Colon Cancer: Gene >> SLC30A6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282587
Start	32220691:32220691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1364G>T
AA Mutation	p.Arg455Ile(p.R455I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000282587
Start	32197707:32197707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.546C>A
AA Mutation	p.Ser182Arg(p.S182R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282587
Start	32220221:32220221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.894A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000282587
Start	32171305:32171305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142115336
CDS Mutation	c.22C>T
AA Mutation	p.Arg8Ter(p.R8*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000282587
Start	32220237:32220237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.910C>T
AA Mutation	p.Arg304Ter(p.R304*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SLC30A6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282587
Start	32197751:32197751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755069292
CDS Mutation	c.590G>A
AA Mutation	p.Arg197Gln(p.R197Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282587
Start	32193940:32193940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774435058
CDS Mutation	c.453G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000282587
Start	32220237:32220237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.910C>T
AA Mutation	p.Arg304Ter(p.R304*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript