Colon Cancer: Gene >> KRT13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000246635
Start	41503324:41503324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.698A>C
AA Mutation	p.Asn233Thr(p.N233T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000246635
Start	41502377:41502377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1241C>A
AA Mutation	p.Ala414Asp(p.A414D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000246635
Start	41505141:41505141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138959511
CDS Mutation	c.410G>A
AA Mutation	p.Arg137His(p.R137H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000246635
Start	41501736:41501736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1253G>A
AA Mutation	p.Gly418Asp(p.G418D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000246635
Start	41505163:41505163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.388G>A
AA Mutation	p.Ala130Thr(p.A130T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246635
Start	41503657:41503657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368494222
CDS Mutation	c.564C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246635
Start	41505473:41505473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.78C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246635
Start	41503018:41503018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375082810
CDS Mutation	c.816C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246635
Start	41503335:41503335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779846006
CDS Mutation	c.687C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> KRT13

No Mutation Annotation!