Colon Cancer: Gene >> MAS1L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377127
Start	29487776:29487776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.127C>G
AA Mutation	p.Leu43Val(p.L43V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377127
Start	29486978:29486978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139603575
CDS Mutation	c.925G>A
AA Mutation	p.Ala309Thr(p.A309T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377127
Start	29487394:29487394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.509A>G
AA Mutation	p.Glu170Gly(p.E170G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377127
Start	29487112:29487112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145448286
CDS Mutation	c.791C>T
AA Mutation	p.Ala264Val(p.A264V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MAS1L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377127
Start	29486896:29486896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566796111
CDS Mutation	c.1007C>T
AA Mutation	p.Ala336Val(p.A336V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377127
Start	29487786:29487786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.117G>T
AA Mutation	p.Gln39His(p.Q39H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377127
Start	29487031:29487031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.872T>G
AA Mutation	p.Met291Arg(p.M291R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377127
Start	29487588:29487588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757353541
CDS Mutation	c.315G>A
Mutation Classification	Silent
Feature Type	Transcript