Colon Cancer: Gene >> MAP3K3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361733
Start	63690344:63690344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1144G>A
AA Mutation	p.Val382Met(p.V382M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361733
Start	63690356:63690356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756808678
CDS Mutation	c.1156C>T
AA Mutation	p.Arg386Cys(p.R386C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361733
Start	63692305:63692305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1538G>A
AA Mutation	p.Arg513His(p.R513H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361733
Start	63689666:63689666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766496256
CDS Mutation	c.994C>T
AA Mutation	p.Arg332Cys(p.R332C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000361733
Start	63646074:63646074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.167G>A
AA Mutation	p.Arg56Gln(p.R56Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361733
Start	63681796:63681796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749547349
CDS Mutation	c.533C>T
AA Mutation	p.Pro178Leu(p.P178L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361733
Start	63691161:63691161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768423193
CDS Mutation	c.1272C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361733
Start	63666999:63666999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202050738
CDS Mutation	c.441C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000361733
Start	63685592:63685592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.710+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> MAP3K3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361733
Start	63646044:63646044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.137G>A
AA Mutation	p.Arg46Lys(p.R46K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361733
Start	63693556:63693556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1660G>A
AA Mutation	p.Gly554Ser(p.G554S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript