Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> NME9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000333911
Start	138318192:138318192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200732318
CDS Mutation	c.223G>A
AA Mutation	p.Glu75Lys(p.E75K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000333911
Start	138303638:138303638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.797G>A
AA Mutation	p.Arg266Gln(p.R266Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000333911
Start	138305008:138305008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764706723
CDS Mutation	c.656T>C
AA Mutation	p.Val219Ala(p.V219A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000333911
Start	138304922:138304922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763521362
CDS Mutation	c.742G>A
AA Mutation	p.Val248Ile(p.V248I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000333911
Start	138306477:138306477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.464C>T
AA Mutation	p.Ser155Leu(p.S155L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333911
Start	138306458:138306458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.483C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NME9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000333911
Start	138318192:138318192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200732318
CDS Mutation	c.223G>A
AA Mutation	p.Glu75Lys(p.E75K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000333911
Start	138303638:138303638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.797G>A
AA Mutation	p.Arg266Gln(p.R266Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000333911
Start	138303602:138303602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.833T>C
AA Mutation	p.Val278Ala(p.V278A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript