Colon Cancer: Gene >> TRIM68

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300747
Start	4601119:4601119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.815C>T
AA Mutation	p.Ser272Phe(p.S272F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000300747
Start	4605206:4605206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758373806
CDS Mutation	c.299G>A
AA Mutation	p.Arg100His(p.R100H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000300747
Start	4602311:4602311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.624G>T
AA Mutation	p.Glu208Asp(p.E208D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000300747
Start	4605207:4605207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777719012
CDS Mutation	c.298C>T
AA Mutation	p.Arg100Cys(p.R100C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000300747
Start	4600707:4600707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199878371
CDS Mutation	c.1027C>T
AA Mutation	p.Arg343Cys(p.R343C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000300747
Start	4600588:4600588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1146G>T
AA Mutation	p.Lys382Asn(p.K382N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300747
Start	4600696:4600696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1038C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000300747
Start	4600566:4600566(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1168delC
AA Mutation	p.His390ThrfsTer6(p.H390Tfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000300747
Start	4605354:4605355(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.150_151insTCTTTG
AA Mutation	p.Ser50_Gln51insSerLeu(p.S50_Q51insSL)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TRIM68

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300747
Start	4601072:4601072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.862G>C
AA Mutation	p.Asp288His(p.D288H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript