Colon Cancer: Gene >> SLC22A17

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000206544
Start	23346749:23346749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1516C>T
AA Mutation	p.Arg506Trp(p.R506W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000206544
Start	23347723:23347723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.953C>T
AA Mutation	p.Ala318Val(p.A318V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000206544
Start	23347720:23347720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.956A>G
AA Mutation	p.His319Arg(p.H319R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000206544
Start	23352024:23352024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.191C>T
AA Mutation	p.Pro64Leu(p.P64L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000206544
Start	23352192:23352192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.23C>T
AA Mutation	p.Thr8Met(p.T8M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000206544
Start	23347918:23347918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.917A>C
AA Mutation	p.Lys306Thr(p.K306T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000206544
Start	23347524:23347524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1152C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000206544
Start	23352041:23352041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.174G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000206544
Start	23347692:23347692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.984G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000206544
Start	23348215:23348215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.784C>T
AA Mutation	p.Arg262Ter(p.R262*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SLC22A17

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000206544
Start	23347568:23347568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1108C>A
AA Mutation	p.Leu370Ile(p.L370I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000206544
Start	23347602:23347602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1074C>T
Mutation Classification	Silent
Feature Type	Transcript