Colon Cancer: Gene >> MKKS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000347364
Start	10412884:10412884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.631G>T
AA Mutation	p.Asp211Tyr(p.D211Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000347364
Start	10408732:10408732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1057G>A
AA Mutation	p.Ala353Thr(p.A353T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000347364
Start	10413280:10413280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750058438
CDS Mutation	c.235G>A
AA Mutation	p.Ala79Thr(p.A79T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347364
Start	10405466:10405466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769705805
CDS Mutation	c.1494C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347364
Start	10405445:10405445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1515G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MKKS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000347364
Start	10405371:10405371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1589C>T
AA Mutation	p.Ala530Val(p.A530V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000347364
Start	10413192:10413192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.323G>A
AA Mutation	p.Arg108Lys(p.R108K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript