Colon Cancer: Gene >> HOOK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397668
Start	12772668:12772668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.401G>T
AA Mutation	p.Arg134Ile(p.R134I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000397668
Start	12765830:12765830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1604T>A
AA Mutation	p.Ile535Asn(p.I535N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000397668
Start	12767888:12767888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751125633
CDS Mutation	c.1231C>T
AA Mutation	p.Arg411Trp(p.R411W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000397668
Start	12763759:12763759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1847C>A
AA Mutation	p.Pro616His(p.P616H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000397668
Start	12763338:12763338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371657591
CDS Mutation	c.2104C>T
AA Mutation	p.Arg702Cys(p.R702C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000397668
Start	12773020:12773020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs567279935
CDS Mutation	c.229C>T
AA Mutation	p.Arg77Trp(p.R77W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397668
Start	12767421:12767421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763056963
CDS Mutation	c.1347C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397668
Start	12765042:12765042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1680G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000397668
Start	12767829:12767829(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1290delG
AA Mutation	p.Leu431Ter(p.L431*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000397668
Start	12763736:12763736(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1870delG
AA Mutation	p.Ala624HisfsTer8(p.A624Hfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000397668
Start	12764846:12764846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372675413
CDS Mutation	c.1795C>T
AA Mutation	p.Arg599Ter(p.R599*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000397668
Start	12772651:12772651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.418G>T
AA Mutation	p.Glu140Ter(p.E140*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> HOOK2

No Mutation Annotation!