Mutation

Primary Site >> Stomach Cancer

Gene >> CES1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361503
Start	55828917:55828917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.107A>C
AA Mutation	p.Lys36Thr(p.K36T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361503
Start	55823625:55823625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.461G>T
AA Mutation	p.Gly154Val(p.G154V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361503
Start	55828900:55828900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.124G>A
AA Mutation	p.Gly42Arg(p.G42R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361503
Start	55821393:55821393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.665C>T
AA Mutation	p.Ala222Val(p.A222V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361503
Start	55820425:55820425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778524104
CDS Mutation	c.745G>A
AA Mutation	p.Val249Met(p.V249M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361503
Start	55810529:55810529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376976316
CDS Mutation	c.1303C>T
AA Mutation	p.Arg435Trp(p.R435W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361503
Start	55810528:55810528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145088728
CDS Mutation	c.1304G>A
AA Mutation	p.Arg435Gln(p.R435Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000361503
Start	55816946:55816946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.920A>T
AA Mutation	p.Asp307Val(p.D307V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000361503
Start	55821463:55821463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs563293177
CDS Mutation	c.595C>T
AA Mutation	p.Arg199Cys(p.R199C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000361503
Start	55828882:55828882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.142G>A
AA Mutation	p.Ala48Thr(p.A48T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361503
Start	55823669:55823669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.417C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361503
Start	55819567:55819567(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.871delG
AA Mutation	p.Glu291LysfsTer9(p.E291Kfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript