Colon Cancer: Gene >> NPSR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360581
Start	34827430:34827430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766192701
CDS Mutation	c.508G>A
AA Mutation	p.Ala170Thr(p.A170T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360581
Start	34848528:34848528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.890A>G
AA Mutation	p.Asp297Gly(p.D297G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359791
Start	34878089:34878089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370072027
CDS Mutation	c.1039C>T
AA Mutation	p.Arg347Cys(p.R347C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360581
Start	34658419:34658419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766121315
CDS Mutation	c.7G>A
AA Mutation	p.Ala3Thr(p.A3T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360581
Start	34827545:34827545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.623C>T
AA Mutation	p.Thr208Ile(p.T208I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000359791
Start	34878133:34878133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1083G>T
AA Mutation	p.Glu361Asp(p.E361D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000360581
Start	34658459:34658459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.47G>A
AA Mutation	p.Gly16Glu(p.G16E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360581
Start	34658502:34658502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.90G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360581
Start	34827438:34827438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.516C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360581
Start	34684585:34684586(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.186dupT
AA Mutation	p.Thr63TyrfsTer45(p.T63Yfs*45)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NPSR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360581
Start	34778465:34778465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs565312186
CDS Mutation	c.284C>A
AA Mutation	p.Ser95Tyr(p.S95Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360581
Start	34834407:34834407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs116249859
CDS Mutation	c.704G>A
AA Mutation	p.Arg235Gln(p.R235Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360581
Start	34684634:34684634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.230G>T
AA Mutation	p.Arg77Ile(p.R77I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript