Colon Cancer: Gene >> MS4A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000278888
Start	60093995:60093995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.569T>C
AA Mutation	p.Ile190Thr(p.I190T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000278888
Start	60094018:60094018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.592T>C
AA Mutation	p.Ser198Pro(p.S198P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000278888
Start	60095582:60095582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.661G>T
AA Mutation	p.Glu221Ter(p.E221*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MS4A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000278888
Start	60092834:60092834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.364A>T
AA Mutation	p.Asn122Tyr(p.N122Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278888
Start	60089815:60089815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267603048
CDS Mutation	c.180C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000278888
Start	60094045:60094045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.619G>T
AA Mutation	p.Glu207Ter(p.E207*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000278888
Start	60089797:60089798(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.168dupA
AA Mutation	p.Glu57ArgfsTer28(p.E57Rfs*28)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript