Colon Cancer: Gene >> STOML3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379631
Start	38972552:38972552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.272T>C
AA Mutation	p.Val91Ala(p.V91A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379631
Start	38968459:38968459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs575718463
CDS Mutation	c.592G>A
AA Mutation	p.Val198Met(p.V198M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379631
Start	38966936:38966936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758784714
CDS Mutation	c.765G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> STOML3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379631
Start	38970255:38970255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.446G>T
AA Mutation	p.Arg149Ile(p.R149I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379631
Start	38968416:38968416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755648849
CDS Mutation	c.635G>A
AA Mutation	p.Arg212Gln(p.R212Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379631
Start	38968513:38968513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753468566
CDS Mutation	c.538G>A
AA Mutation	p.Glu180Lys(p.E180K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000379631
Start	38970203:38970203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.498G>T
AA Mutation	p.Glu166Asp(p.E166D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379631
Start	38966867:38966867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748546865
CDS Mutation	c.834C>T
Mutation Classification	Silent
Feature Type	Transcript