Colon Cancer: Gene >> SLC19A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311124
Start	45525921:45525921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1189G>A
AA Mutation	p.Ala397Thr(p.A397T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311124
Start	45531778:45531778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.560A>C
AA Mutation	p.Tyr187Ser(p.Y187S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311124
Start	45531935:45531935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.403G>A
AA Mutation	p.Ala135Thr(p.A135T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000311124
Start	45531494:45531494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.844T>C
AA Mutation	p.Tyr282His(p.Y282H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000311124
Start	45532103:45532103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.235G>A
AA Mutation	p.Val79Met(p.V79M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000311124
Start	45531988:45531988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.350C>T
AA Mutation	p.Ala117Val(p.A117V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000311124
Start	45531500:45531500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.838G>A
AA Mutation	p.Gly280Ser(p.G280S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000311124
Start	45531724:45531724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.614G>A
AA Mutation	p.Arg205His(p.R205H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000311124
Start	45531902:45531902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771242705
CDS Mutation	c.436C>T
AA Mutation	p.Pro146Ser(p.P146S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000311124
Start	45530883:45530883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1038G>T
AA Mutation	p.Gln346His(p.Q346H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000311124
Start	45515767:45515767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1667C>T
AA Mutation	p.Pro556Leu(p.P556L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000311124
Start	45531433:45531433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772342183
CDS Mutation	c.905C>T
AA Mutation	p.Ala302Val(p.A302V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000311124
Start	45531617:45531617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.721G>T
AA Mutation	p.Ala241Ser(p.A241S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311124
Start	45531840:45531840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148243729
CDS Mutation	c.498C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SLC19A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311124
Start	45531550:45531550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765709900
CDS Mutation	c.788G>A
AA Mutation	p.Arg263Gln(p.R263Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript