Colon Cancer: Gene >> NAPEPLD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341533
Start	103119716:103119716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.802G>T
AA Mutation	p.Gly268Cys(p.G268C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341533
Start	103128709:103128709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.68A>G
AA Mutation	p.Lys23Arg(p.K23R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000341533
Start	103103508:103103508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778037217
CDS Mutation	c.1103A>G
AA Mutation	p.Tyr368Cys(p.Y368C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000341533
Start	103103491:103103491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1120G>T
AA Mutation	p.Asp374Tyr(p.D374Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000341533
Start	103120199:103120199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.319C>T
AA Mutation	p.Leu107Phe(p.L107F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000341533
Start	103120022:103120022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746125875
CDS Mutation	c.496C>T
AA Mutation	p.Arg166Cys(p.R166C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000341533
Start	103119979:103119979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367936558
CDS Mutation	c.539C>T
AA Mutation	p.Ala180Val(p.A180V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341533
Start	103103534:103103534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1077G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341533
Start	103120125:103120125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.393A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341533
Start	103120080:103120080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373616514
CDS Mutation	c.438G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000341533
Start	103119676:103119676(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs746683932
CDS Mutation	c.842delT
AA Mutation	p.Phe281SerfsTer14(p.F281Sfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000341533
Start	103120074:103120075(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.443_444delCC
AA Mutation	p.Pro148HisfsTer3(p.P148Hfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NAPEPLD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341533
Start	103119676:103119676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.842T>C
AA Mutation	p.Phe281Ser(p.F281S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341533
Start	103120022:103120022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746125875
CDS Mutation	c.496C>T
AA Mutation	p.Arg166Cys(p.R166C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000341533
Start	103119628:103119628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762301264
CDS Mutation	c.890G>T
AA Mutation	p.Arg297Ile(p.R297I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript