Colon Cancer: Gene >> DUSP5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369583
Start	110498212:110498212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.91T>C
AA Mutation	p.Tyr31His(p.Y31H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369583
Start	110507046:110507046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144264318
CDS Mutation	c.640C>T
AA Mutation	p.Arg214Trp(p.R214W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369583
Start	110510211:110510211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775205143
CDS Mutation	c.940G>A
AA Mutation	p.Glu314Lys(p.E314K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369583
Start	110510347:110510347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141147474
CDS Mutation	c.1076C>T
AA Mutation	p.Ser359Leu(p.S359L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369583
Start	110506991:110506991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.585C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369583
Start	110507003:110507003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749989755
CDS Mutation	c.597C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000369583
Start	110510196:110510198(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.926_928delAGC
AA Mutation	p.Gln309del(p.Q309del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DUSP5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369583
Start	110507083:110507083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.677A>C
AA Mutation	p.Lys226Thr(p.K226T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript