Mutation

Primary Site >> Stomach Cancer

Gene >> FARP1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000319562
Start	98438814:98438814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768787362
CDS Mutation	c.2285G>A
AA Mutation	p.Arg762His(p.R762H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000319562
Start	98440759:98440759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765939276
CDS Mutation	c.2719C>T
AA Mutation	p.Arg907Cys(p.R907C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000319562
Start	98431174:98431174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2037C>A
AA Mutation	p.Asn679Lys(p.N679K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000319562
Start	98439971:98439971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2444G>T
AA Mutation	p.Ser815Ile(p.S815I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000319562
Start	98377888:98377888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200784439
CDS Mutation	c.466G>A
AA Mutation	p.Ala156Thr(p.A156T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000319562
Start	98384787:98384787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.554A>G
AA Mutation	p.Tyr185Cys(p.Y185C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000319562
Start	98439135:98439135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766670787
CDS Mutation	c.2372G>A
AA Mutation	p.Arg791Gln(p.R791Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000319562
Start	98446197:98446197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2896T>A
AA Mutation	p.Ser966Thr(p.S966T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000319562
Start	98440730:98440730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2690G>A
AA Mutation	p.Arg897His(p.R897H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000319562
Start	98368125:98368125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747102282
CDS Mutation	c.328C>T
AA Mutation	p.His110Tyr(p.H110Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000319562
Start	98440760:98440760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753430729
CDS Mutation	c.2720G>A
AA Mutation	p.Arg907His(p.R907H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319562
Start	98440198:98440198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2592C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319562
Start	98395385:98395385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1323C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319562
Start	98448284:98448284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757505772
CDS Mutation	c.3105C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319562
Start	98409516:98409516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs560567728
CDS Mutation	c.1593C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319562
Start	98435595:98435595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200427694
CDS Mutation	c.2163G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319562
Start	98368127:98368127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374266525
CDS Mutation	c.330C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319562
Start	98395451:98395451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1389A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319562
Start	98440728:98440728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368496686
CDS Mutation	c.2688G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000319562
Start	98439983:98439983(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2461delG
AA Mutation	p.Val821CysfsTer5(p.V821Cfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000319562
Start	98395458:98395458(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1400delC
AA Mutation	p.Pro467ArgfsTer8(p.P467Rfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000319562
Start	98440222:98440222(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2621delC
AA Mutation	p.Pro874LeufsTer20(p.P874Lfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000319562
Start	98439999:98439999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2472C>A
AA Mutation	p.Cys824Ter(p.C824*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript