Colon Cancer: Gene >> TPPP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360578
Start	666107:666107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.328A>C
AA Mutation	p.Thr110Pro(p.T110P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360578
Start	677912:677912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.149C>T
AA Mutation	p.Ala50Val(p.A50V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360578
Start	665222:665222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.540C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360578
Start	677785:677785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs190532828
CDS Mutation	c.276C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360578
Start	677806:677806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.255G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360578
Start	666041:666045(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.390_394delCAAGA
AA Mutation	p.Asp130GlufsTer162(p.D130Efs*162)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TPPP

No Mutation Annotation!