Colon Cancer: Gene >> SLC2A3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000075120
Start	7929815:7929815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.730G>T
AA Mutation	p.Asp244Tyr(p.D244Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000075120
Start	7930493:7930493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.660G>T
AA Mutation	p.Glu220Asp(p.E220D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000075120
Start	7925936:7925936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.874T>C
AA Mutation	p.Ser292Pro(p.S292P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000075120
Start	7921445:7921445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780023625
CDS Mutation	c.1459G>A
AA Mutation	p.Glu487Lys(p.E487K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000075120
Start	7922826:7922826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201737691
CDS Mutation	c.1267G>A
AA Mutation	p.Ala423Thr(p.A423T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000075120
Start	7931340:7931340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.415C>T
AA Mutation	p.Pro139Ser(p.P139S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000075120
Start	7925882:7925882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149866146
CDS Mutation	c.928G>A
AA Mutation	p.Gly310Ser(p.G310S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000075120
Start	7922922:7922922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1171G>A
AA Mutation	p.Glu391Lys(p.E391K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000075120
Start	7924423:7924423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1055C>T
AA Mutation	p.Ser352Phe(p.S352F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000075120
Start	7930493:7930493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756443597
CDS Mutation	c.660G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000075120
Start	7931341:7931341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773784727
CDS Mutation	c.414G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000075120
Start	7933035:7933035(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.221delG
AA Mutation	p.Gly74ValfsTer2(p.G74Vfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000075120
Start	7923025:7923025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1069-1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> SLC2A3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000075120
Start	7922826:7922826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201737691
CDS Mutation	c.1267G>A
AA Mutation	p.Ala423Thr(p.A423T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000075120
Start	7930598:7930598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762586293
CDS Mutation	c.555G>A
Mutation Classification	Silent
Feature Type	Transcript