Colon Cancer: Gene >> CDHR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000623527
Start	84208243:84208243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1033G>A
AA Mutation	p.Asp345Asn(p.D345N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000623527
Start	84212243:84212243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1618G>A
AA Mutation	p.Ala540Thr(p.A540T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000623527
Start	84195527:84195527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757172364
CDS Mutation	c.89A>G
AA Mutation	p.Asn30Ser(p.N30S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000623527
Start	84203067:84203067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.727G>T
AA Mutation	p.Ala243Ser(p.A243S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000623527
Start	84202981:84202981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.641A>G
AA Mutation	p.Asp214Gly(p.D214G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000623527
Start	84208772:84208772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752039450
CDS Mutation	c.1211G>A
AA Mutation	p.Gly404Asp(p.G404D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000623527
Start	84203067:84203067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.727G>A
AA Mutation	p.Ala243Thr(p.A243T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000623527
Start	84213160:84213160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1852A>G
AA Mutation	p.Asn618Asp(p.N618D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000623527
Start	84214457:84214457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2416G>A
AA Mutation	p.Ala806Thr(p.A806T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000623527
Start	84196543:84196543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.190G>A
AA Mutation	p.Gly64Arg(p.G64R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000623527
Start	84214282:84214282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2241G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CDHR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000623527
Start	84204551:84204551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773335171
CDS Mutation	c.808G>A
AA Mutation	p.Ala270Thr(p.A270T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript