Colon Cancer: Gene >> DOK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000233668
Start	74556974:74556974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1306G>A
AA Mutation	p.Ala436Thr(p.A436T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000233668
Start	74556693:74556693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1025A>G
AA Mutation	p.Glu342Gly(p.E342G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000233668
Start	74556071:74556071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370948984
CDS Mutation	c.632G>A
AA Mutation	p.Arg211Gln(p.R211Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000233668
Start	74555932:74555932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756157059
CDS Mutation	c.493G>A
AA Mutation	p.Ala165Thr(p.A165T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000233668
Start	74555314:74555314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.221C>T
AA Mutation	p.Ala74Val(p.A74V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000233668
Start	74556879:74556879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753672963
CDS Mutation	c.1211C>T
AA Mutation	p.Pro404Leu(p.P404L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000233668
Start	74556044:74556044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.605C>A
AA Mutation	p.Pro202His(p.P202H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000233668
Start	74556950:74556950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1282C>A
AA Mutation	p.Pro428Thr(p.P428T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233668
Start	74556319:74556319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.651T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000233668
Start	74554783:74554783(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.35delT
AA Mutation	p.Leu12CysfsTer26(p.L12Cfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000233668
Start	74555439:74555439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.346C>T
AA Mutation	p.Arg116Ter(p.R116*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> DOK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000233668
Start	74555640:74555640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.426G>T
AA Mutation	p.Glu142Asp(p.E142D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript