Colon Cancer: Gene >> SPARC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000231061
Start	151673206:151673206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.131G>A
AA Mutation	p.Gly44Glu(p.G44E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000231061
Start	151664204:151664204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370328004
CDS Mutation	c.766C>T
AA Mutation	p.Arg256Cys(p.R256C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000231061
Start	151664200:151664200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.770C>T
AA Mutation	p.Ala257Val(p.A257V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000231061
Start	151666429:151666429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.666G>T
AA Mutation	p.Lys222Asn(p.K222N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000231061
Start	151667514:151667514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.538G>A
AA Mutation	p.Glu180Lys(p.E180K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000231061
Start	151669702:151669702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.413G>T
AA Mutation	p.Gly138Val(p.G138V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000231061
Start	151676140:151676140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.49G>A
AA Mutation	p.Ala17Thr(p.A17T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000231061
Start	151671642:151671642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.261G>T
AA Mutation	p.Glu87Asp(p.E87D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231061
Start	151664220:151664220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.750C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000231061
Start	151676202:151676202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.-13-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> SPARC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000231061
Start	151671653:151671653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754817963
CDS Mutation	c.250G>A
AA Mutation	p.Glu84Lys(p.E84K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000231061
Start	151666428:151666428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.667A>G
AA Mutation	p.Asn223Asp(p.N223D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000231061
Start	151671584:151671584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.319G>T
AA Mutation	p.Glu107Ter(p.E107*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript