Colon Cancer: Gene >> PGS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262764
Start	78403673:78403673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.986A>C
AA Mutation	p.Asn329Thr(p.N329T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262764
Start	78400742:78400742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370134635
CDS Mutation	c.767C>T
AA Mutation	p.Ala256Val(p.A256V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262764
Start	78400723:78400723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.748G>A
AA Mutation	p.Val250Met(p.V250M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262764
Start	78399362:78399362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776329786
CDS Mutation	c.526C>T
AA Mutation	p.Arg176Cys(p.R176C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262764
Start	78403780:78403780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1093G>T
AA Mutation	p.Asp365Tyr(p.D365Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262764
Start	78403953:78403953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1266G>T
AA Mutation	p.Lys422Asn(p.K422N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262764
Start	78403671:78403671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.984C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262764
Start	78396337:78396337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757346608
CDS Mutation	c.363C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262764
Start	78392653:78392653(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.321delC
AA Mutation	p.Phe107LeufsTer4(p.F107Lfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262764
Start	78403953:78403953(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1270delG
AA Mutation	p.Val424TrpfsTer60(p.V424Wfs*60)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PGS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262764
Start	78403814:78403814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775469312
CDS Mutation	c.1127C>T
AA Mutation	p.Ala376Val(p.A376V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript