Primary Site >> Stomach Cancer

Gene >> FADS2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000278840
Start 61848187:61848187(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.647G>A
AA Mutation p.Arg216His(p.R216H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000278840
Start 61857018:61857018(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.752A>G
AA Mutation p.Lys251Arg(p.K251R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000278840
Start 61837785:61837785(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.215T>C
AA Mutation p.Phe72Ser(p.F72S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000278840
Start 61848204:61848204(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs199900021
CDS Mutation c.664G>A
AA Mutation p.Ala222Thr(p.A222T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000278840
Start 61857458:61857458(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.810G>C
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000278840
Start 61828558:61828558(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.168C>G
Mutation Classification Silent
Feature Type Transcript