Colon Cancer: Gene >> FLI1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000527786
Start	128758298:128758298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754322278
CDS Mutation	c.202C>T
AA Mutation	p.Arg68Trp(p.R68W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000527786
Start	128810587:128810587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.958C>T
AA Mutation	p.Arg320Cys(p.R320C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000527786
Start	128810942:128810942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375383556
CDS Mutation	c.1313G>A
AA Mutation	p.Arg438His(p.R438H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000527786
Start	128772883:128772883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.487G>A
AA Mutation	p.Asp163Asn(p.D163N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000527786
Start	128810686:128810686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1057G>A
AA Mutation	p.Gly353Ser(p.G353S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000527786
Start	128810505:128810505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369798344
CDS Mutation	c.876C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000527786
Start	128768268:128768268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376181944
CDS Mutation	c.381C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000527786
Start	128758192:128758192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs539499213
CDS Mutation	c.96C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000527786
Start	128810625:128810625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752016751
CDS Mutation	c.996C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000527786
Start	128772858:128772858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745359490
CDS Mutation	c.462C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000527786
Start	128758135:128758135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.39C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000527786
Start	128810481:128810481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.852G>A
AA Mutation	p.Trp284Ter(p.W284*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000527786
Start	128805420:128805421(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.710_711insAAGTGT
AA Mutation	p.Gly237_Leu238insSerVal(p.G237_L238insSV)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FLI1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000527786
Start	128810909:128810909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531254948
CDS Mutation	c.1280C>T
AA Mutation	p.Thr427Met(p.T427M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000527786
Start	128807204:128807204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375560426
CDS Mutation	c.746C>T
AA Mutation	p.Thr249Met(p.T249M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000527786
Start	128810693:128810693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1064G>T
AA Mutation	p.Arg355Ile(p.R355I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000527786
Start	128810757:128810757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766521149
CDS Mutation	c.1128G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000527786
Start	128782020:128782020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.652G>T
AA Mutation	p.Glu218Ter(p.E218*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript