Colon Cancer: Gene >> TFDP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000489671
Start	141974166:141974166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.545G>A
AA Mutation	p.Arg182Gln(p.R182Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000489671
Start	141978671:141978671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.368A>C
AA Mutation	p.Lys123Thr(p.K123T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000489671
Start	142005492:142005492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.135G>T
AA Mutation	p.Lys45Asn(p.K45N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000489671
Start	141963818:141963818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.878G>T
AA Mutation	p.Ser293Ile(p.S293I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000489671
Start	141963899:141963899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.797C>T
AA Mutation	p.Pro266Leu(p.P266L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000489671
Start	142005476:142005476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.151T>G
AA Mutation	p.Leu51Val(p.L51V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TFDP2

No Mutation Annotation!