Primary Site >> Stomach Cancer

Gene >> ABCC9

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000261201
Start 21852110:21852110(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2756A>G
AA Mutation p.Gln919Arg(p.Q919R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000261201
Start 21936569:21936569(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.106T>G
AA Mutation p.Phe36Val(p.F36V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000261201
Start 21872722:21872722(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2101A>C
AA Mutation p.Thr701Pro(p.T701P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000261201
Start 21842444:21842444(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3343A>C
AA Mutation p.Thr1115Pro(p.T1115P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000261201
Start 21809884:21809884(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4283A>T
AA Mutation p.Lys1428Met(p.K1428M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000261201
Start 21817274:21817274(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3805T>A
AA Mutation p.Leu1269Met(p.L1269M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000261201
Start 21859617:21859617(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2474C>T
AA Mutation p.Ala825Val(p.A825V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000261201
Start 21910206:21910206(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1271T>C
AA Mutation p.Leu424Pro(p.L424P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000261201
Start 21845716:21845716(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374500043
CDS Mutation c.2983A>G
AA Mutation p.Ile995Val(p.I995V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000261201
Start 21916968:21916968(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.542T>C
AA Mutation p.Met181Thr(p.M181T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000261201
Start 21882871:21882871(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1914G>T
AA Mutation p.Gln638His(p.Q638H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000261201
Start 21852119:21852119(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2747G>A
AA Mutation p.Arg916Gln(p.R916Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000261201
Start 21844520:21844520(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3278T>C
AA Mutation p.Leu1093Pro(p.L1093P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000261201
Start 21910833:21910833(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1157C>T
AA Mutation p.Ala386Val(p.A386V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000261201
Start 21812125:21812125(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4135A>G
AA Mutation p.Lys1379Glu(p.K1379E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000261201
Start 21845736:21845736(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2963C>A
AA Mutation p.Ser988Tyr(p.S988Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000261201
Start 21829038:21829038(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778849288
CDS Mutation c.3589C>T
AA Mutation p.Arg1197Cys(p.R1197C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000261201
Start 21916963:21916963(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.547G>A
AA Mutation p.Val183Met(p.V183M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000261201
Start 21815849:21815849(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3937A>G
AA Mutation p.Lys1313Glu(p.K1313E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000261201
Start 21915817:21915817(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.667C>A
AA Mutation p.Leu223Met(p.L223M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000261201
Start 21817274:21817274(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3805T>G
AA Mutation p.Leu1269Val(p.L1269V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000261201
Start 21844508:21844508(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3290C>T
AA Mutation p.Ser1097Leu(p.S1097L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000261201
Start 21872679:21872679(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2144T>C
AA Mutation p.Leu715Pro(p.L715P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000261201
Start 21842406:21842406(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3381G>A
AA Mutation p.Met1127Ile(p.M1127I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000261201
Start 21894158:21894158(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772619542
CDS Mutation c.1676C>T
AA Mutation p.Ala559Val(p.A559V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000261201
Start 21805281:21805281(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4543C>G
AA Mutation p.Leu1515Val(p.L1515V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000261201
Start 21848159:21848159(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs143685061
CDS Mutation c.2857G>A
AA Mutation p.Glu953Lys(p.E953K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000261201
Start 21917026:21917026(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.484A>C
AA Mutation p.Ile162Leu(p.I162L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000261201
Start 21882792:21882792(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200891785
CDS Mutation c.1993G>A
AA Mutation p.Ala665Thr(p.A665T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000261201
Start 21912912:21912912(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.971G>A
AA Mutation p.Arg324His(p.R324H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000261201
Start 21908190:21908190(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1342C>T
AA Mutation p.Leu448Phe(p.L448F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 32
Mutation Consequence missense_variant
Transcription ID ENST00000261201
Start 21844867:21844867(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3145C>A
AA Mutation p.Leu1049Ile(p.L1049I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 33
Mutation Consequence missense_variant
Transcription ID ENST00000261201
Start 21852466:21852466(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2545C>A
AA Mutation p.His849Asn(p.H849N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 34
Mutation Consequence missense_variant
Transcription ID ENST00000261201
Start 21926023:21926023(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374849789
CDS Mutation c.325G>A
AA Mutation p.Val109Met(p.V109M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 35
Mutation Consequence missense_variant
Transcription ID ENST00000261201
Start 21852150:21852150(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2716C>A
AA Mutation p.Leu906Ile(p.L906I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 36
Mutation Consequence missense_variant
Transcription ID ENST00000261201
Start 21805308:21805308(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4516C>A
AA Mutation p.Arg1506Ser(p.R1506S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 37
Mutation Consequence missense_variant
Transcription ID ENST00000261201
Start 21845827:21845827(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2872G>A
AA Mutation p.Glu958Lys(p.E958K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 38
Mutation Consequence missense_variant
Transcription ID ENST00000261201
Start 21805214:21805214(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4610A>C
AA Mutation p.Lys1537Thr(p.K1537T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 39
Mutation Consequence missense_variant
Transcription ID ENST00000261201
Start 21817220:21817220(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3859A>G
AA Mutation p.Thr1287Ala(p.T1287A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 40
Mutation Consequence missense_variant
Transcription ID ENST00000261201
Start 21908121:21908121(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1411T>C
AA Mutation p.Tyr471His(p.Y471H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 41
Mutation Consequence missense_variant
Transcription ID ENST00000261201
Start 21812148:21812148(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4112T>C
AA Mutation p.Val1371Ala(p.V1371A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 42
Mutation Consequence synonymous_variant
Transcription ID ENST00000261201
Start 21863015:21863015(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2277T>C
Mutation Classification Silent
Feature Type Transcript
ID 43
Mutation Consequence synonymous_variant
Transcription ID ENST00000261201
Start 21829012:21829012(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs17846779
CDS Mutation c.3615C>T
Mutation Classification Silent
Feature Type Transcript
ID 44
Mutation Consequence synonymous_variant
Transcription ID ENST00000261201
Start 21852127:21852127(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2739T>C
Mutation Classification Silent
Feature Type Transcript
ID 45
Mutation Consequence synonymous_variant
Transcription ID ENST00000261201
Start 21887862:21887862(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs727502873
CDS Mutation c.1875G>A
Mutation Classification Silent
Feature Type Transcript
ID 46
Mutation Consequence synonymous_variant
Transcription ID ENST00000261201
Start 21882832:21882832(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1953C>T
Mutation Classification Silent
Feature Type Transcript
ID 47
Mutation Consequence synonymous_variant
Transcription ID ENST00000261201
Start 21852413:21852413(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2598C>T
Mutation Classification Silent
Feature Type Transcript
ID 48
Mutation Consequence synonymous_variant
Transcription ID ENST00000261201
Start 21805270:21805270(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4554C>T
Mutation Classification Silent
Feature Type Transcript
ID 49
Mutation Consequence synonymous_variant
Transcription ID ENST00000261201
Start 21872636:21872636(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2187T>C
Mutation Classification Silent
Feature Type Transcript
ID 50
Mutation Consequence frameshift_variant
Transcription ID ENST00000261201
Start 21915762:21915762(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.722delA
AA Mutation p.Lys241SerfsTer5(p.K241Sfs*5)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 51
Mutation Consequence frameshift_variant
Transcription ID ENST00000261201
Start 21844546:21844546(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.3252delT
AA Mutation p.Phe1084LeufsTer8(p.F1084Lfs*8)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 52
Mutation Consequence stop_gained
Transcription ID ENST00000261201
Start 21859621:21859621(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2470C>T
AA Mutation p.Arg824Ter(p.R824*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 53
Mutation Consequence frameshift_variant
Transcription ID ENST00000261201
Start 21906234:21906235(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1509dupA
AA Mutation p.Leu504ThrfsTer25(p.L504Tfs*25)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript