Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> NTN4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000343702
Start	95787349:95787349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762617558
CDS Mutation	c.175G>A
AA Mutation	p.Glu59Lys(p.E59K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000343702
Start	95787415:95787415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748149271
CDS Mutation	c.109C>T
AA Mutation	p.Arg37Trp(p.R37W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000343702
Start	95683711:95683711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1181C>T
AA Mutation	p.Pro394Leu(p.P394L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000343702
Start	95787286:95787286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.238T>C
AA Mutation	p.Cys80Arg(p.C80R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000343702
Start	95683537:95683537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1355C>T
AA Mutation	p.Ala452Val(p.A452V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000343702
Start	95683707:95683707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1185T>G
AA Mutation	p.Cys395Trp(p.C395W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000343702
Start	95659135:95659135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1838C>A
AA Mutation	p.Pro613His(p.P613H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000343702
Start	95787198:95787198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778122235
CDS Mutation	c.326C>T
AA Mutation	p.Ala109Val(p.A109V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000343702
Start	95659099:95659099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1874G>T
AA Mutation	p.Arg625Ile(p.R625I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343702
Start	95713222:95713222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374055562
CDS Mutation	c.981C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343702
Start	95670139:95670139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750900283
CDS Mutation	c.1518C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000343702
Start	95683607:95683607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1285C>T
AA Mutation	p.Arg429Ter(p.R429*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000343702
Start	95738115:95738115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.615C>A
AA Mutation	p.Tyr205Ter(p.Y205*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NTN4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000343702
Start	95787349:95787349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762617558
CDS Mutation	c.175G>A
AA Mutation	p.Glu59Lys(p.E59K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000343702
Start	95683707:95683707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1185T>G
AA Mutation	p.Cys395Trp(p.C395W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000343702
Start	95665932:95665932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1628A>G
AA Mutation	p.Glu543Gly(p.E543G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000343702
Start	95659130:95659130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1843C>T
AA Mutation	p.Leu615Phe(p.L615F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343702
Start	95710592:95710592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759165554
CDS Mutation	c.1029C>T
Mutation Classification	Silent
Feature Type	Transcript