Colon Cancer: Gene >> MAP2K4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000353533
Start	12113301:12113301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.754G>A
AA Mutation	p.Gly252Arg(p.G252R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000353533
Start	12125340:12125340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.860G>A
AA Mutation	p.Arg287His(p.R287H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000353533
Start	12110397:12110397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.656T>C
AA Mutation	p.Leu219Ser(p.L219S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000353533
Start	12081433:12081433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.296C>T
AA Mutation	p.Ala99Val(p.A99V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000353533
Start	12129224:12129224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267604739
CDS Mutation	c.977C>T
AA Mutation	p.Pro326Leu(p.P326L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000353533
Start	12141151:12141151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1091A>C
AA Mutation	p.His364Pro(p.H364P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000353533
Start	12107875:12107875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.599T>C
AA Mutation	p.Ile200Thr(p.I200T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000353533
Start	12125353:12125353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.873G>T
AA Mutation	p.Trp291Cys(p.W291C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000353533
Start	12129164:12129164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.917C>A
AA Mutation	p.Pro306His(p.P306H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000353533
Start	12095581:12095581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.400C>T
AA Mutation	p.Arg134Trp(p.R134W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000353533
Start	12081424:12081424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.287A>T
AA Mutation	p.Asp96Val(p.D96V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000353533
Start	12110385:12110385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.644C>G
AA Mutation	p.Ala215Gly(p.A215G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000353533
Start	12081376:12081376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.239G>A
AA Mutation	p.Ser80Asn(p.S80N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000353533
Start	12125351:12125351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.871T>C
AA Mutation	p.Trp291Arg(p.W291R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000353533
Start	12139844:12139844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755523599
CDS Mutation	c.1046C>T
AA Mutation	p.Thr349Met(p.T349M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000353533
Start	12095602:12095602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.421G>A
AA Mutation	p.Glu141Lys(p.E141K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000353533
Start	12129283:12129283(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1037delT
AA Mutation	p.Leu346CysfsTer17(p.L346Cfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000353533
Start	12113287:12113290(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.740_743delACTT
AA Mutation	p.Asp247AlafsTer28(p.D247Afs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000353533
Start	12081456:12081456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.319G>T
AA Mutation	p.Glu107Ter(p.E107*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000353533
Start	12095602:12095602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.421G>T
AA Mutation	p.Glu141Ter(p.E141*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000353533
Start	12107883:12107883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.607G>T
AA Mutation	p.Glu203Ter(p.E203*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000353533
Start	12125297:12125297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.817G>T
AA Mutation	p.Glu273Ter(p.E273*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000353533
Start	12110374:12110374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.634-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000353533
Start	12139837:12139837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1041-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000353533
Start	12113290:12113295(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.745_750delGGCATC
AA Mutation	p.Gly249_Ile250del(p.G249_I250del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MAP2K4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000353533
Start	12095581:12095581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.400C>T
AA Mutation	p.Arg134Trp(p.R134W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000353533
Start	12113304:12113304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.757C>T
AA Mutation	p.Gln253Ter(p.Q253*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000353533
Start	12125293:12125293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.814-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript