Primary Site >> Stomach Cancer

Gene >> ATP2C1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000507488
Start 131016198:131016198(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375974705
CDS Mutation c.2873C>A
AA Mutation p.Pro958His(p.P958H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000428331
Start 130932068:130932068(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778339531
CDS Mutation c.164G>A
AA Mutation p.Arg55Gln(p.R55Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000428331
Start 130997653:130997653(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2291G>A
AA Mutation p.Arg764His(p.R764H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000428331
Start 130964077:130964077(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774028528
CDS Mutation c.1006C>T
AA Mutation p.Pro336Ser(p.P336S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000428331
Start 130979416:130979416(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1738A>G
AA Mutation p.Ile580Val(p.I580V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000428331
Start 130937440:130937440(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs142366167
CDS Mutation c.337G>A
AA Mutation p.Val113Ile(p.V113I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000428331
Start 130930423:130930423(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs141384562
CDS Mutation c.14G>A
AA Mutation p.Arg5His(p.R5H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000428331
Start 130975465:130975465(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs756074470
CDS Mutation c.1547G>A
AA Mutation p.Arg516His(p.R516H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000428331
Start 130997749:130997749(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2387G>A
AA Mutation p.Arg796His(p.R796H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000428331
Start 130941649:130941649(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.481G>A
AA Mutation p.Val161Ile(p.V161I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000428331
Start 130998344:130998344(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2442C>T
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000428331
Start 130964991:130964991(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1068G>A
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000428331
Start 130930478:130930478(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.75delA
AA Mutation p.Ala26GlnfsTer21(p.A26Qfs*21)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000428331
Start 130930477:130930478(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.75dupA
AA Mutation p.Ala26SerfsTer3(p.A26Sfs*3)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 15
Mutation Consequence splice_donor_variant
Transcription ID ENST00000428331
Start 130969397:130969397(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1413+1G>A
Mutation Classification Splice_Site
Feature Type Transcript