Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PGK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373316
Start	78109908:78109908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141397576
CDS Mutation	c.107A>C
AA Mutation	p.Asn36Thr(p.N36T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373316
Start	78114108:78114108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.365T>C
AA Mutation	p.Leu122Pro(p.L122P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373316
Start	78123240:78123240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.802G>T
AA Mutation	p.Asp268Tyr(p.D268Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373316
Start	78124998:78124998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1061C>T
AA Mutation	p.Ala354Val(p.A354V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373316
Start	78123302:78123302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.864T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PGK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373316
Start	78124886:78124886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.949G>A
AA Mutation	p.Gly317Ser(p.G317S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373316
Start	78125030:78125030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1093A>G
AA Mutation	p.Arg365Gly(p.R365G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373316
Start	78118113:78118113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.584A>G
AA Mutation	p.Asn195Ser(p.N195S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373316
Start	78123249:78123249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.811T>C
AA Mutation	p.Ser271Pro(p.S271P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript