Mutation

Primary Site >> Stomach Cancer

Gene >> PHLDB2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000393925
Start	111885369:111885369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759923986
CDS Mutation	c.1292G>A
AA Mutation	p.Arg431Gln(p.R431Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000393925
Start	111885341:111885341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1264C>T
AA Mutation	p.Arg422Cys(p.R422C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000393925
Start	111974429:111974429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3628A>G
AA Mutation	p.Asn1210Asp(p.N1210D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000393925
Start	111884979:111884979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.902A>G
AA Mutation	p.Tyr301Cys(p.Y301C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000393925
Start	111952642:111952642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371213542
CDS Mutation	c.2702G>A
AA Mutation	p.Arg901Gln(p.R901Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000393925
Start	111974490:111974490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3689C>T
AA Mutation	p.Ser1230Leu(p.S1230L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000393925
Start	111884520:111884520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772453408
CDS Mutation	c.443A>G
AA Mutation	p.Tyr148Cys(p.Y148C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000393925
Start	111973771:111973771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3575A>G
AA Mutation	p.Gln1192Arg(p.Q1192R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000393925
Start	111913490:111913490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1507G>A
AA Mutation	p.Asp503Asn(p.D503N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000393925
Start	111913671:111913671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1688G>A
AA Mutation	p.Ser563Asn(p.S563N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000393925
Start	111884459:111884459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.382T>A
AA Mutation	p.Phe128Ile(p.F128I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000393925
Start	111884582:111884582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.505G>C
AA Mutation	p.Gly169Arg(p.G169R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000393925
Start	111884586:111884586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs546014587
CDS Mutation	c.509G>A
AA Mutation	p.Arg170Gln(p.R170Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000393925
Start	111885320:111885320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1243A>G
AA Mutation	p.Ser415Gly(p.S415G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000393925
Start	111913485:111913485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1502G>A
AA Mutation	p.Ser501Asn(p.S501N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393925
Start	111884575:111884575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.498G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393925
Start	111940588:111940588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2340G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393925
Start	111948964:111948964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369065786
CDS Mutation	c.2520G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000393925
Start	111920368:111920368(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1952delA
AA Mutation	p.Asn651ThrfsTer4(p.N651Tfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000393925
Start	111945316:111945316(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2451delG
AA Mutation	p.Val822LeufsTer6(p.V822Lfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000393925
Start	111940553:111940553(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2309delA
AA Mutation	p.Lys770SerfsTer18(p.K770Sfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	stop_lost
Transcription ID	ENST00000393925
Start	111974563:111974563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3762G>C
AA Mutation	p.Ter1254TyrextTer1(p.1254Yext1)
Mutation Classification	Nonstop_Mutation
Feature Type	Transcript