Colon Cancer: Gene >> PDLIM7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355841
Start	177483961:177483961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs550156356
CDS Mutation	c.1193C>T
AA Mutation	p.Thr398Met(p.T398M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355841
Start	177491895:177491895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.310T>A
AA Mutation	p.Tyr104Asn(p.Y104N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355841
Start	177491076:177491076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.469C>T
AA Mutation	p.Pro157Ser(p.P157S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000355841
Start	177496455:177496455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.58G>T
AA Mutation	p.Gly20Trp(p.G20W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000355841
Start	177488144:177488144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.974G>T
AA Mutation	p.Gly325Val(p.G325V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000355841
Start	177496463:177496463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.50G>A
AA Mutation	p.Arg17Gln(p.R17Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000355841
Start	177484072:177484072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs535394998
CDS Mutation	c.1169G>A
AA Mutation	p.Arg390Gln(p.R390Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355841
Start	177483960:177483960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775765511
CDS Mutation	c.1194G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355841
Start	177488209:177488209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.909G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355841
Start	177492420:177492420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.264G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355841
Start	177483876:177483876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143980931
CDS Mutation	c.1278C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PDLIM7

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355841
Start	177483960:177483960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775765511
CDS Mutation	c.1194G>A
Mutation Classification	Silent
Feature Type	Transcript