Colon Cancer: Gene >> DLD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000205402
Start	107902345:107902345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.219T>G
AA Mutation	p.Asn73Lys(p.N73K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000205402
Start	107904959:107904959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.339G>A
AA Mutation	p.Met113Ile(p.M113I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000205402
Start	107917394:107917394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1168C>T
AA Mutation	p.Pro390Ser(p.P390S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000205402
Start	107916862:107916862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371807385
CDS Mutation	c.944G>A
AA Mutation	p.Arg315Gln(p.R315Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000205402
Start	107915550:107915550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.729A>C
AA Mutation	p.Glu243Asp(p.E243D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000205402
Start	107915551:107915551(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.734delT
AA Mutation	p.Leu245Ter(p.L245*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000205402
Start	107906311:107906311(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.633delA
AA Mutation	p.Val212PhefsTer12(p.V212Ffs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000205402
Start	107906310:107906311(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.633dupA
AA Mutation	p.Val212SerfsTer32(p.V212Sfs*32)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> DLD

No Mutation Annotation!