Primary Site >> Stomach Cancer

Gene >> ABCB7

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000373394
Start 75069397:75069397(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1423G>A
AA Mutation p.Asp475Asn(p.D475N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000373394
Start 75099006:75099006(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.389C>T
AA Mutation p.Pro130Leu(p.P130L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000373394
Start 75076542:75076542(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.566C>T
AA Mutation p.Ala189Val(p.A189V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000373394
Start 75098995:75098995(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.400C>T
AA Mutation p.Pro134Ser(p.P134S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000373394
Start 75069085:75069085(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1581T>C
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000373394
Start 75156258:75156258(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.15G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000373394
Start 75075599:75075599(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.618delT
AA Mutation p.Phe206LeufsTer12(p.F206Lfs*12)
Mutation Classification Frame_Shift_Del
Feature Type Transcript