Colon Cancer: Gene >> SLC30A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367001
Start	211575963:211575963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.949G>T
AA Mutation	p.Asp317Tyr(p.D317Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367001
Start	211578584:211578584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.29G>T
AA Mutation	p.Arg10Leu(p.R10L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367001
Start	211575715:211575715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1197G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367001
Start	211575616:211575616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369229728
CDS Mutation	c.1296G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367001
Start	211578421:211578421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.192C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000367001
Start	211575837:211575837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1075G>T
AA Mutation	p.Glu359Ter(p.E359*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SLC30A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367001
Start	211575978:211575978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.934T>A
AA Mutation	p.Trp312Arg(p.W312R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367001
Start	211575984:211575984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.928C>T
AA Mutation	p.Pro310Ser(p.P310S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367001
Start	211576272:211576273(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.639_640delAA
AA Mutation	p.Ser214TrpfsTer2(p.S214Wfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript