Colon Cancer: Gene >> NTN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000173229
Start	9221232:9221232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1476G>T
AA Mutation	p.Lys492Asn(p.K492N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000173229
Start	9182928:9182928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762421437
CDS Mutation	c.1370C>T
AA Mutation	p.Ala457Val(p.A457V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000173229
Start	9022803:9022803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.430G>C
AA Mutation	p.Val144Leu(p.V144L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000173229
Start	9162893:9162893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1099G>A
AA Mutation	p.Val367Ile(p.V367I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000173229
Start	9239949:9239949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1796G>A
AA Mutation	p.Gly599Asp(p.G599D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000173229
Start	9023256:9023256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs577333476
CDS Mutation	c.883G>A
AA Mutation	p.Val295Met(p.V295M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000173229
Start	9162873:9162873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1079C>T
AA Mutation	p.Ser360Leu(p.S360L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000173229
Start	9179889:9179889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1290G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000173229
Start	9022835:9022835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.462G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000173229
Start	9179868:9179868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1269T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000173229
Start	9022738:9022747(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.367_376delGAGAACTACC
AA Mutation	p.Glu123CysfsTer19(p.E123Cfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NTN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000173229
Start	9182933:9182933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376278603
CDS Mutation	c.1375C>A
AA Mutation	p.Pro459Thr(p.P459T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000173229
Start	9239716:9239716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1563T>C
Mutation Classification	Silent
Feature Type	Transcript