Mutation

Primary Site >> Stomach Cancer

Gene >> MPL

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372470
Start	43338603:43338603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.274G>A
AA Mutation	p.Val92Met(p.V92M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000372470
Start	43352302:43352302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1652C>T
AA Mutation	p.Pro551Leu(p.P551L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372470
Start	43352561:43352561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1697G>A
AA Mutation	p.Ser566Asn(p.S566N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372470
Start	43340069:43340069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367877736
CDS Mutation	c.796G>A
AA Mutation	p.Gly266Ser(p.G266S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000372470
Start	43338161:43338161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.142C>A
AA Mutation	p.Leu48Ile(p.L48I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000372470
Start	43338553:43338553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148276667
CDS Mutation	c.224G>A
AA Mutation	p.Arg75His(p.R75H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372470
Start	43339485:43339485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.606A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372470
Start	43340002:43340002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.729C>A
Mutation Classification	Silent
Feature Type	Transcript