Colon Cancer: Gene >> SLC25A24

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000565488
Start	108200083:108200083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.56A>G
AA Mutation	p.Glu19Gly(p.E19G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000565488
Start	108136789:108136789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149670605
CDS Mutation	c.1298G>A
AA Mutation	p.Arg433Gln(p.R433Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000565488
Start	108200064:108200064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.75G>T
AA Mutation	p.Glu25Asp(p.E25D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000565488
Start	108139072:108139072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781747926
CDS Mutation	c.1235G>A
AA Mutation	p.Arg412His(p.R412H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000565488
Start	108148337:108148337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.872G>T
AA Mutation	p.Arg291Ile(p.R291I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000565488
Start	108157561:108157561(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs763273320
CDS Mutation	c.570delA
AA Mutation	p.Lys190AsnfsTer29(p.K190Nfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000565488
Start	108139056:108139056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1249+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000565488
Start	108161180:108161180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.510+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> SLC25A24

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000565488
Start	108148381:108148381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.828G>T
AA Mutation	p.Lys276Asn(p.K276N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000565488
Start	108155002:108155002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.803A>C
AA Mutation	p.Lys268Thr(p.K268T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript