Primary Site >> Stomach Cancer

Gene >> FGF10

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000264664
Start 44388448:44388448(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.235T>G
AA Mutation p.Trp79Gly(p.W79G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000264664
Start 44388537:44388537(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751081612
CDS Mutation c.146C>T
AA Mutation p.Ala49Val(p.A49V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000264664
Start 44310462:44310462(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.394T>G
AA Mutation p.Leu132Val(p.L132V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000264664
Start 44305090:44305090(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.532G>A
AA Mutation p.Val178Met(p.V178M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000264664
Start 44388669:44388669(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.14T>G
AA Mutation p.Ile5Arg(p.I5R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000264664
Start 44388538:44388538(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.145G>A
AA Mutation p.Ala49Thr(p.A49T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000264664
Start 44305026:44305026(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.596C>T
AA Mutation p.Ala199Val(p.A199V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000264664
Start 44388371:44388371(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.312G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000264664
Start 44388362:44388362(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.321G>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000264664
Start 44310501:44310501(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.355G>T
AA Mutation p.Gly119Ter(p.G119*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript