Colon Cancer: Gene >> IHH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295731
Start	219055705:219055705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.738C>A
AA Mutation	p.Phe246Leu(p.F246L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295731
Start	219057507:219057507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.503G>A
AA Mutation	p.Arg168His(p.R168H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295731
Start	219057493:219057493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.517G>A
AA Mutation	p.Ala173Thr(p.A173T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000295731
Start	219060301:219060301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.167T>C
AA Mutation	p.Val56Ala(p.V56A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295731
Start	219057563:219057563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs573679558
CDS Mutation	c.447C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295731
Start	219055399:219055399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775739359
CDS Mutation	c.1044C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295731
Start	219057566:219057566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753939516
CDS Mutation	c.444C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295731
Start	219055308:219055308(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1135delG
AA Mutation	p.Glu379ArgfsTer18(p.E379Rfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295731
Start	219055287:219055287(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1156delC
AA Mutation	p.Gln386SerfsTer11(p.Q386Sfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295731
Start	219055646:219055646(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.797delC
AA Mutation	p.Pro266HisfsTer99(p.P266Hfs*99)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295731
Start	219055683:219055686(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.757_760delAGGC
AA Mutation	p.Arg253Ter(p.R253*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> IHH

Mutation ID	1
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295731
Start	219055544:219055578(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.865_899delCGCTTCCGGGCCACATTTGCCAGCCACGTGCAGCC
AA Mutation	p.Arg289TrpfsTer53(p.R289Wfs*53)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript