Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> NME7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367811
Start	169298566:169298566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.638C>A
AA Mutation	p.Ser213Tyr(p.S213Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367811
Start	169324437:169324437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755169173
CDS Mutation	c.67C>T
AA Mutation	p.Arg23Cys(p.R23C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367811
Start	169324451:169324451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.53C>T
AA Mutation	p.Ala18Val(p.A18V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367811
Start	169298650:169298650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139755731
CDS Mutation	c.554G>A
AA Mutation	p.Arg185His(p.R185H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000367811
Start	169324440:169324440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781410209
CDS Mutation	c.64C>T
AA Mutation	p.Arg22Ter(p.R22*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NME7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367811
Start	169323121:169323121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.274G>A
AA Mutation	p.Glu92Lys(p.E92K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000367811
Start	169230744:169230744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138530600
CDS Mutation	c.964C>T
AA Mutation	p.Arg322Ter(p.R322*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000367811
Start	169324440:169324440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781410209
CDS Mutation	c.64C>T
AA Mutation	p.Arg22Ter(p.R22*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript