Colon Cancer: Gene >> HDAC11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295757
Start	13502891:13502891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.560G>T
AA Mutation	p.Gly187Val(p.G187V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295757
Start	13481311:13481311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.68G>A
AA Mutation	p.Arg23His(p.R23H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295757
Start	13504658:13504658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1019C>T
AA Mutation	p.Pro340Leu(p.P340L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000295757
Start	13502926:13502926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.595T>C
AA Mutation	p.Tyr199His(p.Y199H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295757
Start	13481342:13481342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.99G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295757
Start	13496774:13496774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.291C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000295757
Start	13498515:13498515(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.375delG
AA Mutation	p.Lys126SerfsTer154(p.K126Sfs*154)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295757
Start	13496768:13496768(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.291delC
AA Mutation	p.Val98LeufsTer14(p.V98Lfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> HDAC11

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295757
Start	13500768:13500768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140627816
CDS Mutation	c.468G>A
Mutation Classification	Silent
Feature Type	Transcript