Colon Cancer: Gene >> SF3B2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000322535
Start	66058935:66058935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1072C>A
AA Mutation	p.Arg358Ser(p.R358S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000322535
Start	66058911:66058911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372078828
CDS Mutation	c.1048C>T
AA Mutation	p.Arg350Trp(p.R350W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000322535
Start	66055280:66055280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.463G>T
AA Mutation	p.Ala155Ser(p.A155S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000322535
Start	66055278:66055278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750041004
CDS Mutation	c.461C>T
AA Mutation	p.Ala154Val(p.A154V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000322535
Start	66052392:66052392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8C>T
AA Mutation	p.Thr3Met(p.T3M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000322535
Start	66059951:66059951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1571T>G
AA Mutation	p.Leu524Arg(p.L524R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000322535
Start	66055118:66055118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775280803
CDS Mutation	c.301C>T
AA Mutation	p.Pro101Ser(p.P101S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322535
Start	66055549:66055549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201233817
CDS Mutation	c.513G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322535
Start	66057351:66057351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.753G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322535
Start	66052435:66052435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs556030063
CDS Mutation	c.51G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322535
Start	66061697:66061697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778816554
CDS Mutation	c.1791C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322535
Start	66061941:66061941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1920A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322535
Start	66057297:66057297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.699T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000322535
Start	66068283:66068283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2566G>T
AA Mutation	p.Glu856Ter(p.E856*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SF3B2

Mutation ID	1
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000322535
Start	66055075:66055075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.259-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript