Colon Cancer: Gene >> PIP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000291009
Start	143139590:143139590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.389T>A
AA Mutation	p.Ile130Asn(p.I130N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000291009
Start	143139581:143139581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780595639
CDS Mutation	c.380C>A
AA Mutation	p.Ala127Asp(p.A127D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000291009
Start	143132180:143132180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.64C>A
AA Mutation	p.Gln22Lys(p.Q22K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000291009
Start	143132190:143132190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.74C>T
AA Mutation	p.Ala25Val(p.A25V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000291009
Start	143139537:143139537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367785031
CDS Mutation	c.336C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000291009
Start	143135221:143135221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.123C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PIP

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000291009
Start	143135195:143135195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376369577
CDS Mutation	c.97C>T
AA Mutation	p.Arg33Trp(p.R33W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000291009
Start	143135279:143135279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.181G>T
AA Mutation	p.Glu61Ter(p.E61*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript