Colon Cancer: Gene >> NTSR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370501
Start	62709475:62709475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.268C>T
AA Mutation	p.Arg90Trp(p.R90W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370501
Start	62709703:62709703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.496C>T
AA Mutation	p.Arg166Cys(p.R166C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370501
Start	62760157:62760157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1147T>C
AA Mutation	p.Cys383Arg(p.C383R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370501
Start	62709520:62709520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.313C>A
AA Mutation	p.Leu105Met(p.L105M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370501
Start	62760251:62760251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766991609
CDS Mutation	c.1241G>A
AA Mutation	p.Arg414His(p.R414H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000370501
Start	62709649:62709649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764154462
CDS Mutation	c.442C>T
AA Mutation	p.Arg148Cys(p.R148C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000370501
Start	62760173:62760173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148516370
CDS Mutation	c.1163G>A
AA Mutation	p.Arg388His(p.R388H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370501
Start	62709633:62709633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.426C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370501
Start	62754870:62754870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772417399
CDS Mutation	c.900C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370501
Start	62760081:62760081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1071C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370501
Start	62709852:62709852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369573865
CDS Mutation	c.645C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370501
Start	62709372:62709372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.165C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370501
Start	62709802:62709802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147663707
CDS Mutation	c.595C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370501
Start	62709881:62709881(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.678delC
AA Mutation	p.Thr227ProfsTer29(p.T227Pfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NTSR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370501
Start	62709458:62709458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766108856
CDS Mutation	c.251C>T
AA Mutation	p.Thr84Met(p.T84M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370501
Start	62709616:62709616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.409G>A
AA Mutation	p.Gly137Ser(p.G137S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370501
Start	62709655:62709655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753717597
CDS Mutation	c.448G>A
AA Mutation	p.Ala150Thr(p.A150T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370501
Start	62758322:62758322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766656202
CDS Mutation	c.973A>G
AA Mutation	p.Met325Val(p.M325V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370501
Start	62709402:62709402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.195G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370501
Start	62709807:62709807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776251796
CDS Mutation	c.600G>A
Mutation Classification	Silent
Feature Type	Transcript