Colon Cancer: Gene >> ANGPT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325203
Start	6514738:6514738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.971T>A
AA Mutation	p.Ile324Asn(p.I324N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000325203
Start	6562867:6562867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.68G>A
AA Mutation	p.Arg23Gln(p.R23Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000325203
Start	6503223:6503223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1369G>A
AA Mutation	p.Gly457Arg(p.G457R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000325203
Start	6527612:6527612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.509T>C
AA Mutation	p.Leu170Ser(p.L170S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000325203
Start	6527631:6527631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.490T>C
AA Mutation	p.Ser164Pro(p.S164P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000325203
Start	6513718:6513718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1159T>C
AA Mutation	p.Tyr387His(p.Y387H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000325203
Start	6562730:6562730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.205G>A
AA Mutation	p.Ala69Thr(p.A69T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000325203
Start	6562841:6562841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.94A>G
AA Mutation	p.Lys32Glu(p.K32E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000325203
Start	6562868:6562868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142616217
CDS Mutation	c.67C>T
AA Mutation	p.Arg23Trp(p.R23W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000325203
Start	6527652:6527652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.469G>A
AA Mutation	p.Glu157Lys(p.E157K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000325203
Start	6562666:6562666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.269A>G
AA Mutation	p.Asn90Ser(p.N90S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000325203
Start	6521284:6521284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.693A>T
AA Mutation	p.Glu231Asp(p.E231D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325203
Start	6519906:6519906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.888C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325203
Start	6521374:6521374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.603G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325203
Start	6513794:6513794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200777464
CDS Mutation	c.1083G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325203
Start	6519981:6519981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.813C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325203
Start	6521263:6521263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs55633437
CDS Mutation	c.714G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000325203
Start	6514688:6514688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1021G>T
AA Mutation	p.Glu341Ter(p.E341*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000325203
Start	6527677:6527677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.445-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ANGPT2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325203
Start	6514749:6514749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139416191
CDS Mutation	c.960C>G
Mutation Classification	Silent
Feature Type	Transcript