Colon Cancer: Gene >> MYC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377970
Start	127738699:127738699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.437C>T
AA Mutation	p.Ser146Leu(p.S146L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377970
Start	127738687:127738687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.425C>T
AA Mutation	p.Ala142Val(p.A142V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377970
Start	127738589:127738589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.327C>A
AA Mutation	p.Asp109Glu(p.D109E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377970
Start	127738525:127738525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.263G>A
AA Mutation	p.Gly88Asp(p.G88D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377970
Start	127740900:127740900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761932135
CDS Mutation	c.1262G>A
AA Mutation	p.Arg421Gln(p.R421Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000377970
Start	127738438:127738438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.176C>T
AA Mutation	p.Pro59Leu(p.P59L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377970
Start	127740538:127740538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.900C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377970
Start	127740859:127740859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1221A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377970
Start	127740832:127740833(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1194_1195insT
AA Mutation	p.Ala399CysfsTer18(p.A399Cfs*18)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MYC

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377970
Start	127740739:127740739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746692226
CDS Mutation	c.1101G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000377970
Start	127740483:127740485(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.847_849delTCT
AA Mutation	p.Ser283del(p.S283del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript