Primary Site >> Stomach Cancer

Gene >> GALNT5

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000259056
Start 157258729:157258729(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.647T>C
AA Mutation p.Leu216Ser(p.L216S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000259056
Start 157295782:157295782(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1861A>G
AA Mutation p.Asn621Asp(p.N621D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000259056
Start 157258294:157258294(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.212T>C
AA Mutation p.Ile71Thr(p.I71T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000259056
Start 157259341:157259341(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763670213
CDS Mutation c.1259C>T
AA Mutation p.Thr420Met(p.T420M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000259056
Start 157258689:157258689(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.607C>T
AA Mutation p.Pro203Ser(p.P203S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000259056
Start 157286065:157286065(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1672C>T
AA Mutation p.Arg558Trp(p.R558W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000259056
Start 157259409:157259409(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140478877
CDS Mutation c.1327C>T
AA Mutation p.Arg443Cys(p.R443C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000259056
Start 157258879:157258879(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.797A>T
AA Mutation p.Asn266Ile(p.N266I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000259056
Start 157259199:157259199(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1117C>A
AA Mutation p.Pro373Thr(p.P373T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000259056
Start 157311290:157311290(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2765C>T
AA Mutation p.Ala922Val(p.A922V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000259056
Start 157299622:157299622(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2072G>A
AA Mutation p.Gly691Asp(p.G691D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000259056
Start 157305761:157305761(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2452G>C
AA Mutation p.Ala818Pro(p.A818P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000259056
Start 157299616:157299616(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2066A>G
AA Mutation p.Asp689Gly(p.D689G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000259056
Start 157258211:157258211(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.129G>T
Mutation Classification Silent
Feature Type Transcript
ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000259056
Start 157259342:157259342(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776611399
CDS Mutation c.1260G>A
Mutation Classification Silent
Feature Type Transcript
ID 16
Mutation Consequence synonymous_variant
Transcription ID ENST00000259056
Start 157295742:157295742(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1821A>G
Mutation Classification Silent
Feature Type Transcript
ID 17
Mutation Consequence frameshift_variant
Transcription ID ENST00000259056
Start 157259281:157259281(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1203delC
AA Mutation p.Ser402LeufsTer9(p.S402Lfs*9)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 18
Mutation Consequence frameshift_variant
Transcription ID ENST00000259056
Start 157311220:157311221(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.2700dupT
AA Mutation p.Glu901Ter(p.E901*)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 19
Mutation Consequence frameshift_variant
Transcription ID ENST00000259056
Start 157296480:157296481(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.1970dupA
AA Mutation p.Asn657LysfsTer4(p.N657Kfs*4)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript