Colon Cancer: Gene >> CD47

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361309
Start	108059500:108059500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.643A>T
AA Mutation	p.Thr215Ser(p.T215S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361309
Start	108049644:108049644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.942A>C
AA Mutation	p.Lys314Asn(p.K314N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361309
Start	108080320:108080320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.71A>C
AA Mutation	p.Lys24Thr(p.K24T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361309
Start	108071124:108071124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.459A>G
AA Mutation	p.Ile153Met(p.I153M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361309
Start	108050591:108050591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.921G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361309
Start	108080010:108080010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777288181
CDS Mutation	c.381C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CD47

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361309
Start	108071105:108071105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.478T>C
AA Mutation	p.Phe160Leu(p.F160L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript