Colon Cancer: Gene >> MAP3K8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263056
Start	30450504:30450504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.751C>A
AA Mutation	p.His251Asn(p.H251N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263056
Start	30460757:30460757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532844555
CDS Mutation	c.1325G>A
AA Mutation	p.Arg442His(p.R442H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263056
Start	30450459:30450459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.706C>T
AA Mutation	p.His236Tyr(p.H236Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263056
Start	30460821:30460821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1389G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263056
Start	30458158:30458158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs114464695
CDS Mutation	c.948G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263056
Start	30450353:30450353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.600T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263056
Start	30458176:30458176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.966G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MAP3K8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263056
Start	30439150:30439150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.212C>A
AA Mutation	p.Pro71Gln(p.P71Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263056
Start	30450311:30450311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.558G>A
Mutation Classification	Silent
Feature Type	Transcript