Colon Cancer: Gene >> ANGPTL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000234816
Start	178865636:178865636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.141G>T
AA Mutation	p.Lys47Asn(p.K47N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000234816
Start	178852778:178852778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs570797031
CDS Mutation	c.1193G>A
AA Mutation	p.Arg398His(p.R398H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000234816
Start	178865626:178865626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.151T>C
AA Mutation	p.Tyr51His(p.Y51H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000234816
Start	178865400:178865400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371498898
CDS Mutation	c.377T>C
AA Mutation	p.Met126Thr(p.M126T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000234816
Start	178865529:178865529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.248T>C
AA Mutation	p.Met83Thr(p.M83T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000234816
Start	178865374:178865374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.403A>G
AA Mutation	p.Met135Val(p.M135V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000234816
Start	178865746:178865746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.31C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000234816
Start	178865240:178865240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs546016893
CDS Mutation	c.537C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000234816
Start	178865567:178865567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.210G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000234816
Start	178865159:178865159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.618A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000234816
Start	178865161:178865161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748411414
CDS Mutation	c.616C>T
AA Mutation	p.Arg206Ter(p.R206*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000234816
Start	178853660:178853661(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.950dupG
AA Mutation	p.Trp318LeufsTer22(p.W318Lfs*22)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ANGPTL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000234816
Start	178865285:178865285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.492A>C
AA Mutation	p.Glu164Asp(p.E164D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000234816
Start	178865554:178865554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.223A>G
AA Mutation	p.Thr75Ala(p.T75A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000234816
Start	178865673:178865673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.104G>T
AA Mutation	p.Arg35Ile(p.R35I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript