Colon Cancer: Gene >> MAP4K5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000013125
Start	50486182:50486182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.179C>A
AA Mutation	p.Ser60Tyr(p.S60Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000013125
Start	50462700:50462700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368497445
CDS Mutation	c.901G>A
AA Mutation	p.Ala301Thr(p.A301T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000013125
Start	50425936:50425936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2368A>G
AA Mutation	p.Met790Val(p.M790V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000013125
Start	50423140:50423140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2434C>T
AA Mutation	p.Arg812Cys(p.R812C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000013125
Start	50531959:50531959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.91T>C
AA Mutation	p.Tyr31His(p.Y31H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000013125
Start	50429213:50429213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2212A>G
AA Mutation	p.Thr738Ala(p.T738A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000013125
Start	50434553:50434553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2005C>T
AA Mutation	p.Pro669Ser(p.P669S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000013125
Start	50485603:50485603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751262314
CDS Mutation	c.297C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000013125
Start	50464078:50464078(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs772316463
CDS Mutation	c.793delA
AA Mutation	p.Arg265AspfsTer8(p.R265Dfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MAP4K5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000013125
Start	50486189:50486189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.172G>T
AA Mutation	p.Asp58Tyr(p.D58Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript