Colon Cancer: Gene >> ANGPTL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373425
Start	127108328:127108328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201706693
CDS Mutation	c.404C>T
AA Mutation	p.Thr135Met(p.T135M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373425
Start	127091688:127091688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1264G>T
AA Mutation	p.Asp422Tyr(p.D422Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373425
Start	127108086:127108086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.646C>T
AA Mutation	p.Pro216Ser(p.P216S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373425
Start	127108701:127108701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.31C>A
AA Mutation	p.Leu11Ile(p.L11I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000373425
Start	127093885:127093885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.859G>A
AA Mutation	p.Asp287Asn(p.D287N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000373425
Start	127091766:127091766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143434673
CDS Mutation	c.1186C>T
AA Mutation	p.Arg396Trp(p.R396W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000373425
Start	127108139:127108139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367678181
CDS Mutation	c.593C>T
AA Mutation	p.Ala198Val(p.A198V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000373425
Start	127108542:127108542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs191786568
CDS Mutation	c.190C>T
AA Mutation	p.Arg64Trp(p.R64W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373425
Start	127091763:127091763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1189C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373425
Start	127091907:127091907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1045C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373425
Start	127089059:127089059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139012017
CDS Mutation	c.1362C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373425
Start	127108276:127108276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143084036
CDS Mutation	c.456G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373425
Start	127108390:127108390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201208688
CDS Mutation	c.342C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000373425
Start	127108485:127108485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.247C>T
AA Mutation	p.Arg83Ter(p.R83*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000373425
Start	127089007:127089007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375360881
CDS Mutation	c.1414C>T
AA Mutation	p.Arg472Ter(p.R472*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ANGPTL2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373425
Start	127088960:127088960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138279434
CDS Mutation	c.1461G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373425
Start	127108651:127108651(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.81delT
AA Mutation	p.Phe27LeufsTer15(p.F27Lfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript