Colon Cancer: Gene >> MS4A8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300226
Start	60700868:60700868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8C>T
AA Mutation	p.Ser3Leu(p.S3L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000300226
Start	60715034:60715034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758725009
CDS Mutation	c.548C>T
AA Mutation	p.Ala183Val(p.A183V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300226
Start	60715035:60715035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142632950
CDS Mutation	c.549G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000300226
Start	60708774:60708774(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.530delG
AA Mutation	p.Gly177ValfsTer2(p.G177Vfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000300226
Start	60708733:60708734(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.490dupC
AA Mutation	p.His164ProfsTer82(p.H164Pfs*82)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MS4A8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300226
Start	60700868:60700868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8C>T
AA Mutation	p.Ser3Leu(p.S3L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript