Mutation

Primary Site >> Stomach Cancer

Gene >> PRDM2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000235372
Start	13749446:13749446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201537864
CDS Mutation	c.470C>T
AA Mutation	p.Ala157Val(p.A157V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000235372
Start	13780416:13780416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145695645
CDS Mutation	c.2621C>T
AA Mutation	p.Thr874Met(p.T874M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000235372
Start	13778802:13778802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1007A>T
AA Mutation	p.Glu336Val(p.E336V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000235372
Start	13781256:13781256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3461C>A
AA Mutation	p.Ser1154Tyr(p.S1154Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000235372
Start	13780206:13780206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2411A>C
AA Mutation	p.Lys804Thr(p.K804T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000235372
Start	13782426:13782426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4631T>C
AA Mutation	p.Val1544Ala(p.V1544A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000235372
Start	13731051:13731051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.61C>T
AA Mutation	p.His21Tyr(p.H21Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000235372
Start	13778726:13778726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751199033
CDS Mutation	c.931C>T
AA Mutation	p.Arg311Trp(p.R311W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000235372
Start	13780902:13780902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3107C>T
AA Mutation	p.Pro1036Leu(p.P1036L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000235372
Start	13779387:13779387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1592C>T
AA Mutation	p.Ala531Val(p.A531V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000235372
Start	13782073:13782073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4278T>A
AA Mutation	p.Asn1426Lys(p.N1426K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000235372
Start	13782030:13782030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4235T>C
AA Mutation	p.Met1412Thr(p.M1412T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000235372
Start	13779545:13779545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1750G>C
AA Mutation	p.Asp584His(p.D584H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000235372
Start	13779012:13779012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1217G>A
AA Mutation	p.Arg406Gln(p.R406Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000235372
Start	13780841:13780841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138768059
CDS Mutation	c.3046G>A
AA Mutation	p.Ala1016Thr(p.A1016T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000235372
Start	13779309:13779309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1514T>C
AA Mutation	p.Val505Ala(p.V505A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000235372
Start	13779395:13779395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1600A>G
AA Mutation	p.Thr534Ala(p.T534A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000235372
Start	13780712:13780712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2917C>T
AA Mutation	p.Pro973Ser(p.P973S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000235372
Start	13782341:13782341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757221593
CDS Mutation	c.4546C>T
AA Mutation	p.Arg1516Trp(p.R1516W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000235372
Start	13780577:13780577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752684354
CDS Mutation	c.2782G>A
AA Mutation	p.Gly928Ser(p.G928S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000235372
Start	13780772:13780772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150941804
CDS Mutation	c.2977G>A
AA Mutation	p.Val993Ile(p.V993I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000235372
Start	13779359:13779359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148030242
CDS Mutation	c.1564G>C
AA Mutation	p.Glu522Gln(p.E522Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000235372
Start	13779293:13779293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1498C>T
AA Mutation	p.Arg500Trp(p.R500W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000235372
Start	13778877:13778877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1082C>T
AA Mutation	p.Pro361Leu(p.P361L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000235372
Start	13779011:13779011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1216C>T
AA Mutation	p.Arg406Trp(p.R406W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000235372
Start	13781941:13781941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199921095
CDS Mutation	c.4146C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000235372
Start	13780648:13780648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2853G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000235372
Start	13782724:13782724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4929G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000235372
Start	13781815:13781815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4020A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000235372
Start	13781989:13781989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4194A>T
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000235372
Start	13816445:13816445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777213855
CDS Mutation	c.5055G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000235372
Start	13782106:13782106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4311C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000235372
Start	13781587:13781587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3792T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000235372
Start	13731071:13731071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758175722
CDS Mutation	c.81G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000235372
Start	13778671:13778671(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.880delG
AA Mutation	p.Glu294LysfsTer12(p.E294Kfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	36
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000235372
Start	13780751:13780751(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2960delC
AA Mutation	p.Pro987LeufsTer54(p.P987Lfs*54)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	37
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000235372
Start	13782065:13782065(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.4277delA
AA Mutation	p.Asn1426IlefsTer3(p.N1426Ifs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	38
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000235372
Start	13779512:13779512(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1720delA
AA Mutation	p.Ile574PhefsTer12(p.I574Ffs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	39
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000235372
Start	13782563:13782563(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4773delA
AA Mutation	p.Lys1591AsnfsTer23(p.K1591Nfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	40
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000235372
Start	13781397:13781398(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3608dupT
AA Mutation	p.Leu1203PhefsTer15(p.L1203Ffs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	41
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000235372
Start	13780105:13780106(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2316dupA
AA Mutation	p.Ser773IlefsTer19(p.S773Ifs*19)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript