Colon Cancer: Gene >> PDLIM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397760
Start	22581404:22581404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.119A>G
AA Mutation	p.Asp40Gly(p.D40G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397760
Start	22593767:22593767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762318482
CDS Mutation	c.916C>T
AA Mutation	p.Arg306Cys(p.R306C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000397760
Start	22585102:22585102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.401G>T
AA Mutation	p.Ser134Ile(p.S134I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397760
Start	22581456:22581456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755738040
CDS Mutation	c.171G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397760
Start	22593823:22593823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.972G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000397760
Start	22593772:22593772(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.924delC
AA Mutation	p.Gly309AlafsTer10(p.G309Afs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000397760
Start	22585394:22585394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369238305
CDS Mutation	c.535C>T
AA Mutation	p.Arg179Ter(p.R179*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000397760
Start	22580658:22580659(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.59dupG
AA Mutation	p.Arg21GlnfsTer11(p.R21Qfs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PDLIM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397760
Start	22593829:22593829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.978C>G
AA Mutation	p.Phe326Leu(p.F326L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397760
Start	22591638:22591638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.851A>C
AA Mutation	p.His284Pro(p.H284P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000397760
Start	22589682:22589682(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.709delC
AA Mutation	p.Arg237AspfsTer29(p.R237Dfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript