Colon Cancer: Gene >> INO80C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334598
Start	35480551:35480551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.169G>A
AA Mutation	p.Glu57Lys(p.E57K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000334598
Start	35497793:35497793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768152671
CDS Mutation	c.82T>C
AA Mutation	p.Ser28Pro(p.S28P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334598
Start	35479403:35479403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.276C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> INO80C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334598
Start	35468627:35468627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.563C>T
AA Mutation	p.Thr188Met(p.T188M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334598
Start	35479340:35479340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.339T>C
Mutation Classification	Silent
Feature Type	Transcript