Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ANGPT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000517746
Start	107347007:107347007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.388A>T
AA Mutation	p.Ile130Leu(p.I130L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000517746
Start	107303280:107303280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.896T>C
AA Mutation	p.Ile299Thr(p.I299T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000517746
Start	107497515:107497515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.44C>T
AA Mutation	p.Thr15Ile(p.T15I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000517746
Start	107347066:107347066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.329C>T
AA Mutation	p.Ser110Leu(p.S110L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000517746
Start	107293948:107293948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1026G>T
AA Mutation	p.Lys342Asn(p.K342N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000517746
Start	107497284:107497284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.275A>C
AA Mutation	p.Asn92Thr(p.N92T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000517746
Start	107497350:107497351(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.208_209delGA
AA Mutation	p.Asp70CysfsTer31(p.D70Cfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000517746
Start	107497480:107497480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.79G>T
AA Mutation	p.Glu27Ter(p.E27*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ANGPT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000517746
Start	107497450:107497450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.109C>A
AA Mutation	p.Gln37Lys(p.Q37K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000517746
Start	107303364:107303364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.812T>C
AA Mutation	p.Leu271Ser(p.L271S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000517746
Start	107347094:107347094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.301G>A
AA Mutation	p.Glu101Lys(p.E101K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000517746
Start	107497385:107497385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.174G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000517746
Start	107251960:107251960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1392G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000517746
Start	107322044:107322044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.660A>G
Mutation Classification	Silent
Feature Type	Transcript