Colon Cancer: Gene >> CASP5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260315
Start	105008900:105008900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748713070
CDS Mutation	c.88G>A
AA Mutation	p.Val30Met(p.V30M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000260315
Start	105003288:105003288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.529A>C
AA Mutation	p.Lys177Gln(p.K177Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000260315
Start	105000353:105000353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.860T>G
AA Mutation	p.Leu287Arg(p.L287R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000260315
Start	104997481:104997481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1108T>C
AA Mutation	p.Trp370Arg(p.W370R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000260315
Start	105007143:105007143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.373G>A
AA Mutation	p.Ala125Thr(p.A125T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000260315
Start	105007245:105007245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs543265797
CDS Mutation	c.271G>A
AA Mutation	p.Asp91Asn(p.D91N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000260315
Start	105008951:105008951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.37A>C
AA Mutation	p.Asn13His(p.N13H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260315
Start	104998967:104998967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1014G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000260315
Start	105003284:105003284(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.533delA
AA Mutation	p.Asn178IlefsTer8(p.N178Ifs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000260315
Start	105002185:105002185(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.560delA
AA Mutation	p.Lys187ArgfsTer33(p.K187Rfs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000260315
Start	105003309:105003309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.508G>T
AA Mutation	p.Glu170Ter(p.E170*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000260315
Start	104998884:104998884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141481245
CDS Mutation	c.1096+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CASP5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260315
Start	105002048:105002048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747113465
CDS Mutation	c.697G>A
AA Mutation	p.Glu233Lys(p.E233K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000260315
Start	105000296:105000296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.917A>T
AA Mutation	p.Lys306Ile(p.K306I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000260315
Start	104998905:104998905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1076C>A
AA Mutation	p.Ala359Asp(p.A359D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript