Colon Cancer: Gene >> PTDSS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000517309
Start	96333486:96333486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1342G>T
AA Mutation	p.Gly448Cys(p.G448C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000517309
Start	96309610:96309610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1061G>A
AA Mutation	p.Cys354Tyr(p.C354Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000517309
Start	96262081:96262081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.41A>G
AA Mutation	p.Asp14Gly(p.D14G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000517309
Start	96287099:96287099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.394T>C
AA Mutation	p.Trp132Arg(p.W132R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000517309
Start	96299770:96299770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.677A>G
AA Mutation	p.Asn226Ser(p.N226S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000517309
Start	96284118:96284118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.281C>G
AA Mutation	p.Thr94Ser(p.T94S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000517309
Start	96295214:96295214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs185374340
CDS Mutation	c.558C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000517309
Start	96309566:96309566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745991363
CDS Mutation	c.1017C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PTDSS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000517309
Start	96320292:96320292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1120G>A
AA Mutation	p.Asp374Asn(p.D374N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000517309
Start	96304132:96304132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.845C>A
AA Mutation	p.Ser282Tyr(p.S282Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000517309
Start	96304113:96304113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142695191
CDS Mutation	c.826C>T
AA Mutation	p.Arg276Ter(p.R276*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript