Colon Cancer: Gene >> SLC2A5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377424
Start	9057585:9057585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.156G>T
AA Mutation	p.Glu52Asp(p.E52D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377424
Start	9039566:9039566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.982A>G
AA Mutation	p.Met328Val(p.M328V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377424
Start	9041845:9041845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.511A>G
AA Mutation	p.Thr171Ala(p.T171A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377424
Start	9039808:9039808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.877G>A
AA Mutation	p.Val293Ile(p.V293I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377424
Start	9038881:9038881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1045T>C
AA Mutation	p.Phe349Leu(p.F349L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000377424
Start	9047690:9047690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368743770
CDS Mutation	c.338C>T
AA Mutation	p.Ala113Val(p.A113V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000377424
Start	9057538:9057538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761342863
CDS Mutation	c.203C>T
AA Mutation	p.Thr68Met(p.T68M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377424
Start	9040107:9040107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.654G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377424
Start	9038849:9038849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1077C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377424
Start	9039971:9039971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766297608
CDS Mutation	c.714C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377424
Start	9040164:9040164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.597C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377424
Start	9039896:9039896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.789C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377424
Start	9037952:9037952(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1247delG
AA Mutation	p.Gly416AlafsTer13(p.G416Afs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SLC2A5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377424
Start	9037661:9037661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1431G>T
AA Mutation	p.Lys477Asn(p.K477N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377424
Start	9040143:9040143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.618G>A
Mutation Classification	Silent
Feature Type	Transcript