Colon Cancer: Gene >> RAG2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311485
Start	36593837:36593837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.332C>A
AA Mutation	p.Ser111Tyr(p.S111Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311485
Start	36593561:36593561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.608G>A
AA Mutation	p.Gly203Glu(p.G203E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311485
Start	36593942:36593942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.227C>T
AA Mutation	p.Ala76Val(p.A76V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000311485
Start	36593393:36593393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.776C>A
AA Mutation	p.Ser259Tyr(p.S259Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000311485
Start	36593140:36593140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1029C>A
AA Mutation	p.Phe343Leu(p.F343L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000311485
Start	36593580:36593580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.589C>T
AA Mutation	p.Leu197Phe(p.L197F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000311485
Start	36593281:36593281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.888G>T
AA Mutation	p.Lys296Asn(p.K296N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000311485
Start	36592645:36592645(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1524delA
AA Mutation	p.Gly509ValfsTer6(p.G509Vfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000311485
Start	36592673:36592673(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1496delA
AA Mutation	p.Lys499SerfsTer4(p.K499Sfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000311485
Start	36593282:36593283(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.886_887insTTTCAAC
AA Mutation	p.Lys296IlefsTer8(p.K296Ifs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	protein_altering_variant
Transcription ID	ENST00000311485
Start	36593750:36593751(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.418_419insTACACT
AA Mutation	p.His140delinsLeuHisTyr(p.H140delinsLHY)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RAG2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311485
Start	36593751:36593751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.418C>A
AA Mutation	p.His140Asn(p.H140N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311485
Start	36592779:36592779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs189020262
CDS Mutation	c.1390C>T
AA Mutation	p.Arg464Cys(p.R464C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript