Colon Cancer: Gene >> ANXA13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000419625
Start	123695536:123695536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.437G>T
AA Mutation	p.Gly146Val(p.G146V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000419625
Start	123684659:123684659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs112185912
CDS Mutation	c.782C>T
AA Mutation	p.Ala261Val(p.A261V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000419625
Start	123688876:123688876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.713C>G
AA Mutation	p.Thr238Ser(p.T238S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000419625
Start	123698499:123698499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.247C>A
AA Mutation	p.Leu83Ile(p.L83I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000419625
Start	123684633:123684633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.808C>T
AA Mutation	p.Arg270Cys(p.R270C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000419625
Start	123681295:123681295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.896T>G
AA Mutation	p.Val299Gly(p.V299G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000419625
Start	123684640:123684640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369931826
CDS Mutation	c.801G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000419625
Start	123702708:123702708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751181283
CDS Mutation	c.120C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	start_lost
Transcription ID	ENST00000419625
Start	123737333:123737333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2T>C
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ANXA13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000419625
Start	123681338:123681338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.853G>T
AA Mutation	p.Ala285Ser(p.A285S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000419625
Start	123693746:123693746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.505G>T
AA Mutation	p.Asp169Tyr(p.D169Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000419625
Start	123698556:123698556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.190C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000419625
Start	123681360:123681360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.832-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript