Colon Cancer: Gene >> NT5C1A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000235628
Start	39659293:39659293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.935C>T
AA Mutation	p.Ala312Val(p.A312V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000235628
Start	39659263:39659263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs190344471
CDS Mutation	c.965G>A
AA Mutation	p.Arg322His(p.R322H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000235628
Start	39659426:39659426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.802G>T
AA Mutation	p.Gly268Cys(p.G268C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000235628
Start	39659380:39659380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775212324
CDS Mutation	c.848G>A
AA Mutation	p.Arg283His(p.R283H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000235628
Start	39659363:39659363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200357710
CDS Mutation	c.865G>A
AA Mutation	p.Gly289Arg(p.G289R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000235628
Start	39659221:39659221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1007G>A
AA Mutation	p.Gly336Glu(p.G336E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000235628
Start	39659357:39659357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs539519081
CDS Mutation	c.871C>T
AA Mutation	p.Arg291Trp(p.R291W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000235628
Start	39665590:39665590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751249522
CDS Mutation	c.364G>A
AA Mutation	p.Asp122Asn(p.D122N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000235628
Start	39663427:39663427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.441C>A
AA Mutation	p.Phe147Leu(p.F147L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000235628
Start	39671940:39671940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.99C>A
AA Mutation	p.Phe33Leu(p.F33L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000235628
Start	39671927:39671927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.112G>A
AA Mutation	p.Ala38Thr(p.A38T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000235628
Start	39661121:39661121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.699C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000235628
Start	39663391:39663391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777691580
CDS Mutation	c.477G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000235628
Start	39659480:39659481(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.747dupC
AA Mutation	p.Phe253LeufsTer7(p.F253Lfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NT5C1A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000235628
Start	39665584:39665584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.370G>A
AA Mutation	p.Val124Ile(p.V124I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000235628
Start	39659420:39659420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756357555
CDS Mutation	c.808C>T
AA Mutation	p.Arg270Trp(p.R270W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000235628
Start	39659338:39659338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777598956
CDS Mutation	c.890G>A
AA Mutation	p.Arg297His(p.R297H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript