Colon Cancer: Gene >> PDLIM5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317968
Start	94523845:94523845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.218G>A
AA Mutation	p.Cys73Tyr(p.C73Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000317968
Start	94618072:94618072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.989T>C
AA Mutation	p.Leu330Pro(p.L330P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000317968
Start	94575859:94575859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.535C>A
AA Mutation	p.Leu179Met(p.L179M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000317968
Start	94654476:94654476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1300G>A
AA Mutation	p.Ala434Thr(p.A434T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000317968
Start	94585590:94585590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201891054
CDS Mutation	c.736C>T
AA Mutation	p.Arg246Cys(p.R246C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000317968
Start	94640414:94640414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1247G>A
AA Mutation	p.Arg416Gln(p.R416Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000317968
Start	94575818:94575818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.494C>T
AA Mutation	p.Pro165Leu(p.P165L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000317968
Start	94618086:94618086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1003T>G
AA Mutation	p.Ser335Ala(p.S335A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000317968
Start	94523827:94523827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.200A>C
AA Mutation	p.Gln67Pro(p.Q67P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317968
Start	94657483:94657483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766549570
CDS Mutation	c.1521C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317968
Start	94640310:94640310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1143T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317968
Start	94585610:94585610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.756T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PDLIM5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317968
Start	94640414:94640414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1247G>A
AA Mutation	p.Arg416Gln(p.R416Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000317968
Start	94575845:94575845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.521T>C
AA Mutation	p.Phe174Ser(p.F174S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000317968
Start	94618193:94618193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1108+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript