Colon Cancer: Gene >> CSTF3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000323959
Start	33096950:33096950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1157G>A
AA Mutation	p.Arg386Gln(p.R386Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000323959
Start	33096923:33096923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1184G>T
AA Mutation	p.Arg395Ile(p.R395I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000323959
Start	33096956:33096956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1151T>G
AA Mutation	p.Phe384Cys(p.F384C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000323959
Start	33141945:33141945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.69G>T
AA Mutation	p.Lys23Asn(p.K23N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000323959
Start	33103144:33103144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.626G>A
AA Mutation	p.Arg209Gln(p.R209Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323959
Start	33102208:33102208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.795T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323959
Start	33098735:33098735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1083T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323959
Start	33103116:33103116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.654T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000323959
Start	33096364:33096364(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1317delA
AA Mutation	p.Lys439AsnfsTer33(p.K439Nfs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000323959
Start	33102180:33102180(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.823delA
AA Mutation	p.Arg275GlufsTer40(p.R275Efs*40)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000323959
Start	33103156:33103157(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.613dupA
AA Mutation	p.Met205AsnfsTer3(p.M205Nfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000323959
Start	33106056:33106057(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.364dupA
AA Mutation	p.Met122AsnfsTer6(p.M122Nfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000323959
Start	33102253:33102254(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.749_750insAAATTTTAGTAACC
AA Mutation	p.Asp250GlufsTer28(p.D250Efs*28)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CSTF3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000323959
Start	33106024:33106024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.397A>T
AA Mutation	p.Ile133Phe(p.I133F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000323959
Start	33085733:33085733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749330202
CDS Mutation	c.1931G>A
AA Mutation	p.Arg644Gln(p.R644Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323959
Start	33087037:33087037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1746T>A
Mutation Classification	Silent
Feature Type	Transcript