Mutation

Primary Site >> Stomach Cancer

Gene >> CCR3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357422
Start	46266083:46266083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202200691
CDS Mutation	c.925C>T
AA Mutation	p.Arg309Trp(p.R309W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357422
Start	46265817:46265817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.659C>A
AA Mutation	p.Thr220Lys(p.T220K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000357422
Start	46266096:46266096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201751920
CDS Mutation	c.938G>A
AA Mutation	p.Arg313His(p.R313H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000357422
Start	46265620:46265620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.462C>A
AA Mutation	p.Ser154Arg(p.S154R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000357422
Start	46265625:46265625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.467T>G
AA Mutation	p.Val156Gly(p.V156G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000357422
Start	46265627:46265627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.469A>C
AA Mutation	p.Thr157Pro(p.T157P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000357422
Start	46265981:46265981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs41276535
CDS Mutation	c.823C>T
AA Mutation	p.Arg275Trp(p.R275W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000357422
Start	46265516:46265516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.358G>C
AA Mutation	p.Glu120Gln(p.E120Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000357422
Start	46265895:46265895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756281359
CDS Mutation	c.737C>T
AA Mutation	p.Ala246Val(p.A246V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000357422
Start	46265213:46265213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.55G>A
AA Mutation	p.Asp19Asn(p.D19N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357422
Start	46265464:46265464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.306C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357422
Start	46266151:46266151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.993T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357422
Start	46265485:46265485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.327C>A
Mutation Classification	Silent
Feature Type	Transcript