Primary Site >> Stomach Cancer

Gene >> MARK2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000402010
Start 63904042:63904042(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs373710920
CDS Mutation c.1571C>T
AA Mutation p.Ala524Val(p.A524V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000402010
Start 63902291:63902291(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs756086174
CDS Mutation c.1195G>A
AA Mutation p.Val399Met(p.V399M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000402010
Start 63898814:63898814(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.455C>T
AA Mutation p.Ala152Val(p.A152V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000402010
Start 63902258:63902258(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1162G>A
AA Mutation p.Ala388Thr(p.A388T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000402010
Start 63899980:63899980(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.638C>T
AA Mutation p.Pro213Leu(p.P213L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000402010
Start 63899099:63899099(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.522A>C
AA Mutation p.Arg174Ser(p.R174S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000402010
Start 63908909:63908909(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2039A>C
AA Mutation p.Lys680Thr(p.K680T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000402010
Start 63904890:63904890(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1781G>A
AA Mutation p.Arg594Gln(p.R594Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000402010
Start 63902685:63902685(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1319A>G
AA Mutation p.Asp440Gly(p.D440G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000402010
Start 63904996:63904996(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745421643
CDS Mutation c.1887G>A
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000402010
Start 63904798:63904798(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1689G>A
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000402010
Start 63902623:63902623(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1257C>A
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000402010
Start 63904791:63904791(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1687delC
AA Mutation p.Gln563SerfsTer53(p.Q563Sfs*53)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000402010
Start 63904992:63904992(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1888delG
AA Mutation p.Ala630ProfsTer27(p.A630Pfs*27)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000402010
Start 63902772:63902772(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1410delC
AA Mutation p.Ser471ProfsTer36(p.S471Pfs*36)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 16
Mutation Consequence frameshift_variant
Transcription ID ENST00000402010
Start 63895245:63895246(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.145dupC
AA Mutation p.His49ProfsTer15(p.H49Pfs*15)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 17
Mutation Consequence inframe_deletion
Transcription ID ENST00000402010
Start 63899966:63899968(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.626_628delTCT
AA Mutation p.Phe209del(p.F209del)
Mutation Classification In_Frame_Del
Feature Type Transcript