Colon Cancer: Gene >> CYP2D6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360608
Start	42128941:42128941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.509G>A
AA Mutation	p.Arg170His(p.R170H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360608
Start	42127458:42127458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146271511
CDS Mutation	c.1162C>T
AA Mutation	p.Arg388Cys(p.R388C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360608
Start	42129827:42129827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267608276
CDS Mutation	c.263G>A
AA Mutation	p.Arg88His(p.R88H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360608
Start	42126863:42126863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1303C>T
AA Mutation	p.Pro435Ser(p.P435S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360608
Start	42129173:42129173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377591409
CDS Mutation	c.365C>T
AA Mutation	p.Ala122Val(p.A122V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000360608
Start	42126988:42126988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757030056
CDS Mutation	c.1178C>T
AA Mutation	p.Thr393Met(p.T393M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000360608
Start	42127575:42127575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774382844
CDS Mutation	c.1045G>A
AA Mutation	p.Asp349Asn(p.D349N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000360608
Start	42127473:42127473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs75386357
CDS Mutation	c.1147G>A
AA Mutation	p.Glu383Lys(p.E383K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000360608
Start	42127527:42127527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769351604
CDS Mutation	c.1093C>T
AA Mutation	p.Arg365Cys(p.R365C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360608
Start	42126619:42126619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs28371736
CDS Mutation	c.1449C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360608
Start	42128347:42128347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.670C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360608
Start	42127506:42127506(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1114delC
AA Mutation	p.Leu372TrpfsTer3(p.L372Wfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CYP2D6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360608
Start	42128320:42128320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.697A>T
AA Mutation	p.Ile233Phe(p.I233F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360608
Start	42129160:42129160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369043970
CDS Mutation	c.378C>T
Mutation Classification	Silent
Feature Type	Transcript