Colon Cancer: Gene >> DOK5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262593
Start	54650457:54650457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.899C>G
AA Mutation	p.Pro300Arg(p.P300R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262593
Start	54643552:54643552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.830G>A
AA Mutation	p.Ser277Asn(p.S277N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262593
Start	54643542:54643542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749182201
CDS Mutation	c.820C>T
AA Mutation	p.Arg274Trp(p.R274W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262593
Start	54650442:54650442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142008881
CDS Mutation	c.884G>A
AA Mutation	p.Arg295Gln(p.R295Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262593
Start	54588738:54588738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.341C>T
AA Mutation	p.Thr114Ile(p.T114I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262593
Start	54588489:54588489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.181G>A
AA Mutation	p.Glu61Lys(p.E61K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262593
Start	54475966:54475966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.20A>G
AA Mutation	p.Asp7Gly(p.D7G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262593
Start	54555035:54555035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.169C>A
AA Mutation	p.His57Asn(p.H57N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000262593
Start	54588740:54588740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773975138
CDS Mutation	c.343C>T
AA Mutation	p.Arg115Trp(p.R115W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000262593
Start	54588737:54588737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.340A>G
AA Mutation	p.Thr114Ala(p.T114A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000262593
Start	54588779:54588779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.382G>T
AA Mutation	p.Ala128Ser(p.A128S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000262593
Start	54650457:54650457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.899C>A
AA Mutation	p.Pro300Gln(p.P300Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262593
Start	54588590:54588590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144328268
CDS Mutation	c.282C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262593
Start	54591665:54591665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762067549
CDS Mutation	c.459C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000262593
Start	54591690:54591690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.484G>T
AA Mutation	p.Glu162Ter(p.E162*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> DOK5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262593
Start	54591763:54591763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769217160
CDS Mutation	c.557G>A
AA Mutation	p.Arg186Gln(p.R186Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000262593
Start	54588489:54588489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.181G>T
AA Mutation	p.Glu61Ter(p.E61*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript