Colon Cancer: Gene >> CTSL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340342
Start	87728733:87728733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.545T>C
AA Mutation	p.Leu182Pro(p.L182P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340342
Start	87728730:87728730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.542G>A
AA Mutation	p.Gly181Asp(p.G181D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000340342
Start	87728638:87728638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.450G>T
AA Mutation	p.Gln150His(p.Q150H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000340342
Start	87731061:87731061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.956G>T
AA Mutation	p.Arg319Ile(p.R319I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340342
Start	87728384:87728384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.384T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340342
Start	87729620:87729620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs570819883
CDS Mutation	c.669C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340342
Start	87730445:87730445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs190277186
CDS Mutation	c.849C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340342
Start	87727693:87727693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.90C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000340342
Start	87728259:87728259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.259G>T
AA Mutation	p.Glu87Ter(p.E87*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CTSL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340342
Start	87729725:87729725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.774C>A
AA Mutation	p.Phe258Leu(p.F258L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340342
Start	87727723:87727723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs546059099
CDS Mutation	c.120C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000340342
Start	87729590:87729590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.639C>G
AA Mutation	p.Tyr213Ter(p.Y213*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript