Colon Cancer: Gene >> SLC2A9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264784
Start	9942041:9942041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.686G>T
AA Mutation	p.Ser229Ile(p.S229I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264784
Start	9996883:9996883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.308C>A
AA Mutation	p.Pro103Gln(p.P103Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000264784
Start	9980735:9980735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370374119
CDS Mutation	c.538G>A
AA Mutation	p.Val180Ile(p.V180I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264784
Start	9980680:9980680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756988113
CDS Mutation	c.593G>A
AA Mutation	p.Arg198His(p.R198H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264784
Start	9887618:9887618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1240C>A
AA Mutation	p.Leu414Met(p.L414M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264784
Start	9920483:9920483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.904G>A
AA Mutation	p.Val302Met(p.V302M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264784
Start	10021329:10021329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.101T>G
AA Mutation	p.Leu34Arg(p.L34R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264784
Start	10021283:10021283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.147A>T
AA Mutation	p.Arg49Ser(p.R49S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000264784
Start	9826445:9826445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1575G>T
AA Mutation	p.Glu525Asp(p.E525D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264784
Start	9980697:9980697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.576C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264784
Start	9826439:9826439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1581C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264784
Start	9996840:9996840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148002726
CDS Mutation	c.351C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000264784
Start	9890684:9890684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1141A>T
AA Mutation	p.Arg381Ter(p.R381*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SLC2A9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264784
Start	9834977:9834977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1323C>A
AA Mutation	p.Phe441Leu(p.F441L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264784
Start	9826545:9826545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1475C>T
AA Mutation	p.Ala492Val(p.A492V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264784
Start	10021405:10021405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.25T>C
AA Mutation	p.Ser9Pro(p.S9P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000264784
Start	9908346:9908346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1003-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript