Colon Cancer: Gene >> AGGF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000312916
Start	77063100:77063100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1993C>T
AA Mutation	p.Pro665Ser(p.P665S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000312916
Start	77059679:77059679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772128053
CDS Mutation	c.1780C>T
AA Mutation	p.Arg594Cys(p.R594C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000312916
Start	77052788:77052788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1448A>C
AA Mutation	p.Asn483Thr(p.N483T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000312916
Start	77055583:77055583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1703A>C
AA Mutation	p.Lys568Thr(p.K568T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000312916
Start	77059710:77059710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1811T>C
AA Mutation	p.Phe604Ser(p.F604S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000312916
Start	77036650:77036650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.611A>C
AA Mutation	p.Gln204Pro(p.Q204P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000312916
Start	77055582:77055582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1702A>C
AA Mutation	p.Lys568Gln(p.K568Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312916
Start	77036571:77036571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.532T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312916
Start	77053988:77053988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753617211
CDS Mutation	c.1491C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312916
Start	77034495:77034495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.288G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000312916
Start	77063142:77063142(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2042delA
AA Mutation	p.Asn681ThrfsTer29(p.N681Tfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000312916
Start	77055543:77055543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1663G>T
AA Mutation	p.Glu555Ter(p.E555*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000312916
Start	77046407:77046407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.931G>T
AA Mutation	p.Glu311Ter(p.E311*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> AGGF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000312916
Start	77039627:77039627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.778C>A
AA Mutation	p.Pro260Thr(p.P260T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000312916
Start	77059710:77059710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1811T>A
AA Mutation	p.Phe604Tyr(p.F604Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000312916
Start	77035729:77035729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.502G>A
AA Mutation	p.Ala168Thr(p.A168T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312916
Start	77059708:77059708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762815931
CDS Mutation	c.1809T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000312916
Start	77063142:77063142(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2042delA
AA Mutation	p.Asn681ThrfsTer29(p.N681Tfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript