Colon Cancer: Gene >> SLC7A5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261622
Start	87833014:87833014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200265403
CDS Mutation	c.1480G>A
AA Mutation	p.Val494Ile(p.V494I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261622
Start	87834540:87834540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747038000
CDS Mutation	c.1342G>A
AA Mutation	p.Ala448Thr(p.A448T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261622
Start	87841127:87841127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.693C>A
AA Mutation	p.Phe231Leu(p.F231L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261622
Start	87836602:87836602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149119495
CDS Mutation	c.1186G>A
AA Mutation	p.Val396Ile(p.V396I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261622
Start	87841081:87841081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780129662
CDS Mutation	c.739T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261622
Start	87851740:87851740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745656437
CDS Mutation	c.648C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261622
Start	87837932:87837932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199932832
CDS Mutation	c.1053C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SLC7A5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261622
Start	87869333:87869333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375232549
CDS Mutation	c.90G>C
AA Mutation	p.Lys30Asn(p.K30N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261622
Start	87836627:87836627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771516158
CDS Mutation	c.1161C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261622
Start	87840458:87840458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.786C>T
Mutation Classification	Silent
Feature Type	Transcript