Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SNX9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392185
Start	157942807:157942807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1757G>T
AA Mutation	p.Arg586Met(p.R586M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392185
Start	157921586:157921586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1005G>A
AA Mutation	p.Met335Ile(p.M335I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392185
Start	157906140:157906140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.633T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392185
Start	157906152:157906152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.645C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392185
Start	157928698:157928698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1284G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392185
Start	157901968:157901969(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.545_546delAG
AA Mutation	p.Glu182ValfsTer3(p.E182Vfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392185
Start	157896900:157896900(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.379delG
AA Mutation	p.Ala127ProfsTer75(p.A127Pfs*75)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SNX9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392185
Start	157906207:157906207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.700A>T
AA Mutation	p.Ile234Phe(p.I234F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392185
Start	157901927:157901927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.502G>A
AA Mutation	p.Asp168Asn(p.D168N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000392185
Start	157896936:157896936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.410A>C
AA Mutation	p.Asn137Thr(p.N137T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000392185
Start	157928619:157928619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1205T>G
AA Mutation	p.Val402Gly(p.V402G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript