Mutation

Primary Site >> Stomach Cancer

Gene >> PLEKHA5

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299275
Start	19265833:19265833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.694C>T
AA Mutation	p.Arg232Cys(p.R232C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000299275
Start	19369750:19369750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774894158
CDS Mutation	c.3314C>T
AA Mutation	p.Pro1105Leu(p.P1105L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000299275
Start	19274599:19274599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.911T>C
AA Mutation	p.Ile304Thr(p.I304T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000299275
Start	19255160:19255160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.427G>T
AA Mutation	p.Gly143Cys(p.G143C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000299275
Start	19265834:19265834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.695G>A
AA Mutation	p.Arg232His(p.R232H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000299275
Start	19274710:19274710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1022T>A
AA Mutation	p.Ile341Asn(p.I341N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000299275
Start	19348402:19348402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2404C>T
AA Mutation	p.Pro802Ser(p.P802S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000299275
Start	19283389:19283389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1405C>T
AA Mutation	p.Pro469Ser(p.P469S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000299275
Start	19348452:19348452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2454A>C
AA Mutation	p.Glu818Asp(p.E818D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000299275
Start	19274803:19274803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs569717972
CDS Mutation	c.1115G>A
AA Mutation	p.Ser372Asn(p.S372N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299275
Start	19283436:19283436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1452A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299275
Start	19336556:19336556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201219138
CDS Mutation	c.2181C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299275
Start	19283508:19283508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1524G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299275
Start	19274858:19274858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1170T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000299275
Start	19361584:19361584(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs759995048
CDS Mutation	c.2995delA
AA Mutation	p.Thr999LeufsTer17(p.T999Lfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000299275
Start	19257447:19257447(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.453delA
AA Mutation	p.Val152PhefsTer33(p.V152Ffs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000299275
Start	19369776:19369777(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3340_3341delAT
AA Mutation	p.Met1114ValfsTer10(p.M1114Vfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000299275
Start	19274641:19274641(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.959delA
AA Mutation	p.Lys320ArgfsTer3(p.K320Rfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000299275
Start	19322322:19322322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1921C>T
AA Mutation	p.Arg641Ter(p.R641*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000299275
Start	19274610:19274611(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.929dupA
AA Mutation	p.Asn310LysfsTer8(p.N310Kfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000299275
Start	19257446:19257447(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.453dupA
AA Mutation	p.Val152SerfsTer3(p.V152Sfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	22
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000299275
Start	19345841:19345841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2354-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript