Colon Cancer: Gene >> SPP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000395080
Start	87977068:87977068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.64G>A
AA Mutation	p.Ala22Thr(p.A22T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000395080
Start	87976945:87976945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758126729
CDS Mutation	c.50T>C
AA Mutation	p.Ile17Thr(p.I17T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000395080
Start	87982535:87982535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.584G>T
AA Mutation	p.Ser195Ile(p.S195I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000395080
Start	87981781:87981781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs79496699
CDS Mutation	c.523C>T
AA Mutation	p.Arg175Cys(p.R175C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000395080
Start	87982773:87982773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.822C>A
AA Mutation	p.His274Gln(p.H274Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000395080
Start	87982838:87982838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.887A>C
AA Mutation	p.Lys296Thr(p.K296T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395080
Start	87981555:87981555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.297C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395080
Start	87976931:87976931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.36C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395080
Start	87982635:87982635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.684T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395080
Start	87981576:87981576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150169219
CDS Mutation	c.318C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SPP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000395080
Start	87981690:87981690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.432A>T
AA Mutation	p.Glu144Asp(p.E144D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript