Colon Cancer: Gene >> CPT1A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265641
Start	68757706:68757706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2260C>A
AA Mutation	p.Leu754Met(p.L754M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265641
Start	68784924:68784924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376844032
CDS Mutation	c.1054C>T
AA Mutation	p.Arg352Trp(p.R352W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265641
Start	68781805:68781805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1318G>A
AA Mutation	p.Ala440Thr(p.A440T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265641
Start	68781879:68781879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs528019785
CDS Mutation	c.1244C>T
AA Mutation	p.Ala415Val(p.A415V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265641
Start	68812569:68812569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.149T>C
AA Mutation	p.Ile50Thr(p.I50T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265641
Start	68794904:68794904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.779T>G
AA Mutation	p.Leu260Arg(p.L260R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265641
Start	68804025:68804025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.530C>A
AA Mutation	p.Pro177Gln(p.P177Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265641
Start	68761573:68761573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1990T>A
AA Mutation	p.Ser664Thr(p.S664T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000265641
Start	68781817:68781817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1306A>G
AA Mutation	p.Met436Val(p.M436V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000265641
Start	68784852:68784852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755556780
CDS Mutation	c.1126G>A
AA Mutation	p.Gly376Arg(p.G376R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000265641
Start	68773375:68773375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1630G>A
AA Mutation	p.Val544Met(p.V544M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265641
Start	68799344:68799344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.567G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265641
Start	68781953:68781953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1170C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265641
Start	68773352:68773352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1653C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000265641
Start	68761689:68761689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1876-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CPT1A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265641
Start	68807598:68807598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762094475
CDS Mutation	c.322G>A
AA Mutation	p.Val108Met(p.V108M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265641
Start	68775414:68775414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1477A>G
AA Mutation	p.Ser493Gly(p.S493G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265641
Start	68759624:68759624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2180T>C
AA Mutation	p.Val727Ala(p.V727A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265641
Start	68799288:68799288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.623A>C
AA Mutation	p.Asp208Ala(p.D208A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265641
Start	68775415:68775415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1476C>T
Mutation Classification	Silent
Feature Type	Transcript