Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> NDC80

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261597
Start	2578012:2578012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.347C>A
AA Mutation	p.Ser116Tyr(p.S116Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261597
Start	2587867:2587867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.707T>G
AA Mutation	p.Phe236Cys(p.F236C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261597
Start	2585130:2585130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.597A>C
AA Mutation	p.Lys199Asn(p.K199N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261597
Start	2578059:2578059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.394C>A
AA Mutation	p.Leu132Ile(p.L132I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261597
Start	2579001:2579001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.551C>T
AA Mutation	p.Ala184Val(p.A184V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261597
Start	2589232:2589232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.792G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261597
Start	2595456:2595456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1056A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261597
Start	2601453:2601453(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1438delA
AA Mutation	p.Met480TrpfsTer7(p.M480Wfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000261597
Start	2578017:2578017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs542320666
CDS Mutation	c.352C>T
AA Mutation	p.Gln118Ter(p.Q118*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NDC80

No Mutation Annotation!