Colon Cancer: Gene >> GPD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301149
Start	50106874:50106874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.569T>C
AA Mutation	p.Val190Ala(p.V190A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000301149
Start	50107643:50107643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755956209
CDS Mutation	c.689T>C
AA Mutation	p.Leu230Pro(p.L230P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000301149
Start	50107669:50107669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147931328
CDS Mutation	c.715G>A
AA Mutation	p.Ala239Thr(p.A239T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000301149
Start	50105671:50105671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.343G>T
AA Mutation	p.Gly115Cys(p.G115C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301149
Start	50109477:50109477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1008T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301149
Start	50104673:50104673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.141C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000301149
Start	50106287:50106287(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.364delG
AA Mutation	p.Val122Ter(p.X122_splice)
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> GPD1

No Mutation Annotation!