Colon Cancer: Gene >> HEYL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372852
Start	39627051:39627051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.443G>A
AA Mutation	p.Arg148His(p.R148H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372852
Start	39632708:39632708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368236989
CDS Mutation	c.88G>A
AA Mutation	p.Ala30Thr(p.A30T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372852
Start	39626713:39626713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752690094
CDS Mutation	c.781G>A
AA Mutation	p.Ala261Thr(p.A261T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372852
Start	39627052:39627052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747977443
CDS Mutation	c.442C>T
AA Mutation	p.Arg148Cys(p.R148C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000372852
Start	39626730:39626730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.764C>T
AA Mutation	p.Ala255Val(p.A255V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000372852
Start	39631525:39631525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766168978
CDS Mutation	c.202C>T
AA Mutation	p.Arg68Cys(p.R68C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372852
Start	39627110:39627110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.384C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372852
Start	39627020:39627020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372712511
CDS Mutation	c.474C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HEYL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372852
Start	39632707:39632707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.89C>T
AA Mutation	p.Ala30Val(p.A30V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372852
Start	39626678:39626678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766635894
CDS Mutation	c.816C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000372852
Start	39626776:39626776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769070110
CDS Mutation	c.718C>T
AA Mutation	p.Arg240Ter(p.R240*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript