Mutation

Primary Site >> Stomach Cancer

Gene >> UBR5

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000520539
Start	102345539:102345539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.743T>G
AA Mutation	p.Leu248Arg(p.L248R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000520539
Start	102261931:102261931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7826A>T
AA Mutation	p.Glu2609Val(p.E2609V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000520539
Start	102311454:102311454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2461C>A
AA Mutation	p.Pro821Thr(p.P821T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000520539
Start	102281398:102281398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5818G>A
AA Mutation	p.Asp1940Asn(p.D1940N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000520539
Start	102298473:102298473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3343A>C
AA Mutation	p.Thr1115Pro(p.T1115P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000520539
Start	102285166:102285166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747984717
CDS Mutation	c.5657C>T
AA Mutation	p.Ala1886Val(p.A1886V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000520539
Start	102280403:102280403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5992A>G
AA Mutation	p.Thr1998Ala(p.T1998A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000520539
Start	102345398:102345398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.884G>A
AA Mutation	p.Arg295Gln(p.R295Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000520539
Start	102281478:102281478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5738C>T
AA Mutation	p.Ala1913Val(p.A1913V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000520539
Start	102285551:102285551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5446G>A
AA Mutation	p.Ala1816Thr(p.A1816T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000520539
Start	102286563:102286563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5012C>T
AA Mutation	p.Ser1671Leu(p.S1671L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000520539
Start	102295027:102295027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4143C>G
AA Mutation	p.Asp1381Glu(p.D1381E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000520539
Start	102285740:102285740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5257C>T
AA Mutation	p.Arg1753Cys(p.R1753C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000520539
Start	102285674:102285674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5323A>C
AA Mutation	p.Ser1775Arg(p.S1775R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000520539
Start	102311324:102311324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2591C>T
AA Mutation	p.Ala864Val(p.A864V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000520539
Start	102312212:102312212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757038576
CDS Mutation	c.2185G>A
AA Mutation	p.Asp729Asn(p.D729N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000520539
Start	102275758:102275758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6580G>A
AA Mutation	p.Glu2194Lys(p.E2194K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000520539
Start	102314788:102314788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1850G>A
AA Mutation	p.Cys617Tyr(p.C617Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000520539
Start	102281385:102281385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5831T>C
AA Mutation	p.Leu1944Ser(p.L1944S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000520539
Start	102285737:102285737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5260C>T
AA Mutation	p.Arg1754Trp(p.R1754W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000520539
Start	102300134:102300134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2972T>C
AA Mutation	p.Met991Thr(p.M991T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000520539
Start	102326658:102326658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1487T>C
AA Mutation	p.Val496Ala(p.V496A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000520539
Start	102276977:102276977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6504T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000520539
Start	102261918:102261918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7839A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000520539
Start	102270159:102270159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140195197
CDS Mutation	c.7110C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000520539
Start	102327774:102327774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1449C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000520539
Start	102346255:102346255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768814975
CDS Mutation	c.717C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000520539
Start	102299519:102299519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs548926233
CDS Mutation	c.3135C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000520539
Start	102347077:102347077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs547851962
CDS Mutation	c.402T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000520539
Start	102257698:102257698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566010702
CDS Mutation	c.8121T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000520539
Start	102360642:102360642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.213T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000520539
Start	102285678:102285678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5319C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000520539
Start	102295668:102295668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3780T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000520539
Start	102285165:102285165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145137858
CDS Mutation	c.5658G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000520539
Start	102275756:102275756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6582A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000520539
Start	102277121:102277121(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs763652408
CDS Mutation	c.6360delA
AA Mutation	p.Glu2121LysfsTer28(p.E2121Kfs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	37
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000520539
Start	102280394:102280395(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.6000_6001delAA
AA Mutation	p.Ser2001CysfsTer5(p.S2001Cfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	38
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000520539
Start	102262044:102262044(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.7713delT
AA Mutation	p.Phe2571LeufsTer4(p.F2571Lfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	39
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000520539
Start	102360165:102360165(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.292delG
AA Mutation	p.Ala98GlnfsTer23(p.A98Qfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	40
Mutation Consequence	stop_gained
Transcription ID	ENST00000520539
Start	102285742:102285742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5255T>G
AA Mutation	p.Leu1752Ter(p.L1752*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	41
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000520539
Start	102272692:102272693(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.6809_6810insTA
AA Mutation	p.Pro2271AsnfsTer8(p.P2271Nfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	42
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000520539
Start	102277113:102277114(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.6367dupG
AA Mutation	p.Glu2123GlyfsTer11(p.E2123Gfs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	43
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000520539
Start	102293995:102293996(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.4308dupT
AA Mutation	p.Val1437CysfsTer65(p.V1437Cfs*65)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	44
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000520539
Start	102312166:102312167(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2230dupA
AA Mutation	p.Thr744AsnfsTer29(p.T744Nfs*29)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript