Colon Cancer: Gene >> MAPK9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000452135
Start	180238386:180238386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1078G>C
AA Mutation	p.Val360Leu(p.V360L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000452135
Start	180242692:180242692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.752A>C
AA Mutation	p.Lys251Thr(p.K251T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000452135
Start	180261689:180261689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.445C>A
AA Mutation	p.His149Asn(p.H149N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000452135
Start	180242729:180242729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.715G>A
AA Mutation	p.Glu239Lys(p.E239K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000452135
Start	180280542:180280542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.20A>G
AA Mutation	p.Asp7Gly(p.D7G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MAPK9

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000452135
Start	180242588:180242588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373601817
CDS Mutation	c.856C>T
AA Mutation	p.Arg286Ter(p.R286*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_lost
Transcription ID	ENST00000452135
Start	180236384:180236384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1275A>C
AA Mutation	p.Ter425CysextTer1(p.*425Cext*1)
Mutation Classification	Nonstop_Mutation
Feature Type	Transcript