Colon Cancer: Gene >> DOK3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357198
Start	177508502:177508502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.275G>A
AA Mutation	p.Gly92Asp(p.G92D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357198
Start	177504826:177504826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376073825
CDS Mutation	c.730G>A
AA Mutation	p.Ala244Thr(p.A244T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000357198
Start	177508463:177508463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758932270
CDS Mutation	c.314G>A
AA Mutation	p.Arg105Gln(p.R105Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000357198
Start	177504336:177504336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1138C>T
AA Mutation	p.Leu380Phe(p.L380F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000357198
Start	177504171:177504171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1303G>A
AA Mutation	p.Gly435Ser(p.G435S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000357198
Start	177504462:177504462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs577271160
CDS Mutation	c.1012G>A
AA Mutation	p.Gly338Arg(p.G338R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000357198
Start	177504200:177504200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1274G>T
AA Mutation	p.Ser425Ile(p.S425I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000357198
Start	177508485:177508485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777637154
CDS Mutation	c.292C>T
AA Mutation	p.Arg98Trp(p.R98W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357198
Start	177504622:177504622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374290190
CDS Mutation	c.852G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> DOK3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357198
Start	177504886:177504886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.670A>G
AA Mutation	p.Thr224Ala(p.T224A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357198
Start	177504755:177504755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374194442
CDS Mutation	c.801C>T
Mutation Classification	Silent
Feature Type	Transcript