Colon Cancer: Gene >> SLC25A23

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301454
Start	6454397:6454397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.721C>A
AA Mutation	p.Leu241Met(p.L241M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000301454
Start	6454681:6454681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753656506
CDS Mutation	c.520G>A
AA Mutation	p.Glu174Lys(p.E174K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000301454
Start	6458209:6458209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs549386407
CDS Mutation	c.272G>A
AA Mutation	p.Arg91Gln(p.R91Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000301454
Start	6452364:6452364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1019C>A
AA Mutation	p.Pro340His(p.P340H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000301454
Start	6452320:6452320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748515868
CDS Mutation	c.1063G>A
AA Mutation	p.Val355Ile(p.V355I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000301454
Start	6442088:6442088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs563978358
CDS Mutation	c.1294C>T
AA Mutation	p.Arg432Trp(p.R432W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000301454
Start	6454360:6454360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.758C>T
AA Mutation	p.Ala253Val(p.A253V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000301454
Start	6452353:6452353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1030G>A
AA Mutation	p.Gly344Ser(p.G344S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301454
Start	6452420:6452420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140701489
CDS Mutation	c.963C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301454
Start	6456447:6456447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149525556
CDS Mutation	c.456C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301454
Start	6452321:6452321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1062C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301454
Start	6454035:6454035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.849C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000301454
Start	6442088:6442088(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1294delC
AA Mutation	p.Arg432GlyfsTer12(p.R432Gfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000301454
Start	6457564:6457564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.310C>T
AA Mutation	p.Gln104Ter(p.Q104*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SLC25A23

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301454
Start	6457517:6457517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.357G>A
Mutation Classification	Silent
Feature Type	Transcript