Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> HAVCR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307851
Start	157106938:157106938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147605860
CDS Mutation	c.83C>T
AA Mutation	p.Ala28Val(p.A28V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307851
Start	157106800:157106800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.221A>G
AA Mutation	p.Asp74Gly(p.D74G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000307851
Start	157106900:157106900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.121A>G
AA Mutation	p.Thr41Ala(p.T41A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307851
Start	157106820:157106820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.201G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307851
Start	157106919:157106919(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.102delC
AA Mutation	p.Tyr35IlefsTer41(p.Y35Ifs*41)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307851
Start	157106745:157106745(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.276delT
AA Mutation	p.Asp92GlufsTer4(p.D92Efs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> HAVCR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307851
Start	157106760:157106760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.261T>G
AA Mutation	p.Asp87Glu(p.D87E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307851
Start	157106894:157106894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.127G>A
AA Mutation	p.Ala43Thr(p.A43T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000307851
Start	157106727:157106727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.294G>T
AA Mutation	p.Glu98Asp(p.E98D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript