Colon Cancer: Gene >> PDGFA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354513
Start	501164:501164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145010817
CDS Mutation	c.532G>A
AA Mutation	p.Ala178Thr(p.A178T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354513
Start	510900:510900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.362C>T
AA Mutation	p.Pro121Leu(p.P121L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000354513
Start	510831:510831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs184796222
CDS Mutation	c.431G>A
AA Mutation	p.Arg144His(p.R144H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000354513
Start	518977:518977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.25C>T
AA Mutation	p.Leu9Phe(p.L9F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000354513
Start	510919:510919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775727803
CDS Mutation	c.343G>A
AA Mutation	p.Ala115Thr(p.A115T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000354513
Start	500466:500466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs570502707
CDS Mutation	c.614G>T
AA Mutation	p.Arg205Ile(p.R205I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354513
Start	510893:510893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771182613
CDS Mutation	c.369C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000354513
Start	501200:501200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.496G>T
AA Mutation	p.Glu166Ter(p.E166*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PDGFA

No Mutation Annotation!