Colon Cancer: Gene >> TPP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299427
Start	6615551:6615551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1157C>A
AA Mutation	p.Thr386Asn(p.T386N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000299427
Start	6616795:6616795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.752T>G
AA Mutation	p.Phe251Cys(p.F251C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000299427
Start	6617367:6617367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.442A>G
AA Mutation	p.Thr148Ala(p.T148A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000299427
Start	6616771:6616771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140176031
CDS Mutation	c.776G>A
AA Mutation	p.Arg259His(p.R259H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000299427
Start	6616747:6616747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.800G>C
AA Mutation	p.Gly267Ala(p.G267A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000299427
Start	6616813:6616813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754161261
CDS Mutation	c.734G>A
AA Mutation	p.Arg245His(p.R245H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000299427
Start	6616831:6616831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.716A>G
AA Mutation	p.Asp239Gly(p.D239G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000299427
Start	6615256:6615256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs119455956
CDS Mutation	c.1340G>A
AA Mutation	p.Arg447His(p.R447H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299427
Start	6616028:6616028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1122C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299427
Start	6614980:6614980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1437A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299427
Start	6617008:6617008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.654T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000299427
Start	6614968:6614968(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1449delG
AA Mutation	p.Ile484SerfsTer4(p.I484Sfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000299427
Start	6618774:6618774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.229+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TPP1

No Mutation Annotation!