Colon Cancer: Gene >> SLC20A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000342228
Start	42444669:42444669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.707C>T
AA Mutation	p.Pro236Leu(p.P236L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000342228
Start	42439623:42439623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138816265
CDS Mutation	c.761G>A
AA Mutation	p.Arg254Gln(p.R254Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000342228
Start	42437298:42437298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1214C>T
AA Mutation	p.Ala405Val(p.A405V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000342228
Start	42459967:42459967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140059610
CDS Mutation	c.542G>A
AA Mutation	p.Arg181Gln(p.R181Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000342228
Start	42437010:42437010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1502C>T
AA Mutation	p.Ala501Val(p.A501V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000342228
Start	42437077:42437077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1435G>T
AA Mutation	p.Asp479Tyr(p.D479Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000342228
Start	42417960:42417960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs387906652
CDS Mutation	c.1802C>T
AA Mutation	p.Ser601Leu(p.S601L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342228
Start	42428797:42428797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1755C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342228
Start	42437573:42437573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.939A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000342228
Start	42444689:42444689(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.687delT
AA Mutation	p.Phe229LeufsTer14(p.F229Lfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SLC20A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000342228
Start	42437002:42437002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1510G>A
AA Mutation	p.Gly504Ser(p.G504S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000342228
Start	42465854:42465854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.353T>A
AA Mutation	p.Ile118Asn(p.I118N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342228
Start	42437258:42437258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs115234947
CDS Mutation	c.1254C>T
Mutation Classification	Silent
Feature Type	Transcript