val149Glu(p.V149E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000274170
Start	19721411:19721411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.579C>A
AA Mutation	p.Asn193Lys(p.N193K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000274170
Start	19520689:19520689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1480A>G
AA Mutation	p.Ile494Val(p.I494V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000274170
Start	19591085:19591085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.971C>A
AA Mutation	p.Thr324Asn(p.T324N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000274170
Start	19483519:19483519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1664G>A
AA Mutation	p.Arg555Lys(p.R555K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000274170
Start	19838807:19838807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.180C>A
AA Mutation	p.Phe60Leu(p.F60L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000274170
Start	19473639:19473639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1960A>T
AA Mutation	p.Asn654Tyr(p.N654Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000274170
Start	19571763:19571763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759919566
CDS Mutation	c.1069C>T
AA Mutation	p.Arg357Cys(p.R357C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000274170
Start	19838883:19838883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.104G>T
AA Mutation	p.Arg35Ile(p.R35I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000274170
Start	19543946:19543946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1313G>C
AA Mutation	p.Gly438Ala(p.G438A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000274170
Start	19473429:19473429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2170G>C
AA Mutation	p.Asp724His(p.D724H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000274170
Start	19571762:19571762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148450624
CDS Mutation	c.1070G>A
AA Mutation	p.Arg357His(p.R357H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000274170
Start	19747031:19747031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.434T>G
AA Mutation	p.Phe145Cys(p.F145C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000274170
Start	19473569:19473569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2030G>T
AA Mutation	p.Arg677Met(p.R677M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000274170
Start	19483505:19483505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1678G>A
AA Mutation	p.Val560Ile(p.V560I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000274170
Start	19483391:19483391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755435892
CDS Mutation	c.1792C>T
AA Mutation	p.Arg598Trp(p.R598W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274170
Start	19747072:19747072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.393T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274170
Start	19473610:19473610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367628466
CDS Mutation	c.1989C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274170
Start	19473481:19473481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2118C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274170
Start	19591084:19591084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.972C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274170
Start	19721363:19721363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267600591
CDS Mutation	c.627C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274170
Start	19520669:19520669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1500T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274170
Start	19483383:19483383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1800C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274170
Start	19473418:19473418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2181T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274170
Start	19571692:19571692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1140A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274170
Start	19520663:19520663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1506T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000274170
Start	19543967:19543967(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1292delT
AA Mutation	p.Phe431SerfsTer39(p.F431Sfs*39)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000274170
Start	19483482:19483482(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1701delC
AA Mutation	p.Ile568LeufsTer2(p.I568Lfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000274170
Start	19838950:19838950(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.37delC
AA Mutation	p.Leu13Ter(p.L13*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	stop_gained
Transcription ID	ENST00000274170
Start	19483511:19483511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1672C>T
AA Mutation	p.Arg558Ter(p.R558*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	37
Mutation Consequence	stop_gained
Transcription ID	ENST00000274170
Start	19473297:19473297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2302G>T
AA Mutation	p.Gly768Ter(p.G768*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	38
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000274170
Start	19483435:19483436(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1745_1747dupGCA
AA Mutation	p.Ser582dup(p.S582dup)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CDH18

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000274170
Start	19483417:19483417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1766G>T
AA Mutation	p.Cys589Phe(p.C589F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000274170
Start	19473680:19473680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1919A>G
AA Mutation	p.Lys640Arg(p.K640R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000274170
Start	19571763:19571763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759919566
CDS Mutation	c.1069C>T
AA Mutation	p.Arg357Cys(p.R357C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000274170
Start	19591060:19591060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.996G>T
AA Mutation	p.Lys332Asn(p.K332N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000274170
Start	19473584:19473584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2015A>T
AA Mutation	p.Asp672Val(p.D672V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274170
Start	19571716:19571716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1116C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274170
Start	19483473:19483473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1710C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000274170
Start	19473252:19473252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764848176
CDS Mutation	c.2347G>T
AA Mutation	p.Glu783Ter(p.E783*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript