Mutation

Primary Site >> Stomach Cancer

Gene >> DTL

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366991
Start	212101064:212101064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369056190
CDS Mutation	c.2074G>A
AA Mutation	p.Gly692Arg(p.G692R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366991
Start	212064994:212064994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.604A>G
AA Mutation	p.Lys202Glu(p.K202E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000366991
Start	212100645:212100645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1655A>G
AA Mutation	p.Lys552Arg(p.K552R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000366991
Start	212047174:212047174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756969574
CDS Mutation	c.301G>A
AA Mutation	p.Val101Ile(p.V101I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000366991
Start	212100855:212100855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs550425709
CDS Mutation	c.1865C>T
AA Mutation	p.Pro622Leu(p.P622L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000366991
Start	212100570:212100570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768119065
CDS Mutation	c.1580C>T
AA Mutation	p.Pro527Leu(p.P527L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366991
Start	212064951:212064951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.561A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366991
Start	212080695:212080695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1206A>G
Mutation Classification	Silent
Feature Type	Transcript