Mutation

Primary Site >> Stomach Cancer

Gene >> AMY2A

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000414303
Start	103623936:103623936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1172C>A
AA Mutation	p.Thr391Asn(p.T391N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000414303
Start	103623896:103623896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1132A>G
AA Mutation	p.Asn378Asp(p.N378D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000414303
Start	103617981:103617981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749935390
CDS Mutation	c.196A>G
AA Mutation	p.Ile66Val(p.I66V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000414303
Start	103619714:103619714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.674T>G
AA Mutation	p.Ile225Ser(p.I225S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000414303
Start	103617601:103617601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148925092
CDS Mutation	c.161G>A
AA Mutation	p.Gly54Glu(p.G54E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000414303
Start	103620605:103620605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760571073
CDS Mutation	c.799C>T
AA Mutation	p.Arg267Trp(p.R267W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000414303
Start	103623881:103623881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1117G>A
AA Mutation	p.Val373Ile(p.V373I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000414303
Start	103619604:103619604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.564T>G
AA Mutation	p.Asp188Glu(p.D188E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000414303
Start	103617450:103617450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.10T>A
AA Mutation	p.Phe4Ile(p.F4I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000414303
Start	103618051:103618051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.266G>C
AA Mutation	p.Gly89Ala(p.G89A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000414303
Start	103623923:103623923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1159A>G
AA Mutation	p.Ile387Val(p.I387V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000414303
Start	103617608:103617608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.168G>T
AA Mutation	p.Gln56His(p.Q56H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000414303
Start	103620560:103620560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.754C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000414303
Start	103617512:103617512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.72A>G
Mutation Classification	Silent
Feature Type	Transcript