Colon Cancer: Gene >> FST

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000256759
Start	53485957:53485957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371840444
CDS Mutation	c.959C>T
AA Mutation	p.Ser320Leu(p.S320L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000256759
Start	53484070:53484070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.498G>T
AA Mutation	p.Lys166Asn(p.K166N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000256759
Start	53484267:53484267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.695G>A
AA Mutation	p.Gly232Glu(p.G232E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256759
Start	53480833:53480833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.42G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000256759
Start	53485035:53485035(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.765delA
AA Mutation	p.Lys255AsnfsTer43(p.K255Nfs*43)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000256759
Start	53484210:53484211(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.638_639insA
AA Mutation	p.Tyr214LeufsTer23(p.Y214Lfs*23)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000256759
Start	53484211:53484212(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.639_640insATGAATAGG
AA Mutation	p.Thr213_Tyr214insMetAsnArg(p.T213_Y214insMNR)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FST

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000256759
Start	53483672:53483672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.446G>T
AA Mutation	p.Arg149Ile(p.R149I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000256759
Start	53480843:53480843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150238035
CDS Mutation	c.52C>T
AA Mutation	p.Leu18Phe(p.L18F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000256759
Start	53486028:53486028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1030T>G
AA Mutation	p.Trp344Gly(p.W344G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript