Colon Cancer: Gene >> PROC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000234071
Start	127426130:127426130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746989553
CDS Mutation	c.581G>A
AA Mutation	p.Arg194His(p.R194H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000234071
Start	127426181:127426181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199469476
CDS Mutation	c.632G>A
AA Mutation	p.Arg211Gln(p.R211Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000234071
Start	127428461:127428461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.901G>A
AA Mutation	p.Ala301Thr(p.A301T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000234071
Start	127428878:127428878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1318C>T
AA Mutation	p.Arg440Cys(p.R440C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000234071
Start	127428595:127428595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1035C>A
AA Mutation	p.His345Gln(p.H345Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000234071
Start	127427125:127427125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.699G>T
AA Mutation	p.Lys233Asn(p.K233N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000234071
Start	127428517:127428517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.957C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000234071
Start	127428811:127428811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1251G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000234071
Start	127428767:127428767(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1212delG
AA Mutation	p.Met406TrpfsTer15(p.M406Wfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000234071
Start	127422922:127422924(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.245_247delTCT
AA Mutation	p.Phe82del(p.F82del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PROC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000234071
Start	127428860:127428860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766695272
CDS Mutation	c.1300G>A
AA Mutation	p.Val434Ile(p.V434I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript