Colon Cancer: Gene >> SLC22A5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000245407
Start	132390718:132390718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1081C>T
AA Mutation	p.Leu361Phe(p.L361F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000245407
Start	132384172:132384172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781721860
CDS Mutation	c.523G>A
AA Mutation	p.Val175Met(p.V175M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000245407
Start	132392577:132392577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs386134223
CDS Mutation	c.1412G>A
AA Mutation	p.Arg471His(p.R471H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000245407
Start	132390722:132390722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1085C>T
AA Mutation	p.Ser362Leu(p.S362L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000245407
Start	132392606:132392606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs11568513
CDS Mutation	c.1441G>A
AA Mutation	p.Val481Ile(p.V481I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000245407
Start	132370115:132370115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.143A>G
AA Mutation	p.His48Arg(p.H48R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000245407
Start	132384219:132384219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs561032476
CDS Mutation	c.570G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000245407
Start	132387039:132387039(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs386134209
CDS Mutation	c.844delC
AA Mutation	p.Arg282AspfsTer14(p.R282Dfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SLC22A5

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000245407
Start	132392605:132392605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150457229
CDS Mutation	c.1440C>T
Mutation Classification	Silent
Feature Type	Transcript