Colon Cancer: Gene >> MAP4K2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000294066
Start	64791972:64791972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374778757
CDS Mutation	c.2029C>T
AA Mutation	p.Arg677Cys(p.R677C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000294066
Start	64800191:64800191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.833C>A
AA Mutation	p.Pro278His(p.P278H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000294066
Start	64800333:64800333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150751565
CDS Mutation	c.785C>T
AA Mutation	p.Pro262Leu(p.P262L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000294066
Start	64800942:64800942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.620T>C
AA Mutation	p.Leu207Pro(p.L207P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000294066
Start	64799619:64799619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.980C>T
AA Mutation	p.Pro327Leu(p.P327L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000294066
Start	64797358:64797358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1193C>T
AA Mutation	p.Thr398Ile(p.T398I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294066
Start	64796332:64796332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1692A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294066
Start	64792015:64792015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1986G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294066
Start	64796380:64796380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs548385853
CDS Mutation	c.1644G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294066
Start	64802450:64802450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.279C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000294066
Start	64800133:64800133(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.891delC
AA Mutation	p.Ser298ProfsTer38(p.S298Pfs*38)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000294066
Start	64792003:64792004(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1996_1997dupGT
AA Mutation	p.Gly667LeufsTer24(p.G667Lfs*24)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MAP4K2

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000294066
Start	64789623:64789623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2377G>T
AA Mutation	p.Asp793Tyr(p.D793Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript