Primary Site >> Stomach Cancer

Gene >> SLC22A1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000366963
Start 160139809:160139809(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1218G>A
AA Mutation p.Met406Ile(p.M406I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000366963
Start 160136277:160136277(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766513281
CDS Mutation c.897A>G
AA Mutation p.Ile299Met(p.I299M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000366963
Start 160122204:160122204(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs138657404
CDS Mutation c.269G>A
AA Mutation p.Arg90His(p.R90H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000366963
Start 160134071:160134071(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780454201
CDS Mutation c.785G>A
AA Mutation p.Arg262His(p.R262H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000366963
Start 160136308:160136308(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.928G>A
AA Mutation p.Gly310Arg(p.G310R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000366963
Start 160122322:160122322(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774374480
CDS Mutation c.387G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000366963
Start 160122034:160122034(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs560595462
CDS Mutation c.99G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000366963
Start 160122022:160122022(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760852994
CDS Mutation c.87G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000366963
Start 160139794:160139794(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1203C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000366963
Start 160136255:160136255(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.880delA
AA Mutation p.Arg294GlufsTer6(p.R294Efs*6)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000366963
Start 160136233:160136234(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.857dupC
AA Mutation p.Arg287SerfsTer11(p.R287Sfs*11)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript