Colon Cancer: Gene >> MOK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361847
Start	102232590:102232590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.811G>A
AA Mutation	p.Asp271Asn(p.D271N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361847
Start	102232578:102232578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754455482
CDS Mutation	c.823G>A
AA Mutation	p.Ala275Thr(p.A275T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361847
Start	102229549:102229549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1090T>A
AA Mutation	p.Ser364Thr(p.S364T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361847
Start	102229323:102229323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1226G>A
AA Mutation	p.Arg409His(p.R409H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361847
Start	102263588:102263588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.241A>C
AA Mutation	p.Ile81Leu(p.I81L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361847
Start	102229590:102229590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1049C>T
AA Mutation	p.Pro350Leu(p.P350L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000361847
Start	102232707:102232707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.694T>C
AA Mutation	p.Ser232Pro(p.S232P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361847
Start	102231770:102231770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.918G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361847
Start	102250862:102250862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367966130
CDS Mutation	c.540G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361847
Start	102229334:102229334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774153346
CDS Mutation	c.1215G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361847
Start	102229361:102229361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1188T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361847
Start	102250817:102250817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199967642
CDS Mutation	c.585C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361847
Start	102233774:102233775(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.605_606insGG
AA Mutation	p.Phe202LeufsTer5(p.F202Lfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MOK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361847
Start	102263586:102263586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.243A>G
AA Mutation	p.Ile81Met(p.I81M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript