Colon Cancer: Gene >> CDH2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000269141
Start	28005854:28005854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.842A>G
AA Mutation	p.Lys281Arg(p.K281R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000269141
Start	27990170:27990170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750142878
CDS Mutation	c.1525G>A
AA Mutation	p.Gly509Arg(p.G509R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000269141
Start	27992711:27992711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199882009
CDS Mutation	c.1288C>T
AA Mutation	p.Arg430Trp(p.R430W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000269141
Start	27985554:27985554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1949G>T
AA Mutation	p.Arg650Ile(p.R650I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000269141
Start	27988626:27988626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1639G>T
AA Mutation	p.Asp547Tyr(p.D547Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000269141
Start	28003010:28003010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1007G>T
AA Mutation	p.Gly336Val(p.G336V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000269141
Start	28011945:28011945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.447G>T
AA Mutation	p.Lys149Asn(p.K149N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000269141
Start	27963425:27963425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773655778
CDS Mutation	c.2446G>A
AA Mutation	p.Ala816Thr(p.A816T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000269141
Start	28005912:28005912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.784G>T
AA Mutation	p.Asp262Tyr(p.D262Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000269141
Start	27982989:27982989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2304T>G
AA Mutation	p.Asp768Glu(p.D768E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000269141
Start	27992838:27992838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1161T>G
AA Mutation	p.Phe387Leu(p.F387L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000269141
Start	27985099:27985099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2110G>C
AA Mutation	p.Asp704His(p.D704H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000269141
Start	27990163:27990163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1532A>G
AA Mutation	p.His511Arg(p.H511R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000269141
Start	27963366:27963366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2505C>A
AA Mutation	p.Phe835Leu(p.F835L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000269141
Start	27985203:27985203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2006A>C
AA Mutation	p.Lys669Thr(p.K669T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000269141
Start	27990182:27990182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753588105
CDS Mutation	c.1513C>T
AA Mutation	p.Arg505Cys(p.R505C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000269141
Start	27985609:27985609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1894C>G
AA Mutation	p.Pro632Ala(p.P632A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000269141
Start	27963448:27963448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2423G>A
AA Mutation	p.Arg808Gln(p.R808Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000269141
Start	28003152:28003152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142589795
CDS Mutation	c.865G>A
AA Mutation	p.Val289Ile(p.V289I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000269141
Start	27985056:27985056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140836073
CDS Mutation	c.2153C>T
AA Mutation	p.Ala718Val(p.A718V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000269141
Start	27988562:27988562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1703A>G
AA Mutation	p.Asn568Ser(p.N568S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000269141
Start	27988538:27988538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1727T>G
AA Mutation	p.Leu576Arg(p.L576R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000269141
Start	28013753:28013753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.329A>C
AA Mutation	p.Glu110Ala(p.E110A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000269141
Start	28011846:28011846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.546G>T
AA Mutation	p.Arg182Ser(p.R182S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000269141
Start	27985120:27985120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754165315
CDS Mutation	c.2089C>T
AA Mutation	p.Arg697Cys(p.R697C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000269141
Start	28005895:28005895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.801C>A
AA Mutation	p.Phe267Leu(p.F267L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000269141
Start	28147757:28147757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200711868
CDS Mutation	c.88G>A
AA Mutation	p.Ala30Thr(p.A30T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000269141
Start	28011925:28011925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.467G>T
AA Mutation	p.Arg156Met(p.R156M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000269141
Start	27985198:27985198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2011C>A
AA Mutation	p.Leu671Ile(p.L671I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	missense_variant
Transcription ID	ENST00000269141
Start	28009739:28009739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769462371
CDS Mutation	c.680G>A
AA Mutation	p.Arg227His(p.R227H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000269141
Start	28002999:28002999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1018G>A
AA Mutation	p.Glu340Lys(p.E340K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	missense_variant
Transcription ID	ENST00000269141
Start	27985734:27985734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201191002
CDS Mutation	c.1769C>T
AA Mutation	p.Thr590Met(p.T590M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269141
Start	27985673:27985673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1830A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269141
Start	27985073:27985073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2136G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269141
Start	27952270:27952270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2604G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269141
Start	27993620:27993620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140193518
CDS Mutation	c.1038G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269141
Start	27990186:27990186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1509C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	38
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269141
Start	27993521:27993521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1137T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	39
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269141
Start	27990159:27990159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs190071108
CDS Mutation	c.1536C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	40
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269141
Start	28009738:28009738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201329548
CDS Mutation	c.681C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	41
Mutation Consequence	stop_gained
Transcription ID	ENST00000269141
Start	28147748:28147748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.97A>T
AA Mutation	p.Lys33Ter(p.K33*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CDH2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000269141
Start	27985057:27985057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2152G>A
AA Mutation	p.Ala718Thr(p.A718T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000269141
Start	27952350:27952350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2524G>C
AA Mutation	p.Ala842Pro(p.A842P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000269141
Start	28013754:28013754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs552668002
CDS Mutation	c.328G>C
AA Mutation	p.Glu110Gln(p.E110Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000269141
Start	27952189:27952189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2685G>T
AA Mutation	p.Lys895Asn(p.K895N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000269141
Start	27985717:27985717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1786C>A
AA Mutation	p.Leu596Ile(p.L596I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000269141
Start	27992780:27992780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs568089577
CDS Mutation	c.1219G>A
AA Mutation	p.Asp407Asn(p.D407N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000269141
Start	28013738:28013738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.344G>T
AA Mutation	p.Trp115Leu(p.W115L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000269141
Start	28013866:28013866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.216G>T
AA Mutation	p.Glu72Asp(p.E72D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000269141
Start	27990224:27990224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201148355
CDS Mutation	c.1471G>A
AA Mutation	p.Val491Ile(p.V491I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269141
Start	27990159:27990159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs190071108
CDS Mutation	c.1536C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000269141
Start	28011974:28011974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.418G>T
AA Mutation	p.Glu140Ter(p.E140*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript