Colon Cancer: Gene >> MAP4K1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000591517
Start	38605424:38605424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1431A>C
AA Mutation	p.Glu477Asp(p.E477D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000591517
Start	38611130:38611130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.731C>T
AA Mutation	p.Ser244Leu(p.S244L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000591517
Start	38596414:38596414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2014G>A
AA Mutation	p.Ala672Thr(p.A672T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000591517
Start	38596353:38596353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2075G>A
AA Mutation	p.Arg692His(p.R692H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000591517
Start	38597517:38597517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750447520
CDS Mutation	c.1747G>A
AA Mutation	p.Ala583Thr(p.A583T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000591517
Start	38595694:38595694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2215G>T
AA Mutation	p.Val739Phe(p.V739F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000591517
Start	38595691:38595691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2218C>T
AA Mutation	p.Arg740Trp(p.R740W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000591517
Start	38593319:38593319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2359G>T
AA Mutation	p.Asp787Tyr(p.D787Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000591517
Start	38609947:38609947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.889G>C
AA Mutation	p.Gly297Arg(p.G297R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000591517
Start	38612657:38612657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.619G>A
AA Mutation	p.Glu207Lys(p.E207K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000591517
Start	38605465:38605465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1390C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000591517
Start	38616226:38616226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.282T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000591517
Start	38605665:38605665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs560515565
CDS Mutation	c.1266G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MAP4K1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000591517
Start	38597089:38597089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1886C>A
AA Mutation	p.Thr629Lys(p.T629K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000591517
Start	38611301:38611301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.670C>A
AA Mutation	p.Leu224Ile(p.L224I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000591517
Start	38612634:38612634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs35922303
CDS Mutation	c.642G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000591517
Start	38606176:38606180(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1193_1197delCCCCC
AA Mutation	p.Pro398GlnfsTer18(p.P398Qfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000591517
Start	38611077:38611077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.784C>T
AA Mutation	p.Arg262Ter(p.R262*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript