Colon Cancer: Gene >> TP53INP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000342697
Start	94930553:94930553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.649G>A
AA Mutation	p.Asp217Asn(p.D217N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000342697
Start	94939896:94939896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532052124
CDS Mutation	c.437G>A
AA Mutation	p.Arg146His(p.R146H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000342697
Start	94940194:94940194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.139G>A
AA Mutation	p.Glu47Lys(p.E47K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000342697
Start	94930570:94930570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.632G>A
AA Mutation	p.Arg211His(p.R211H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342697
Start	94930629:94930629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.573T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342697
Start	94940183:94940183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs548441545
CDS Mutation	c.150A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342697
Start	94930521:94930521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.681C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000342697
Start	94930652:94930653(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.549_550insAT
AA Mutation	p.Glu184MetfsTer13(p.E184Mfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TP53INP1

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000342697
Start	94930613:94930613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.589G>T
AA Mutation	p.Glu197Ter(p.E197*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript