Colon Cancer: Gene >> MAPK8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374189
Start	48404968:48404968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.239T>G
AA Mutation	p.Val80Gly(p.V80G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374189
Start	48401772:48401772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.112G>C
AA Mutation	p.Gly38Arg(p.G38R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374189
Start	48420255:48420255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.551C>T
AA Mutation	p.Pro184Leu(p.P184L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000374189
Start	48425890:48425890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.691A>G
AA Mutation	p.Ile231Val(p.I231V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374189
Start	48404960:48404960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.231G>T
AA Mutation	p.Met77Ile(p.M77I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000374189
Start	48404853:48404853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200350498
CDS Mutation	c.124G>A
AA Mutation	p.Ala42Thr(p.A42T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000374189
Start	48425977:48425977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.778G>A
AA Mutation	p.Val260Ile(p.V260I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374189
Start	48404867:48404867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.138C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374189
Start	48420253:48420253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367750354
CDS Mutation	c.549G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374189
Start	48420315:48420315(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.614delA
AA Mutation	p.Asn205ThrfsTer45(p.N205Tfs*45)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000374189
Start	48427104:48427104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1021C>T
AA Mutation	p.Gln341Ter(p.Q341*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_lost
Transcription ID	ENST00000374189
Start	48435029:48435029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1284A>G
AA Mutation	p.Ter428TrpextTer17(p.*428Wext*17)
Mutation Classification	Nonstop_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MAPK8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374189
Start	48410061:48410061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.343C>A
AA Mutation	p.Leu115Ile(p.L115I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374189
Start	48409933:48409933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.307G>T
AA Mutation	p.Asp103Tyr(p.D103Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374189
Start	48426467:48426467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.959A>G
AA Mutation	p.Tyr320Cys(p.Y320C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000374189
Start	48424120:48424120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.649G>T
AA Mutation	p.Glu217Ter(p.E217*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript