Colon Cancer: Gene >> SLC25A5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317881
Start	119469988:119469988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.439A>G
AA Mutation	p.Lys147Glu(p.K147E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000317881
Start	119468606:119468606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.91C>T
AA Mutation	p.Arg31Trp(p.R31W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000317881
Start	119470922:119470922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs796575701
CDS Mutation	c.761C>T
AA Mutation	p.Thr254Met(p.T254M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000317881
Start	119470477:119470477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.703C>T
AA Mutation	p.Arg235Cys(p.R235C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000317881
Start	119469866:119469866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.317G>T
AA Mutation	p.Arg106Ile(p.R106I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000317881
Start	119469837:119469837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.288G>T
AA Mutation	p.Lys96Asn(p.K96N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317881
Start	119470410:119470410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.636C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000317881
Start	119471041:119471042(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.880_881insAATCC
AA Mutation	p.Ile294LysfsTer28(p.I294Kfs*28)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000317881
Start	119469957:119469962(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.409_414delGCCCGT
AA Mutation	p.Ala137_Arg138del(p.A137_R138del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SLC25A5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317881
Start	119470477:119470477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.703C>T
AA Mutation	p.Arg235Cys(p.R235C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript