Colon Cancer: Gene >> SLC52A3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000217254
Start	765744:765744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746808726
CDS Mutation	c.31G>A
AA Mutation	p.Val11Ile(p.V11I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000217254
Start	765249:765249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781769616
CDS Mutation	c.526G>A
AA Mutation	p.Val176Ile(p.V176I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000217254
Start	765213:765213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752459961
CDS Mutation	c.562G>A
AA Mutation	p.Ala188Thr(p.A188T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000217254
Start	765575:765575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.200G>A
AA Mutation	p.Ser67Asn(p.S67N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000217254
Start	761135:761135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752924421
CDS Mutation	c.1301C>T
AA Mutation	p.Ala434Val(p.A434V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217254
Start	763677:763677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532778217
CDS Mutation	c.894G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217254
Start	763737:763737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756359704
CDS Mutation	c.834G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217254
Start	765214:765214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs546271483
CDS Mutation	c.561C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217254
Start	765739:765739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777780132
CDS Mutation	c.36C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SLC52A3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000217254
Start	763643:763643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145194879
CDS Mutation	c.928G>A
AA Mutation	p.Val310Ile(p.V310I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217254
Start	763791:763791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.780C>T
Mutation Classification	Silent
Feature Type	Transcript