Colon Cancer: Gene >> CTSH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000220166
Start	78944948:78944948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs543936667
CDS Mutation	c.34G>A
AA Mutation	p.Ala12Thr(p.A12T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000220166
Start	78932395:78932395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.469G>A
AA Mutation	p.Ala157Thr(p.A157T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000220166
Start	78931473:78931473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.526T>C
AA Mutation	p.Phe176Leu(p.F176L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000220166
Start	78925434:78925434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747510233
CDS Mutation	c.706G>A
AA Mutation	p.Glu236Lys(p.E236K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000220166
Start	78931482:78931482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.517G>A
AA Mutation	p.Ala173Thr(p.A173T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000220166
Start	78925417:78925417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.723G>T
AA Mutation	p.Glu241Asp(p.E241D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000220166
Start	78923050:78923050(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.875delA
AA Mutation	p.Asn292MetfsTer8(p.N292Mfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000220166
Start	78923049:78923050(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.875dupA
AA Mutation	p.Asn292LysfsTer119(p.N292Kfs*119)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CTSH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000220166
Start	78925391:78925391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.749G>A
AA Mutation	p.Ser250Asn(p.S250N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript