Colon Cancer: Gene >> CDH6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265071
Start	31297313:31297313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.548C>T
AA Mutation	p.Ala183Val(p.A183V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265071
Start	31305204:31305204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1030A>G
AA Mutation	p.Thr344Ala(p.T344A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265071
Start	31317735:31317735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1693C>A
AA Mutation	p.Leu565Ile(p.L565I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265071
Start	31297295:31297295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.530T>G
AA Mutation	p.Phe177Cys(p.F177C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265071
Start	31322854:31322854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777622672
CDS Mutation	c.1919G>A
AA Mutation	p.Arg640Gln(p.R640Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265071
Start	31267653:31267653(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	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265071
Start	31313392:31313392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752932258
CDS Mutation	c.1328C>T
AA Mutation	p.Ser443Leu(p.S443L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265071
Start	31323004:31323004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2069G>T
AA Mutation	p.Arg690Met(p.R690M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000265071
Start	31294196:31294196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.463A>G
AA Mutation	p.Asn155Asp(p.N155D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000265071
Start	31323018:31323018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2083G>A
AA Mutation	p.Glu695Lys(p.E695K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000265071
Start	31322958:31322958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2023G>A
AA Mutation	p.Gly675Ser(p.G675S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000265071
Start	31297316:31297316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764565018
CDS Mutation	c.551C>T
AA Mutation	p.Thr184Met(p.T184M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000265071
Start	31317846:31317846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1804G>A
AA Mutation	p.Ala602Thr(p.A602T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000265071
Start	31322832:31322832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1897T>C
AA Mutation	p.Phe633Leu(p.F633L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000265071
Start	31317679:31317679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1637C>T
AA Mutation	p.Thr546Met(p.T546M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000265071
Start	31297389:31297389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.624T>G
AA Mutation	p.Phe208Leu(p.F208L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265071
Start	31322957:31322957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763884564
CDS Mutation	c.2022C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265071
Start	31316233:31316233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1416A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265071
Start	31322915:31322915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1980C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265071
Start	31323176:31323176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2241G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265071
Start	31323017:31323017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764269155
CDS Mutation	c.2082C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265071
Start	31322855:31322855(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1926delA
AA Mutation	p.Glu643SerfsTer3(p.E643Sfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000265071
Start	31313409:31313409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1345G>T
AA Mutation	p.Glu449Ter(p.E449*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000265071
Start	31313423:31313423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1359G>A
AA Mutation	p.Trp453Ter(p.W453*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000265071
Start	31323000:31323000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771395680
CDS Mutation	c.2065C>T
AA Mutation	p.Arg689Ter(p.R689*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CDH6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265071
Start	31322854:31322854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777622672
CDS Mutation	c.1919G>A
AA Mutation	p.Arg640Gln(p.R640Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265071
Start	31313400:31313400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1336C>A
AA Mutation	p.Leu446Ile(p.L446I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265071
Start	31313380:31313380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771406443
CDS Mutation	c.1316C>T
AA Mutation	p.Ser439Leu(p.S439L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265071
Start	31317439:31317439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1577C>A
AA Mutation	p.Ser526Tyr(p.S526Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265071
Start	31299606:31299606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753390985
CDS Mutation	c.786C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265071
Start	31322853:31322854(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1919dupG
AA Mutation	p.Glu643ArgfsTer13(p.E643Rfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript