Colon Cancer: Gene >> MAP3K1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000399503
Start	56893600:56893600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4459C>T
AA Mutation	p.Arg1487Cys(p.R1487C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000399503
Start	56881153:56881153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2250T>A
AA Mutation	p.Asn750Lys(p.N750K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000399503
Start	56872653:56872653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1436G>C
AA Mutation	p.Cys479Ser(p.C479S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000399503
Start	56865353:56865353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1049C>T
AA Mutation	p.Ala350Val(p.A350V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000399503
Start	56865356:56865356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765046318
CDS Mutation	c.1052G>A
AA Mutation	p.Arg351His(p.R351H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000399503
Start	56882228:56882228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3028A>G
AA Mutation	p.Ile1010Val(p.I1010V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000399503
Start	56883589:56883589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3729G>T
AA Mutation	p.Trp1243Cys(p.W1243C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000399503
Start	56881817:56881817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149242419
CDS Mutation	c.2617G>A
AA Mutation	p.Val873Ile(p.V873I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000399503
Start	56875050:56875050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1705G>A
AA Mutation	p.Val569Ile(p.V569I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000399503
Start	56884824:56884824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3980C>T
AA Mutation	p.Ala1327Val(p.A1327V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000399503
Start	56885938:56885938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3989C>T
AA Mutation	p.Ser1330Leu(p.S1330L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000399503
Start	56881107:56881107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2204A>T
AA Mutation	p.Asp735Val(p.D735V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000399503
Start	56887450:56887450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4187C>T
AA Mutation	p.Ala1396Val(p.A1396V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000399503
Start	56888283:56888283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4315A>T
AA Mutation	p.Ile1439Phe(p.I1439F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000399503
Start	56875093:56875093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1748C>T
AA Mutation	p.Ala583Val(p.A583V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000399503
Start	56859824:56859824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201579608
CDS Mutation	c.743G>A
AA Mutation	p.Arg248Gln(p.R248Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000399503
Start	56864816:56864816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375262853
CDS Mutation	c.917G>A
AA Mutation	p.Arg306His(p.R306H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000399503
Start	56875053:56875053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1708G>T
AA Mutation	p.Gly570Cys(p.G570C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000399503
Start	56893532:56893532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4391T>G
AA Mutation	p.Ile1464Ser(p.I1464S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399503
Start	56875298:56875298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199816039
CDS Mutation	c.1953C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000399503
Start	56865944:56865944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1268C>A
AA Mutation	p.Ser423Ter(p.S423*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000399503
Start	56884775:56884775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3931G>T
AA Mutation	p.Gly1311Ter(p.G1311*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000399503
Start	56856708:56856708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747386435
CDS Mutation	c.591G>A
AA Mutation	p.Trp197Ter(p.W197*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000399503
Start	56856739:56856739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.622C>T
AA Mutation	p.Arg208Ter(p.R208*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MAP3K1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000399503
Start	56885938:56885938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3989C>T
AA Mutation	p.Ser1330Leu(p.S1330L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000399503
Start	56872704:56872704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1487G>T
AA Mutation	p.Arg496Ile(p.R496I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000399503
Start	56881166:56881166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2263C>A
AA Mutation	p.Leu755Ile(p.L755I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000399503
Start	56879028:56879028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2014G>T
AA Mutation	p.Glu672Ter(p.E672*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript