Colon Cancer: Gene >> HSPB8

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281938
Start	119179438:119179438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763658767
CDS Mutation	c.126C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000281938
Start	119179572:119179572(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.266delC
AA Mutation	p.Pro89HisfsTer12(p.P89Hfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000281938
Start	119179571:119179572(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs773017653
CDS Mutation	c.266dupC
AA Mutation	p.Pro90ThrfsTer37(p.P90Tfs*37)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> HSPB8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000281938
Start	119179398:119179398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.86G>A
AA Mutation	p.Arg29His(p.R29H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000281938
Start	119193752:119193752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.485G>A
AA Mutation	p.Gly162Asp(p.G162D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000281938
Start	119187031:119187031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.374A>T
AA Mutation	p.His125Leu(p.H125L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000281938
Start	119179528:119179528(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.219delC
AA Mutation	p.Thr74LeufsTer27(p.T74Lfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript