Colon Cancer: Gene >> SFI1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000400288
Start	31602616:31602616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1636C>T
AA Mutation	p.His546Tyr(p.H546Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000400288
Start	31531093:31531093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.302G>A
AA Mutation	p.Arg101Gln(p.R101Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000400288
Start	31607940:31607940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2161C>A
AA Mutation	p.Leu721Met(p.L721M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000400288
Start	31604347:31604347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1920G>A
AA Mutation	p.Met640Ile(p.M640I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000400288
Start	31583911:31583911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1285A>C
AA Mutation	p.Ile429Leu(p.I429L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000400288
Start	31602730:31602730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752234090
CDS Mutation	c.1750C>T
AA Mutation	p.Arg584Trp(p.R584W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000400288
Start	31615107:31615107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3128C>T
AA Mutation	p.Thr1043Met(p.T1043M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000400288
Start	31575368:31575368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769372788
CDS Mutation	c.1060C>T
AA Mutation	p.Arg354Cys(p.R354C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000400288
Start	31616758:31616758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759142052
CDS Mutation	c.3314G>A
AA Mutation	p.Arg1105Gln(p.R1105Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000400288
Start	31606421:31606421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2148A>G
AA Mutation	p.Ile716Met(p.I716M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000400288
Start	31614848:31614848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200146787
CDS Mutation	c.3056C>T
AA Mutation	p.Ala1019Val(p.A1019V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000400288
Start	31585093:31585093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757460080
CDS Mutation	c.1372G>A
AA Mutation	p.Glu458Lys(p.E458K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000400288
Start	31546886:31546886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200950795
CDS Mutation	c.364C>T
AA Mutation	p.Arg122Trp(p.R122W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000400288
Start	31615141:31615141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3162G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000400288
Start	31615108:31615108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs557548976
CDS Mutation	c.3129G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000400288
Start	31528850:31528850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.253G>T
AA Mutation	p.Glu85Ter(p.E85*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000400288
Start	31575242:31575242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.934C>T
AA Mutation	p.Arg312Ter(p.R312*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SFI1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000400288
Start	31508290:31508290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6G>T
AA Mutation	p.Lys2Asn(p.K2N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000400288
Start	31546878:31546878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768392322
CDS Mutation	c.356G>A
AA Mutation	p.Arg119Gln(p.R119Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000400288
Start	31531092:31531092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.301C>T
AA Mutation	p.Arg101Ter(p.R101*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript