Colon Cancer: Gene >> NTSR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306928
Start	11662110:11662110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.755G>A
AA Mutation	p.Ser252Asn(p.S252N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306928
Start	11662219:11662219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780850319
CDS Mutation	c.646G>A
AA Mutation	p.Val216Met(p.V216M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000306928
Start	11660086:11660086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149468069
CDS Mutation	c.946C>T
AA Mutation	p.Arg316Cys(p.R316C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000306928
Start	11661997:11661997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.868C>T
AA Mutation	p.Arg290Cys(p.R290C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000306928
Start	11660052:11660052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377014236
CDS Mutation	c.980C>T
AA Mutation	p.Ala327Val(p.A327V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000306928
Start	11658717:11658717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200323530
CDS Mutation	c.995T>C
AA Mutation	p.Leu332Pro(p.L332P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306928
Start	11660066:11660066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs554839273
CDS Mutation	c.966C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000306928
Start	11662189:11662194(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.671_676delTCCTGA
AA Mutation	p.Phe224_Asn226delinsTyr(p.F224_N226delinsY)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NTSR2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306928
Start	11658668:11658668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143067546
CDS Mutation	c.1044C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306928
Start	11662052:11662052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.813C>A
Mutation Classification	Silent
Feature Type	Transcript