Colon Cancer: Gene >> NT5E

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000257770
Start	85485300:85485300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775412849
CDS Mutation	c.817C>T
AA Mutation	p.Arg273Trp(p.R273W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000257770
Start	85490612:85490612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781684532
CDS Mutation	c.1315G>A
AA Mutation	p.Val439Met(p.V439M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000257770
Start	85492087:85492087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143859595
CDS Mutation	c.1471G>A
AA Mutation	p.Glu491Lys(p.E491K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000257770
Start	85485334:85485334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.851G>A
AA Mutation	p.Gly284Asp(p.G284D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000257770
Start	85492083:85492083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1467G>T
AA Mutation	p.Met489Ile(p.M489I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257770
Start	85471385:85471385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778273365
CDS Mutation	c.711C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000257770
Start	85492003:85492003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755218216
CDS Mutation	c.1387C>T
AA Mutation	p.Arg463Ter(p.R463*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000257770
Start	85493977:85493978(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1698_1699insAGATATAT
AA Mutation	p.Ala567ArgfsTer5(p.A567Rfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NT5E

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000257770
Start	85492004:85492004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201008460
CDS Mutation	c.1388G>A
AA Mutation	p.Arg463Gln(p.R463Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257770
Start	85485266:85485266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.783G>A
Mutation Classification	Silent
Feature Type	Transcript