Colon Cancer: Gene >> BRF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000220659
Start	37846893:37846893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140725525
CDS Mutation	c.497C>T
AA Mutation	p.Ser166Phe(p.S166F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000220659
Start	37846885:37846885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.505T>G
AA Mutation	p.Leu169Val(p.L169V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000220659
Start	37847067:37847067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372281989
CDS Mutation	c.323C>T
AA Mutation	p.Ala108Val(p.A108V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000220659
Start	37844936:37844936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.814G>A
AA Mutation	p.Val272Met(p.V272M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000220659
Start	37846855:37846855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.535A>T
AA Mutation	p.Ser179Cys(p.S179C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220659
Start	37849763:37849763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.21C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220659
Start	37845078:37845078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372185215
CDS Mutation	c.672C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220659
Start	37844496:37844496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1254T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220659
Start	37844802:37844802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.948A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000220659
Start	37844629:37844629(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1121delC
AA Mutation	p.Pro374LeufsTer16(p.P374Lfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000220659
Start	37849668:37849669(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.115dupG
AA Mutation	p.Val39GlyfsTer28(p.V39Gfs*28)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> BRF2

Mutation ID	1
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000220659
Start	37845057:37845058(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.692dupT
AA Mutation	p.Leu232ProfsTer21(p.L232Pfs*21)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript