Primary Site >> Stomach Cancer

Gene >> GALR2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000329003
Start 76077145:76077145(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs569895534
CDS Mutation c.878C>T
AA Mutation p.Ala293Val(p.A293V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000329003
Start 76075050:76075050(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.167C>T
AA Mutation p.Ala56Val(p.A56V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000329003
Start 76075217:76075217(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.334A>G
AA Mutation p.Ser112Gly(p.S112G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000329003
Start 76076851:76076851(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760705102
CDS Mutation c.584G>A
AA Mutation p.Ser195Asn(p.S195N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000329003
Start 76076889:76076889(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs142971884
CDS Mutation c.622G>A
AA Mutation p.Ala208Thr(p.A208T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000329003
Start 76077028:76077028(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759763601
CDS Mutation c.761C>T
AA Mutation p.Ala254Val(p.A254V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000329003
Start 76076992:76076992(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.725C>T
AA Mutation p.Ala242Val(p.A242V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000329003
Start 76077228:76077228(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.961C>T
AA Mutation p.Arg321Cys(p.R321C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000329003
Start 76077300:76077300(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1033A>G
AA Mutation p.Met345Val(p.M345V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000329003
Start 76077288:76077288(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1021G>A
AA Mutation p.Asp341Asn(p.D341N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000329003
Start 76076716:76076716(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.453delG
AA Mutation p.Leu152CysfsTer10(p.L152Cfs*10)
Mutation Classification Frame_Shift_Del
Feature Type Transcript