Colon Cancer: Gene >> DUSP9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000342782
Start	153649399:153649399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781805190
CDS Mutation	c.541G>A
AA Mutation	p.Asp181Asn(p.D181N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000342782
Start	153650253:153650253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1103C>A
AA Mutation	p.Ser368Tyr(p.S368Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000342782
Start	153649683:153649683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.825C>A
AA Mutation	p.Phe275Leu(p.F275L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000342782
Start	153649333:153649333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782644901
CDS Mutation	c.475G>A
AA Mutation	p.Val159Met(p.V159M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000342782
Start	153647991:153647991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.38G>A
AA Mutation	p.Arg13Gln(p.R13Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342782
Start	153649386:153649386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.528C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000342782
Start	153650219:153650219(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1074delG
AA Mutation	p.Gln359ArgfsTer77(p.Q359Rfs*77)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DUSP9

No Mutation Annotation!