Colon Cancer: Gene >> SLC36A4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326402
Start	93184516:93184516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.184G>T
AA Mutation	p.Val62Leu(p.V62L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000326402
Start	93154128:93154128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1187C>T
AA Mutation	p.Ser396Phe(p.S396F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000326402
Start	93154242:93154242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1073G>A
AA Mutation	p.Gly358Asp(p.G358D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000326402
Start	93165988:93165988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.797T>A
AA Mutation	p.Ile266Lys(p.I266K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000326402
Start	93154131:93154131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1184G>T
AA Mutation	p.Arg395Ile(p.R395I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326402
Start	93148663:93148663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1389C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000326402
Start	93148694:93148694(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1358delA
AA Mutation	p.Asn453IlefsTer4(p.N453Ifs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SLC36A4

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326402
Start	93148798:93148798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267603248
CDS Mutation	c.1254C>T
Mutation Classification	Silent
Feature Type	Transcript