Colon Cancer: Gene >> SLC25A3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000228318
Start	98601267:98601267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.914G>T
AA Mutation	p.Arg305Ile(p.R305I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000228318
Start	98601236:98601236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.883A>C
AA Mutation	p.Lys295Gln(p.K295Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000228318
Start	98598625:98598625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.566G>A
AA Mutation	p.Arg189Gln(p.R189Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000228318
Start	98597983:98597983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.410A>C
AA Mutation	p.Lys137Thr(p.K137T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000228318
Start	98598666:98598666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.607G>A
AA Mutation	p.Ala203Thr(p.A203T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000228318
Start	98594010:98594010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.32C>T
AA Mutation	p.Ala11Val(p.A11V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_retained_variant
Transcription ID	ENST00000228318
Start	98601528:98601528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1089G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228318
Start	98601426:98601426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.987G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228318
Start	98601441:98601441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1002C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000228318
Start	98598698:98598698(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.642delA
AA Mutation	p.Ala215HisfsTer11(p.A215Hfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000228318
Start	98595558:98595558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.282+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> SLC25A3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000228318
Start	98601402:98601402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.963G>T
AA Mutation	p.Met321Ile(p.M321I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript