Mutation

Primary Site >> Stomach Cancer

Gene >> RIMS1

ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000521978
Start	72390736:72390736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4505A>C
AA Mutation	p.Asn1502Thr(p.N1502T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000521978
Start	72390717:72390717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4486A>G
AA Mutation	p.Ser1496Gly(p.S1496G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000521978
Start	72251252:72251252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2582A>G
AA Mutation	p.Glu861Gly(p.E861G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000521978
Start	72182348:72182348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.877G>A
AA Mutation	p.Val293Met(p.V293M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000521978
Start	71887064:71887064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.41C>T
AA Mutation	p.Thr14Met(p.T14M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000521978
Start	71969003:71969003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769975046
CDS Mutation	c.185C>T
AA Mutation	p.Ala62Val(p.A62V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000521978
Start	72266045:72266045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3394G>A
AA Mutation	p.Glu1132Lys(p.E1132K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000521978
Start	72399087:72399087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4853T>C
AA Mutation	p.Val1618Ala(p.V1618A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000521978
Start	72179738:72179738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.635T>A
AA Mutation	p.Leu212His(p.L212H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000521978
Start	72265000:72265000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3142T>G
AA Mutation	p.Leu1048Val(p.L1048V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000521978
Start	72251273:72251273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2603A>G
AA Mutation	p.Gln868Arg(p.Q868R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000521978
Start	71969029:71969029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.211A>G
AA Mutation	p.Arg71Gly(p.R71G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000521978
Start	72245826:72245826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746162365
CDS Mutation	c.2093G>A
AA Mutation	p.Arg698Gln(p.R698Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000521978
Start	72259111:72259111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3053G>T
AA Mutation	p.Ser1018Ile(p.S1018I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000521978
Start	72179600:72179600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753531827
CDS Mutation	c.497G>A
AA Mutation	p.Arg166Gln(p.R166Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000521978
Start	72274359:72274359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3409T>C
AA Mutation	p.Ser1137Pro(p.S1137P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000521978
Start	72097158:72097158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.455A>G
AA Mutation	p.Asn152Ser(p.N152S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000521978
Start	72399014:72399014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4780A>G
AA Mutation	p.Arg1594Gly(p.R1594G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000521978
Start	71887037:71887037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.14T>C
AA Mutation	p.Val5Ala(p.V5A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000521978
Start	72248020:72248020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2134A>C
AA Mutation	p.Ser712Arg(p.S712R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000521978
Start	72179726:72179726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.623A>T
AA Mutation	p.Lys208Met(p.K208M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000521978
Start	72182967:72182967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1496A>G
AA Mutation	p.Asp499Gly(p.D499G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000521978
Start	72333809:72333809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4340G>A
AA Mutation	p.Arg1447Lys(p.R1447K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000521978
Start	72392704:72392704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746893761
CDS Mutation	c.4512A>G
AA Mutation	p.Ile1504Met(p.I1504M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000521978
Start	72097116:72097116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.413A>C
AA Mutation	p.Lys138Thr(p.K138T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000521978
Start	72183014:72183014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1543A>G
AA Mutation	p.Lys515Glu(p.K515E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000521978
Start	72313654:72313654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs62407506
CDS Mutation	c.4112G>A
AA Mutation	p.Arg1371His(p.R1371H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000521978
Start	72258227:72258227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373238402
CDS Mutation	c.2873G>A
AA Mutation	p.Arg958His(p.R958H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000521978
Start	72290729:72290729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3605C>A
AA Mutation	p.Thr1202Asn(p.T1202N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	30
Mutation Consequence	missense_variant
Transcription ID	ENST00000521978
Start	72290818:72290818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3694C>A
AA Mutation	p.Leu1232Ile(p.L1232I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	31
Mutation Consequence	missense_variant
Transcription ID	ENST00000521978
Start	72258130:72258130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2776T>C
AA Mutation	p.Tyr926His(p.Y926H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	32
Mutation Consequence	missense_variant
Transcription ID	ENST00000521978
Start	72097013:72097013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.310C>T
AA Mutation	p.Arg104Cys(p.R104C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	33
Mutation Consequence	missense_variant
Transcription ID	ENST00000521978
Start	72179726:72179726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.623A>C
AA Mutation	p.Lys208Thr(p.K208T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	34
Mutation Consequence	missense_variant
Transcription ID	ENST00000521978
Start	72245847:72245847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2114C>T
AA Mutation	p.Pro705Leu(p.P705L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000521978
Start	71969029:71969029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.211A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000521978
Start	72290838:72290838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373917034
CDS Mutation	c.3714G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000521978
Start	72307316:72307316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3909G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	38
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000521978
Start	72265026:72265026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3168G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	39
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000521978
Start	72182347:72182347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776775023
CDS Mutation	c.876C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	40
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000521978
Start	72274421:72274421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374938269
CDS Mutation	c.3471G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	41
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000521978
Start	72182372:72182372(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.901delG
AA Mutation	p.Val301TrpfsTer61(p.V301Wfs*61)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	42
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000521978
Start	72313582:72313582(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4042delT
AA Mutation	p.Ser1348ProfsTer49(p.S1348Pfs*49)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	43
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000521978
Start	72237834:72237834(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1873delA
AA Mutation	p.Met625Ter(p.M625*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	44
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000521978
Start	72398275:72398275(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4649delA
AA Mutation	p.Lys1550ArgfsTer4(p.K1550Rfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	45
Mutation Consequence	stop_gained
Transcription ID	ENST00000521978
Start	72307278:72307278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3871C>T
AA Mutation	p.Arg1291Ter(p.R1291*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript