Colon Cancer: Gene >> NAP1L1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000261182
Start	76059799:76059799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.428C>T
AA Mutation	p.Ser143Leu(p.S143L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261182
Start	76050638:76050638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.952G>T
AA Mutation	p.Ala318Ser(p.A318S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261182
Start	76049243:76049243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1097A>G
AA Mutation	p.Glu366Gly(p.E366G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261182
Start	76053785:76053785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.755T>G
AA Mutation	p.Ile252Ser(p.I252S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261182
Start	76060200:76060200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.286T>G
AA Mutation	p.Tyr96Asp(p.Y96D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261182
Start	76053223:76053223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.898T>G
AA Mutation	p.Phe300Val(p.F300V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261182
Start	76053278:76053278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.843A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000261182
Start	76050627:76050628(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.962_963insCAATTATTTCTT
AA Mutation	p.Ala321_Ala322insAsnTyrPhePhe(p.A321_A322insNYFF)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NAP1L1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261182
Start	76067470:76067470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.107G>A
AA Mutation	p.Arg36His(p.R36H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261182
Start	76053286:76053286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.835C>T
AA Mutation	p.His279Tyr(p.H279Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261182
Start	76060256:76060256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.230G>A
AA Mutation	p.Arg77Gln(p.R77Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261182
Start	76056138:76056138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.453G>T
AA Mutation	p.Lys151Asn(p.K151N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript