Colon Cancer: Gene >> SLC22A8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336232
Start	63014811:63014811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.148C>T
AA Mutation	p.Arg50Cys(p.R50C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336232
Start	63014814:63014814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.145T>C
AA Mutation	p.Cys49Arg(p.C49R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000336232
Start	62994662:62994662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1096G>A
AA Mutation	p.Asp366Asn(p.D366N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000336232
Start	62995732:62995732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.973C>T
AA Mutation	p.Arg325Cys(p.R325C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000336232
Start	62993556:62993556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1397C>T
AA Mutation	p.Thr466Met(p.T466M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000336232
Start	63014631:63014631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.328A>G
AA Mutation	p.Thr110Ala(p.T110A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336232
Start	63014806:63014806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs4149180
CDS Mutation	c.153G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000336232
Start	63014662:63014662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.297G>A
AA Mutation	p.Trp99Ter(p.W99*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SLC22A8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336232
Start	62999013:62999013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780773317
CDS Mutation	c.669C>A
AA Mutation	p.Phe223Leu(p.F223L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript