Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PLRG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000499023
Start	154547824:154547824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.146G>A
AA Mutation	p.Arg49His(p.R49H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000499023
Start	154548895:154548895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.50C>T
AA Mutation	p.Ser17Leu(p.S17L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000499023
Start	154537417:154537417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144644967
CDS Mutation	c.1354G>A
AA Mutation	p.Ala452Thr(p.A452T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000499023
Start	154547046:154547046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.278T>G
AA Mutation	p.Phe93Cys(p.F93C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000499023
Start	154544461:154544461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760558300
CDS Mutation	c.578C>T
AA Mutation	p.Pro193Leu(p.P193L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000499023
Start	154547825:154547825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.145C>T
AA Mutation	p.Arg49Cys(p.R49C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000499023
Start	154540639:154540639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759776348
CDS Mutation	c.894G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PLRG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000499023
Start	154536688:154536688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1542T>G
AA Mutation	p.Phe514Leu(p.F514L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000499023
Start	154538076:154538076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1184T>C
AA Mutation	p.Ile395Thr(p.I395T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000499023
Start	154540796:154540796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.826G>A
AA Mutation	p.Glu276Lys(p.E276K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript