Colon Cancer: Gene >> ACE2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000252519
Start	15570309:15570309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1882C>T
AA Mutation	p.Leu628Phe(p.L628F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000252519
Start	15571636:15571636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747988885
CDS Mutation	c.1825G>A
AA Mutation	p.Asp609Asn(p.D609N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000252519
Start	15581320:15581320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.971C>G
AA Mutation	p.Thr324Ser(p.T324S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000252519
Start	15581281:15581281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1010G>A
AA Mutation	p.Gly337Glu(p.G337E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000252519
Start	15564064:15564064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2269A>G
AA Mutation	p.Ile757Val(p.I757V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000252519
Start	15571624:15571624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1837T>C
AA Mutation	p.Tyr613His(p.Y613H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000252519
Start	15573427:15573427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1481A>G
AA Mutation	p.Asp494Gly(p.D494G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000252519
Start	15578295:15578295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1091T>C
AA Mutation	p.Val364Ala(p.V364A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000252519
Start	15570317:15570317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1874A>C
AA Mutation	p.Lys625Thr(p.K625T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252519
Start	15578285:15578285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750477605
CDS Mutation	c.1101C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252519
Start	15591780:15591780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781175759
CDS Mutation	c.516C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252519
Start	15564149:15564149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2184G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000252519
Start	15573368:15573368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1540C>T
AA Mutation	p.Arg514Ter(p.R514*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ACE2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000252519
Start	15578206:15578206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1180A>C
AA Mutation	p.Asn394His(p.N394H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000252519
Start	15591790:15591790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.506G>T
AA Mutation	p.Arg169Ile(p.R169I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000252519
Start	15566318:15566318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773848804
CDS Mutation	c.2049C>A
AA Mutation	p.Phe683Leu(p.F683L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript