Colon Cancer: Gene >> SLC22A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366953
Start	160256652:160256652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.480C>A
AA Mutation	p.Phe160Leu(p.F160L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366953
Start	160247277:160247277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.864G>T
AA Mutation	p.Arg288Ser(p.R288S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000366953
Start	160243742:160243742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1109G>T
AA Mutation	p.Gly370Val(p.G370V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000366953
Start	160249301:160249301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.757G>A
AA Mutation	p.Ala253Thr(p.A253T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000366953
Start	160243644:160243644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1207C>G
AA Mutation	p.Arg403Gly(p.R403G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000366953
Start	160243730:160243730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1121A>G
AA Mutation	p.Asp374Gly(p.D374G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000366953
Start	160249367:160249367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371586429
CDS Mutation	c.691C>T
AA Mutation	p.Arg231Trp(p.R231W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366953
Start	160243576:160243576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1275T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000366953
Start	160242385:160242385(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1297delA
AA Mutation	p.Ile433LeufsTer17(p.I433Lfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SLC22A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366953
Start	160247232:160247232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.909T>G
AA Mutation	p.Ile303Met(p.I303M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366953
Start	160242385:160242385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1297A>C
AA Mutation	p.Ile433Leu(p.I433L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript