Colon Cancer: Gene >> VANGL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310260
Start	115664012:115664012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765459331
CDS Mutation	c.556C>T
AA Mutation	p.Arg186Cys(p.R186C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310260
Start	115691336:115691336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1532C>T
AA Mutation	p.Ser511Phe(p.S511F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000310260
Start	115684006:115684006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1009G>A
AA Mutation	p.Asp337Asn(p.D337N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000310260
Start	115685450:115685450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755820435
CDS Mutation	c.1237C>T
AA Mutation	p.Arg413Trp(p.R413W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310260
Start	115659683:115659683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201840785
CDS Mutation	c.114C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310260
Start	115651458:115651458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.45T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310260
Start	115685392:115685392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370067272
CDS Mutation	c.1179C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000310260
Start	115663965:115663965(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.515delT
AA Mutation	p.Phe172SerfsTer99(p.F172Sfs*99)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000310260
Start	115664061:115664061(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.610delT
AA Mutation	p.Tyr204ThrfsTer67(p.Y204Tfs*67)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000310260
Start	115691153:115691153(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1351delC
AA Mutation	p.Leu451CysfsTer21(p.L451Cfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000310260
Start	115664060:115664061(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.610dupT
AA Mutation	p.Tyr204LeufsTer88(p.Y204Lfs*88)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> VANGL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310260
Start	115684004:115684004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1007G>T
AA Mutation	p.Arg336Met(p.R336M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript