Colon Cancer: Gene >> BRF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000546474
Start	105228860:105228860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.748A>T
AA Mutation	p.Ile250Phe(p.I250F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000546474
Start	105211218:105211218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777504331
CDS Mutation	c.1900G>A
AA Mutation	p.Val634Met(p.V634M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000546474
Start	105217779:105217779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1537C>T
AA Mutation	p.Arg513Trp(p.R513W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000546474
Start	105286319:105286319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.242C>T
AA Mutation	p.Ser81Leu(p.S81L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000546474
Start	105272868:105272868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.292A>G
AA Mutation	p.Asn98Asp(p.N98D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000546474
Start	105252518:105252518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.533C>T
AA Mutation	p.Ala178Val(p.A178V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000546474
Start	105220088:105220088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1358A>T
AA Mutation	p.Asp453Val(p.D453V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000546474
Start	105241317:105241317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.642G>A
AA Mutation	p.Met214Ile(p.M214I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000546474
Start	105241371:105241371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.588C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000546474
Start	105211165:105211165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1953C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000546474
Start	105228881:105228881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.727A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000546474
Start	105211219:105211219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373154886
CDS Mutation	c.1899C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000546474
Start	105226092:105226092(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1025delG
AA Mutation	p.Gly342AlafsTer36(p.G342Afs*36)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000546474
Start	105226267:105226267(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.939delA
AA Mutation	p.Lys313AsnfsTer20(p.K313Nfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000546474
Start	105226266:105226267(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.939dupA
AA Mutation	p.Leu314ThrfsTer5(p.L314Tfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000546474
Start	105226672:105226673(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs747435524
CDS Mutation	c.876dupC
AA Mutation	p.Ser293LeufsTer15(p.S293Lfs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> BRF1

Mutation ID	1
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000546474
Start	105226673:105226673(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.876delC
AA Mutation	p.Ser293ArgfsTer11(p.S293Rfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000546474
Start	105228866:105228867(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.741_742insA
AA Mutation	p.Glu248ArgfsTer10(p.E248Rfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript