Colon Cancer: Gene >> SLC5A7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264047
Start	107997891:107997891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.502T>C
AA Mutation	p.Ser168Pro(p.S168P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264047
Start	107992999:107992999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.320G>A
AA Mutation	p.Arg107His(p.R107H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264047
Start	108008548:108008548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.979C>A
AA Mutation	p.Leu327Ile(p.L327I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264047
Start	108010709:108010709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1591C>A
AA Mutation	p.Leu531Ile(p.L531I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264047
Start	107988183:107988183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.28G>A
AA Mutation	p.Ala10Thr(p.A10T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264047
Start	108010796:108010796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770906251
CDS Mutation	c.1678A>G
AA Mutation	p.Lys560Glu(p.K560E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264047
Start	108010369:108010369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1251C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264047
Start	108010249:108010249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267598829
CDS Mutation	c.1131C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264047
Start	108001944:108001944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.645C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SLC5A7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264047
Start	107992982:107992982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.303C>A
AA Mutation	p.Phe101Leu(p.F101L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264047
Start	108008571:108008571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1002C>A
AA Mutation	p.Phe334Leu(p.F334L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264047
Start	108010391:108010391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1273C>T
AA Mutation	p.Leu425Phe(p.L425F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264047
Start	108006144:108006144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369809428
CDS Mutation	c.837C>T
Mutation Classification	Silent
Feature Type	Transcript