Colon Cancer: Gene >> ARID5A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357485
Start	96551804:96551804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1276G>A
AA Mutation	p.Ala426Thr(p.A426T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357485
Start	96551362:96551362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.834G>C
AA Mutation	p.Glu278Asp(p.E278D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000357485
Start	96551376:96551376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.848G>T
AA Mutation	p.Gly283Val(p.G283V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000357485
Start	96549429:96549429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753830076
CDS Mutation	c.229G>A
AA Mutation	p.Glu77Lys(p.E77K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000357485
Start	96551861:96551861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773876068
CDS Mutation	c.1333C>T
AA Mutation	p.Arg445Cys(p.R445C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000357485
Start	96551910:96551910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1382C>T
AA Mutation	p.Ala461Val(p.A461V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357485
Start	96549338:96549338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs563247696
CDS Mutation	c.138C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000357485
Start	96551159:96551159(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.636delC
AA Mutation	p.Arg213GlyfsTer55(p.R213Gfs*55)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ARID5A

Mutation ID	1
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000357485
Start	96550683:96550683(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.523delG
AA Mutation	p.Ala175ProfsTer17(p.A175Pfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript