Colon Cancer: Gene >> CDH7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000323011
Start	65814509:65814509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763799602
CDS Mutation	c.530C>T
AA Mutation	p.Ala177Val(p.A177V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000323011
Start	65844037:65844037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1207G>T
AA Mutation	p.Asp403Tyr(p.D403Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000323011
Start	65862693:65862693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1640G>T
AA Mutation	p.Arg547Ile(p.R547I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000323011
Start	65880872:65880872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2336G>T
AA Mutation	p.Gly779Val(p.G779V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000323011
Start	65880788:65880788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2252T>A
AA Mutation	p.Ile751Asn(p.I751N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000323011
Start	65880626:65880626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2090C>T
AA Mutation	p.Ala697Val(p.A697V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000323011
Start	65824821:65824821(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	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000323011
Start	65859042:65859042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1490G>T
AA Mutation	p.Gly497Val(p.G497V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000323011
Start	65762981:65762981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.139C>T
AA Mutation	p.Arg47Cys(p.R47C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000323011
Start	65862870:65862870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1817G>A
AA Mutation	p.Ser606Asn(p.S606N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000323011
Start	65862888:65862888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752090043
CDS Mutation	c.1835C>A
AA Mutation	p.Ala612Asp(p.A612D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323011
Start	65862820:65862820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1767C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000323011
Start	65880830:65880830(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2297delG
AA Mutation	p.Gly766AspfsTer34(p.G766Dfs*34)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000323011
Start	65809854:65809854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766062933
CDS Mutation	c.361C>T
AA Mutation	p.Arg121Ter(p.R121*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000323011
Start	65843810:65843810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.982-2A>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CDH7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000323011
Start	65880800:65880800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2264C>A
AA Mutation	p.Ser755Tyr(p.S755Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323011
Start	65809934:65809934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143932384
CDS Mutation	c.441C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000323011
Start	65880601:65880601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2065G>T
AA Mutation	p.Glu689Ter(p.E689*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript