Colon Cancer: Gene >> FCGRT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000221466
Start	49514432:49514432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373482955
CDS Mutation	c.547C>T
AA Mutation	p.Pro183Ser(p.P183S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000221466
Start	49514351:49514351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.466G>A
AA Mutation	p.Glu156Lys(p.E156K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000221466
Start	49525501:49525501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144900355
CDS Mutation	c.916G>A
AA Mutation	p.Gly306Ser(p.G306S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000221466
Start	49514241:49514241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.356G>T
AA Mutation	p.Cys119Phe(p.C119F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000221466
Start	49524744:49524744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777748221
CDS Mutation	c.839C>T
AA Mutation	p.Ala280Val(p.A280V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000221466
Start	49525502:49525502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.917G>T
AA Mutation	p.Gly306Val(p.G306V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221466
Start	49513406:49513406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221466
Start	49524532:49524532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.627C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221466
Start	49524754:49524754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761660729
CDS Mutation	c.849G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000221466
Start	49514123:49514123(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.320delG
AA Mutation	p.Gly107GlufsTer29(p.G107Efs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> FCGRT

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000221466
Start	49514476:49514476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.591G>A
Mutation Classification	Silent
Feature Type	Transcript