Colon Cancer: Gene >> SLC25A6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381401
Start	1391974:1391974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.36C>A
AA Mutation	p.Phe12Leu(p.F12L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381401
Start	1386706:1386706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.793G>A
AA Mutation	p.Glu265Lys(p.E265K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381401
Start	1389299:1389299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147304014
CDS Mutation	c.540C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381401
Start	1387352:1387352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.666C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381401
Start	1387343:1387343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774859439
CDS Mutation	c.675C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381401
Start	1389704:1389704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201788965
CDS Mutation	c.135C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000381401
Start	1386648:1386648(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.851delG
AA Mutation	p.Gly284AlafsTer14(p.G284Afs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SLC25A6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381401
Start	1389474:1389474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.365C>T
AA Mutation	p.Ala122Val(p.A122V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381401
Start	1391955:1391955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.55G>C
AA Mutation	p.Ala19Pro(p.A19P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript