Mutation

Primary Site >> Stomach Cancer

Gene >> SLC18A2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000298472
Start	117255300:117255300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754569594
CDS Mutation	c.724C>T
AA Mutation	p.Leu242Phe(p.L242F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000298472
Start	117254413:117254413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755134504
CDS Mutation	c.616A>G
AA Mutation	p.Met206Val(p.M206V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000298472
Start	117241721:117241721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.28C>T
AA Mutation	p.Arg10Cys(p.R10C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000298472
Start	117244004:117244004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.155A>C
AA Mutation	p.Lys52Thr(p.K52T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000298472
Start	117244103:117244103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775978426
CDS Mutation	c.254C>T
AA Mutation	p.Ser85Leu(p.S85L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000298472
Start	117267705:117267705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1155A>G
AA Mutation	p.Ile385Met(p.I385M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298472
Start	117241705:117241705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.12C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298472
Start	117257834:117257834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.933G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298472
Start	117255290:117255290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs549412168
CDS Mutation	c.714C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298472
Start	117241780:117241780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765162962
CDS Mutation	c.87G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000298472
Start	117254131:117254131(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.607+1delG
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000298472
Start	117255281:117255281(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.711delC
AA Mutation	p.Phe238SerfsTer48(p.F238Sfs*48)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000298472
Start	117270456:117270456(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1438delA
AA Mutation	p.Met480TrpfsTer26(p.M480Wfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript