Primary Site >> Stomach Cancer

Gene >> ATG7

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000354449
Start 11347918:11347918(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1167G>T
AA Mutation p.Lys389Asn(p.K389N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000354449
Start 11306989:11306989(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.262T>G
AA Mutation p.Tyr88Asp(p.Y88D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000354449
Start 11306945:11306945(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs557310519
CDS Mutation c.218G>A
AA Mutation p.Ser73Asn(p.S73N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000354449
Start 11342235:11342235(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1081C>A
AA Mutation p.Leu361Ile(p.L361I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000354449
Start 11298839:11298839(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.144G>T
AA Mutation p.Lys48Asn(p.K48N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000354449
Start 11364661:11364661(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1802G>A
AA Mutation p.Gly601Asp(p.G601D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000354449
Start 11340705:11340705(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.950T>C
AA Mutation p.Val317Ala(p.V317A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000354449
Start 11340659:11340659(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.904G>A
AA Mutation p.Val302Ile(p.V302I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000354449
Start 11331411:11331411(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.750C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000354449
Start 11331348:11331348(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.687T>C
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence splice_donor_variant
Transcription ID ENST00000354449
Start 11299418:11299418(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.215+2T>C
Mutation Classification Splice_Site
Feature Type Transcript