Colon Cancer: Gene >> PDLIM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329399
Start	95263888:95263888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.509G>A
AA Mutation	p.Ser170Asn(p.S170N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000329399
Start	95247306:95247306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.594G>T
AA Mutation	p.Lys198Asn(p.K198N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000329399
Start	95271739:95271739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.142G>T
AA Mutation	p.Asp48Tyr(p.D48Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000329399
Start	95247329:95247329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151177027
CDS Mutation	c.571G>A
AA Mutation	p.Asp191Asn(p.D191N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000329399
Start	95263951:95263951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.446G>A
AA Mutation	p.Gly149Asp(p.G149D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000329399
Start	95263864:95263864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.533C>T
AA Mutation	p.Pro178Leu(p.P178L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000329399
Start	95263967:95263967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.430T>C
AA Mutation	p.Tyr144His(p.Y144H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000329399
Start	95271692:95271692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.189C>A
AA Mutation	p.His63Gln(p.H63Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000329399
Start	95238059:95238059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.856T>C
AA Mutation	p.Cys286Arg(p.C286R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329399
Start	95271746:95271746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.135T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329399
Start	95264007:95264007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764741236
CDS Mutation	c.390G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000329399
Start	95237930:95237931(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.984dupC
AA Mutation	p.Lys329GlnfsTer7(p.K329Qfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PDLIM1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329399
Start	95247270:95247270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141682059
CDS Mutation	c.630G>A
Mutation Classification	Silent
Feature Type	Transcript