Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PLS3

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000355899
Start	115645099:115645099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370999829
CDS Mutation	c.1262C>T
AA Mutation	p.Ala421Val(p.A421V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000355899
Start	115647894:115647894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1637A>G
AA Mutation	p.Asp546Gly(p.D546G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355899
Start	115629259:115629259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.299A>C
AA Mutation	p.Lys100Thr(p.K100T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000355899
Start	115634061:115634061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.562C>A
AA Mutation	p.Leu188Ile(p.L188I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355899
Start	115643474:115643474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1149A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000355899
Start	115629306:115629306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.346G>T
AA Mutation	p.Gly116Ter(p.G116*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000355899
Start	115629863:115629863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.396G>A
AA Mutation	p.Trp132Ter(p.W132*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000355899
Start	115629261:115629261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.301G>T
AA Mutation	p.Glu101Ter(p.E101*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PLS3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355899
Start	115647561:115647561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1523A>G
AA Mutation	p.Asn508Ser(p.N508S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355899
Start	115640465:115640465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.949G>A
AA Mutation	p.Gly317Ser(p.G317S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355899
Start	115643380:115643380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1055T>G
AA Mutation	p.Phe352Cys(p.F352C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355899
Start	115646162:115646162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782148043
CDS Mutation	c.1353G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355899
Start	115640443:115640443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.927C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000355899
Start	115629879:115629879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.412G>T
AA Mutation	p.Glu138Ter(p.E138*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript