Colon Cancer: Gene >> SLC19A3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000258403
Start	227699327:227699327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.388G>A
AA Mutation	p.Val130Met(p.V130M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000258403
Start	227702251:227702251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121917882
CDS Mutation	c.68G>T
AA Mutation	p.Gly23Val(p.G23V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000258403
Start	227687557:227687557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1331G>T
AA Mutation	p.Ser444Ile(p.S444I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258403
Start	227699442:227699442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.273C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258403
Start	227698970:227698970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143662945
CDS Mutation	c.745C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258403
Start	227695948:227695948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs573958395
CDS Mutation	c.1113G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258403
Start	227695990:227695990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1071C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258403
Start	227687547:227687547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1341A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000258403
Start	227702244:227702245(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs786205213
CDS Mutation	c.74dupT
AA Mutation	p.Ser26LeufsTer19(p.S26Lfs*19)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SLC19A3

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258403
Start	227688183:227688183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766083018
CDS Mutation	c.1297T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000258403
Start	227698757:227698757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.958G>T
AA Mutation	p.Glu320Ter(p.E320*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript