Mutation

Primary Site >> Stomach Cancer

Gene >> ESCO2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000305188
Start	27776778:27776778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.470C>A
AA Mutation	p.Pro157His(p.P157H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000305188
Start	27799547:27799547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767123113
CDS Mutation	c.1504C>T
AA Mutation	p.Arg502Cys(p.R502C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000305188
Start	27792738:27792738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1424A>C
AA Mutation	p.Lys475Thr(p.K475T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000305188
Start	27791979:27791979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768258688
CDS Mutation	c.1280G>A
AA Mutation	p.Arg427His(p.R427H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305188
Start	27803390:27803390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1758C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305188
Start	27776548:27776548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758624389
CDS Mutation	c.240G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305188
Start	27792748:27792748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1434T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305188
Start	27799600:27799600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1557T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305188
Start	27776974:27776974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201608468
CDS Mutation	c.666G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000305188
Start	27776939:27776939(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.636delT
AA Mutation	p.Phe212LeufsTer35(p.F212Lfs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000305188
Start	27776402:27776402(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.98delA
AA Mutation	p.Lys33SerfsTer25(p.K33Sfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000305188
Start	27776432:27776432(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.128delA
AA Mutation	p.Asn43MetfsTer15(p.N43Mfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000305188
Start	27787976:27787976(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1111delA
AA Mutation	p.Thr371GlnfsTer24(p.T371Qfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000305188
Start	27776525:27776525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.217C>T
AA Mutation	p.Gln73Ter(p.Q73*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript