Colon Cancer: Gene >> PALLD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000505667
Start	168511958:168511958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.454G>A
AA Mutation	p.Val152Ile(p.V152I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000505667
Start	168903893:168903893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2609C>A
AA Mutation	p.Ala870Asp(p.A870D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000505667
Start	168511643:168511643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.139C>T
AA Mutation	p.Arg47Trp(p.R47W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000505667
Start	168690693:168690693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs535947672
CDS Mutation	c.1426C>T
AA Mutation	p.Arg476Trp(p.R476W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000505667
Start	168894622:168894622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2144C>T
AA Mutation	p.Ala715Val(p.A715V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000505667
Start	168511531:168511531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.27C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000505667
Start	168512365:168512365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.861A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000505667
Start	168512239:168512239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.735C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000505667
Start	168512140:168512140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.636A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000505667
Start	168898657:168898657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2415C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PALLD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000505667
Start	168913948:168913948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758884211
CDS Mutation	c.2644C>T
AA Mutation	p.Arg882Trp(p.R882W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000505667
Start	168925058:168925058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3338C>T
AA Mutation	p.Thr1113Ile(p.T1113I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000505667
Start	168925061:168925061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3341C>T
AA Mutation	p.Ala1114Val(p.A1114V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000505667
Start	168711851:168711851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1892A>C
AA Mutation	p.Lys631Thr(p.K631T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000505667
Start	168891022:168891022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2065C>T
AA Mutation	p.Arg689Cys(p.R689C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000505667
Start	168511843:168511843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.339C>A
Mutation Classification	Silent
Feature Type	Transcript