Colon Cancer: Gene >> PTGDS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371625
Start	136977604:136977604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.26T>C
AA Mutation	p.Met9Thr(p.M9T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371625
Start	136977641:136977641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.63G>T
AA Mutation	p.Gln21His(p.Q21H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371625
Start	136980002:136980002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.388C>A
AA Mutation	p.Leu130Met(p.L130M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371625
Start	136979998:136979998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373555075
CDS Mutation	c.384C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PTGDS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371625
Start	136980234:136980234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.500G>A
AA Mutation	p.Cys167Tyr(p.C167Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript