Colon Cancer: Gene >> BHLHE22

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000321870
Start	64581520:64581520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.730C>T
AA Mutation	p.Arg244Trp(p.R244W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000321870
Start	64581544:64581544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.754C>T
AA Mutation	p.Arg252Cys(p.R252C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000321870
Start	64581920:64581920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1130G>A
AA Mutation	p.Cys377Tyr(p.C377Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000321870
Start	64581587:64581587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.797G>A
AA Mutation	p.Arg266His(p.R266H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000321870
Start	64580833:64580833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.43G>A
AA Mutation	p.Asp15Asn(p.D15N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000321870
Start	64581567:64581567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.777C>A
AA Mutation	p.Asn259Lys(p.N259K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000321870
Start	64581680:64581680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.890C>T
AA Mutation	p.Ala297Val(p.A297V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321870
Start	64581840:64581840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1050C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321870
Start	64581639:64581639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.849C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> BHLHE22

No Mutation Annotation!