Colon Cancer: Gene >> MYLIP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356840
Start	16145162:16145162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1093G>A
AA Mutation	p.Gly365Ser(p.G365S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356840
Start	16130629:16130629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.160T>G
AA Mutation	p.Leu54Val(p.L54V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356840
Start	16145253:16145253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1184T>A
AA Mutation	p.Ile395Asn(p.I395N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356840
Start	16145071:16145071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs72833427
CDS Mutation	c.1002C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356840
Start	16145242:16145242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs1060901
CDS Mutation	c.1173C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356840
Start	16143855:16143855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.819A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356840
Start	16145302:16145302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148878853
CDS Mutation	c.1233C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356840
Start	16145014:16145015(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.949dupA
AA Mutation	p.Arg317LysfsTer8(p.R317Kfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356840
Start	16143150:16143151(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.595_596insGAATT
AA Mutation	p.Lys199ArgfsTer26(p.K199Rfs*26)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MYLIP

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000356840
Start	16143075:16143075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.520C>T
AA Mutation	p.Gln174Ter(p.Q174*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript