Colon Cancer: Gene >> KRT77

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341809
Start	52702968:52702968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.467A>T
AA Mutation	p.Glu156Val(p.E156V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341809
Start	52692472:52692472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1376T>C
AA Mutation	p.Leu459Pro(p.L459P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341809
Start	52697804:52697804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764165439
CDS Mutation	c.636G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341809
Start	52703057:52703057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.378C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341809
Start	52702904:52702904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.531C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341809
Start	52703102:52703102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.333T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000341809
Start	52697893:52697893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774353164
CDS Mutation	c.547C>T
AA Mutation	p.Arg183Ter(p.R183*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000341809
Start	52697680:52697680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.758+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> KRT77

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341809
Start	52697843:52697843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.597G>A
Mutation Classification	Silent
Feature Type	Transcript