Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CASP10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000272879
Start	201228954:201228954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1437G>T
AA Mutation	p.Lys479Asn(p.K479N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000272879
Start	201205914:201205914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.754G>A
AA Mutation	p.Val252Ile(p.V252I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000272879
Start	201228980:201228980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1463G>T
AA Mutation	p.Arg488Ile(p.R488I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000272879
Start	201208164:201208164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.903A>C
AA Mutation	p.Gln301His(p.Q301H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000272879
Start	201185972:201185972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.195C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000272879
Start	201195912:201195912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.648C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000272879
Start	201209131:201209131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.984G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000272879
Start	201209333:201209334(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1189_1190delTT
AA Mutation	p.Phe397HisfsTer7(p.F397Hfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000272879
Start	201209319:201209319(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1176delA
AA Mutation	p.Lys392AsnfsTer26(p.K392Nfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CASP10

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000272879
Start	201209131:201209131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.984G>A
Mutation Classification	Silent
Feature Type	Transcript