Colon Cancer: Gene >> TMPRSS13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000524993
Start	117904057:117904057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773942328
CDS Mutation	c.1426G>A
AA Mutation	p.Asp476Asn(p.D476N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000524993
Start	117904095:117904095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777748954
CDS Mutation	c.1388C>T
AA Mutation	p.Thr463Ile(p.T463I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000524993
Start	117918730:117918730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761322256
CDS Mutation	c.130G>A
AA Mutation	p.Ala44Thr(p.A44T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000524993
Start	117908662:117908662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1232A>G
AA Mutation	p.Asp411Gly(p.D411G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000524993
Start	117908653:117908653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1241A>G
AA Mutation	p.Asp414Gly(p.D414G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000524993
Start	117918541:117918541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.319G>A
AA Mutation	p.Ala107Thr(p.A107T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000524993
Start	117929294:117929294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.14G>A
AA Mutation	p.Ser5Asn(p.S5N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000524993
Start	117904049:117904049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1434G>T
AA Mutation	p.Lys478Asn(p.K478N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000524993
Start	117914474:117914474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs535811734
CDS Mutation	c.597G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000524993
Start	117909925:117909925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781418596
CDS Mutation	c.990G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TMPRSS13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000524993
Start	117908648:117908648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1246G>A
AA Mutation	p.Ala416Thr(p.A416T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000524993
Start	117908700:117908700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745923344
CDS Mutation	c.1194C>T
Mutation Classification	Silent
Feature Type	Transcript