Mutation

Primary Site >> Stomach Cancer

Gene >> FPR1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304748
Start	51746237:51746237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.758G>A
AA Mutation	p.Cys253Tyr(p.C253Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000304748
Start	51746043:51746043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201404212
CDS Mutation	c.952G>A
AA Mutation	p.Ala318Thr(p.A318T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000304748
Start	51746274:51746274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147646924
CDS Mutation	c.721C>T
AA Mutation	p.Arg241Trp(p.R241W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000304748
Start	51746256:51746256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764370052
CDS Mutation	c.739G>A
AA Mutation	p.Ala247Thr(p.A247T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000304748
Start	51746396:51746396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.599T>C
AA Mutation	p.Val200Ala(p.V200A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000304748
Start	51746580:51746580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.415G>A
AA Mutation	p.Val139Met(p.V139M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304748
Start	51746257:51746257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148898220
CDS Mutation	c.738C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304748
Start	51746851:51746851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.144C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000304748
Start	51746820:51746821(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.173_174dupCA
AA Mutation	p.Val59GlnfsTer8(p.V59Qfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript