Colon Cancer: Gene >> CDR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370532
Start	140784096:140784096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.271A>G
AA Mutation	p.Met91Val(p.M91V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370532
Start	140783916:140783916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139383933
CDS Mutation	c.451C>T
AA Mutation	p.Arg151Cys(p.R151C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370532
Start	140784114:140784114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.253A>G
AA Mutation	p.Met85Val(p.M85V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370532
Start	140783915:140783915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752950751
CDS Mutation	c.452G>A
AA Mutation	p.Arg151His(p.R151H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370532
Start	140784348:140784348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142598055
CDS Mutation	c.19G>A
AA Mutation	p.Val7Met(p.V7M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000370532
Start	140783862:140783862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.505C>T
AA Mutation	p.Arg169Cys(p.R169C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000370532
Start	140783588:140783588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.779G>T
AA Mutation	p.Trp260Leu(p.W260L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370532
Start	140783637:140783637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.730C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370532
Start	140783741:140783742(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs779058892
CDS Mutation	c.625dupT
AA Mutation	p.Ser209PhefsTer17(p.S209Ffs*17)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CDR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370532
Start	140783692:140783692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.675A>T
AA Mutation	p.Arg225Ser(p.R225S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370532
Start	140783887:140783887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146276960
CDS Mutation	c.480C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370532
Start	140784157:140784157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs191541717
CDS Mutation	c.210G>A
Mutation Classification	Silent
Feature Type	Transcript