Colon Cancer: Gene >> SF3B1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335508
Start	197392414:197392414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3804T>G
AA Mutation	p.Ile1268Met(p.I1268M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000335508
Start	197405438:197405438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1274G>A
AA Mutation	p.Arg425Gln(p.R425Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000335508
Start	197398518:197398518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3077A>G
AA Mutation	p.Asn1026Ser(p.N1026S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000335508
Start	197409901:197409901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.773C>T
AA Mutation	p.Pro258Leu(p.P258L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000335508
Start	197408564:197408564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.922A>C
AA Mutation	p.Ser308Arg(p.S308R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000335508
Start	197400385:197400385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2768A>G
AA Mutation	p.Lys923Arg(p.K923R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000335508
Start	197398027:197398027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3224G>A
AA Mutation	p.Arg1075Lys(p.R1075K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000335508
Start	197402029:197402029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2179G>T
AA Mutation	p.Val727Leu(p.V727L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000335508
Start	197400388:197400388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2765G>A
AA Mutation	p.Gly922Asp(p.G922D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000335508
Start	197393153:197393153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3575T>C
AA Mutation	p.Val1192Ala(p.V1192A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000335508
Start	197402085:197402085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2123C>T
AA Mutation	p.Ala708Val(p.A708V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000335508
Start	197408048:197408048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1189C>T
AA Mutation	p.Arg397Cys(p.R397C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000335508
Start	197402044:197402044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2164G>A
AA Mutation	p.Glu722Lys(p.E722K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000335508
Start	197416811:197416811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.596G>A
AA Mutation	p.Arg199His(p.R199H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000335508
Start	197398496:197398496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3099G>T
AA Mutation	p.Glu1033Asp(p.E1033D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000335508
Start	197393145:197393145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3583A>G
AA Mutation	p.Met1195Val(p.M1195V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000335508
Start	197398032:197398032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3219T>G
AA Mutation	p.Ile1073Met(p.I1073M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000335508
Start	197423957:197423957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.46C>G
AA Mutation	p.Arg16Gly(p.R16G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000335508
Start	197423857:197423857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.146G>T
AA Mutation	p.Ser49Ile(p.S49I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335508
Start	197409825:197409825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747909166
CDS Mutation	c.849C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335508
Start	197403015:197403015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566175207
CDS Mutation	c.1740G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000335508
Start	197401451:197401451(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2445delT
AA Mutation	p.Phe815LeufsTer19(p.F815Lfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SF3B1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335508
Start	197408542:197408542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.944G>A
AA Mutation	p.Arg315Gln(p.R315Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000335508
Start	197423903:197423903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.100G>A
AA Mutation	p.Asp34Asn(p.D34N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript