Colon Cancer: Gene >> PELI3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000320740
Start	66473389:66473389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.605G>A
AA Mutation	p.Arg202His(p.R202H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000320740
Start	66475919:66475919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769753649
CDS Mutation	c.1162C>T
AA Mutation	p.Arg388Cys(p.R388C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000320740
Start	66468902:66468902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.222C>A
AA Mutation	p.Ser74Arg(p.S74R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000320740
Start	66475667:66475667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778577702
CDS Mutation	c.910C>T
AA Mutation	p.Arg304Cys(p.R304C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000320740
Start	66471336:66471336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756980058
CDS Mutation	c.319G>A
AA Mutation	p.Val107Ile(p.V107I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000320740
Start	66471277:66471277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.260G>A
AA Mutation	p.Arg87His(p.R87H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000320740
Start	66473800:66473800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.715C>A
AA Mutation	p.Leu239Met(p.L239M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000320740
Start	66473287:66473287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747361415
CDS Mutation	c.503C>T
AA Mutation	p.Thr168Met(p.T168M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000320740
Start	66471328:66471328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.311A>C
AA Mutation	p.Lys104Thr(p.K104T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000320740
Start	66471321:66471321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.304G>A
AA Mutation	p.Gly102Arg(p.G102R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320740
Start	66476131:66476131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1374C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320740
Start	66475849:66475849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765127805
CDS Mutation	c.1092C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000320740
Start	66473740:66473740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.655C>T
AA Mutation	p.Arg219Ter(p.R219*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PELI3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000320740
Start	66473283:66473283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.499G>T
AA Mutation	p.Asp167Tyr(p.D167Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript