Colon Cancer: Gene >> SLC13A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000314669
Start	28489227:28489227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.116C>T
AA Mutation	p.Ala39Val(p.A39V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000314669
Start	28494503:28494503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1299G>T
AA Mutation	p.Lys433Asn(p.K433N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000314669
Start	28491746:28491746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782472673
CDS Mutation	c.772G>A
AA Mutation	p.Gly258Ser(p.G258S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000314669
Start	28490463:28490463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.241G>A
AA Mutation	p.Glu81Lys(p.E81K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000314669
Start	28497162:28497162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1672T>G
AA Mutation	p.Trp558Gly(p.W558G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000314669
Start	28496570:28496570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1591C>A
AA Mutation	p.Leu531Ile(p.L531I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314669
Start	28491781:28491781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.807C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314669
Start	28493631:28493631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.939C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314669
Start	28494485:28494485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1281T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314669
Start	28491745:28491745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs117154964
CDS Mutation	c.771C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314669
Start	28489228:28489228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs181965873
CDS Mutation	c.117G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000314669
Start	28491476:28491477(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.614_615insT
AA Mutation	p.Glu205AspfsTer232(p.E205Dfs*232)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SLC13A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000314669
Start	28490492:28490492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.270C>A
AA Mutation	p.Phe90Leu(p.F90L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000314669
Start	28493580:28493580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.888G>T
AA Mutation	p.Lys296Asn(p.K296N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000314669
Start	28493695:28493695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1003C>A
AA Mutation	p.Leu335Ile(p.L335I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript