Colon Cancer: Gene >> SLC39A6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000269187
Start	36109613:36109613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778520944
CDS Mutation	c.2248G>A
AA Mutation	p.Val750Met(p.V750M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000269187
Start	36123544:36123544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1091T>G
AA Mutation	p.Leu364Arg(p.L364R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000269187
Start	36114260:36114260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1680C>A
AA Mutation	p.Asp560Glu(p.D560E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000269187
Start	36114199:36114199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1741C>T
AA Mutation	p.Arg581Cys(p.R581C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000269187
Start	36109607:36109607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201226313
CDS Mutation	c.2254C>T
AA Mutation	p.Arg752Cys(p.R752C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269187
Start	36114164:36114164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749682154
CDS Mutation	c.1776C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269187
Start	36124584:36124584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.906T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269187
Start	36114293:36114293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1647C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000269187
Start	36126284:36126284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.724G>T
AA Mutation	p.Glu242Ter(p.E242*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000269187
Start	36114391:36114392(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1548_1549insATGGTA
AA Mutation	p.Glu516_Val517insMetVal(p.E516_V517insMV)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SLC39A6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000269187
Start	36124651:36124651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.839T>G
AA Mutation	p.Val280Gly(p.V280G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269187
Start	36114113:36114113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1827C>T
Mutation Classification	Silent
Feature Type	Transcript