Colon Cancer: Gene >> SF3A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000215793
Start	30339213:30339213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1414C>T
AA Mutation	p.Arg472Trp(p.R472W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000215793
Start	30340282:30340282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1289G>A
AA Mutation	p.Arg430His(p.R430H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000215793
Start	30341876:30341876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.887C>A
AA Mutation	p.Pro296His(p.P296H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000215793
Start	30337737:30337737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377475726
CDS Mutation	c.1904C>T
AA Mutation	p.Ala635Val(p.A635V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000215793
Start	30339130:30339130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1497G>T
AA Mutation	p.Lys499Asn(p.K499N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000215793
Start	30345075:30345075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370505540
CDS Mutation	c.509C>T
AA Mutation	p.Thr170Met(p.T170M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000215793
Start	30346477:30346477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.228C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000215793
Start	30338837:30338837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1695C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000215793
Start	30338858:30338858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771207177
CDS Mutation	c.1674G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000215793
Start	30337717:30337717(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1924delC
AA Mutation	p.Arg642AlafsTer5(p.R642Afs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SF3A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000215793
Start	30339180:30339180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1447G>A
AA Mutation	p.Ala483Thr(p.A483T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript