Colon Cancer: Gene >> LCK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336890
Start	32276400:32276400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.695C>T
AA Mutation	p.Pro232Leu(p.P232L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336890
Start	32276370:32276370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749760246
CDS Mutation	c.665G>A
AA Mutation	p.Arg222His(p.R222H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000336890
Start	32276727:32276727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.905G>A
AA Mutation	p.Arg302Gln(p.R302Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000336890
Start	32279876:32279876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1077T>A
AA Mutation	p.Asn359Lys(p.N359K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000336890
Start	32274785:32274785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.154G>A
AA Mutation	p.Glu52Lys(p.E52K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336890
Start	32276671:32276671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760860694
CDS Mutation	c.849C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> LCK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336890
Start	32275929:32275929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.497C>T
AA Mutation	p.Ser166Leu(p.S166L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336890
Start	32275399:32275399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778915733
CDS Mutation	c.357G>A
Mutation Classification	Silent
Feature Type	Transcript