Colon Cancer: Gene >> KRT19

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361566
Start	41523824:41523824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1122G>T
AA Mutation	p.Glu374Asp(p.E374D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361566
Start	41524848:41524848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.655G>A
AA Mutation	p.Glu219Lys(p.E219K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361566
Start	41528070:41528070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.178G>T
AA Mutation	p.Ala60Ser(p.A60S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361566
Start	41524894:41524894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.609G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361566
Start	41528068:41528068(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.180delC
AA Mutation	p.Tyr61ThrfsTer9(p.Y61Tfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> KRT19

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361566
Start	41527893:41527893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.355C>A
AA Mutation	p.Gln119Lys(p.Q119K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript