Colon Cancer: Gene >> MANEA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358812
Start	95586493:95586493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.54T>G
AA Mutation	p.Phe18Leu(p.F18L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358812
Start	95586503:95586503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.64C>A
AA Mutation	p.Leu22Met(p.L22M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358812
Start	95606316:95606316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1300C>A
AA Mutation	p.Leu434Ile(p.L434I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358812
Start	95586967:95586967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.528G>A
AA Mutation	p.Met176Ile(p.M176I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000358812
Start	95596846:95596846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.654G>T
AA Mutation	p.Lys218Asn(p.K218N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000358812
Start	95605912:95605912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.896T>G
AA Mutation	p.Phe299Cys(p.F299C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000358812
Start	95586518:95586518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.79A>C
AA Mutation	p.Lys27Gln(p.K27Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000358812
Start	95596811:95596811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.619A>G
AA Mutation	p.Thr207Ala(p.T207A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MANEA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358812
Start	95605840:95605840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.824C>A
AA Mutation	p.Pro275His(p.P275H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript