Colon Cancer: Gene >> CA14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369111
Start	150261605:150261605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781966502
CDS Mutation	c.223G>A
AA Mutation	p.Glu75Lys(p.E75K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369111
Start	150263408:150263408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.830C>A
AA Mutation	p.Ser277Tyr(p.S277Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369111
Start	150262163:150262164(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.268_269delCT
AA Mutation	p.Leu90AlafsTer38(p.L90Afs*38)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369111
Start	150262256:150262256(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.360delG
AA Mutation	p.Ser121GlnfsTer27(p.S121Qfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CA14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369111
Start	150262543:150262543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.418G>A
AA Mutation	p.Asp140Asn(p.D140N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369111
Start	150258137:150258137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.9C>T
Mutation Classification	Silent
Feature Type	Transcript