Primary Site >> Stomach Cancer

Gene >> IRX1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000302006
Start 3599765:3599765(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.817G>A
AA Mutation p.Asp273Asn(p.D273N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000302006
Start 3600620:3600620(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1324G>A
AA Mutation p.Val442Ile(p.V442I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000302006
Start 3599644:3599644(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.696G>C
AA Mutation p.Lys232Asn(p.K232N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000302006
Start 3599343:3599343(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.395A>C
AA Mutation p.Lys132Thr(p.K132T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000302006
Start 3599387:3599387(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.439A>G
AA Mutation p.Asn147Asp(p.N147D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000302006
Start 3600638:3600638(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1342C>T
AA Mutation p.Pro448Ser(p.P448S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000302006
Start 3599309:3599309(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.361G>A
AA Mutation p.Gly121Ser(p.G121S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000302006
Start 3599794:3599794(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777640998
CDS Mutation c.846G>T
AA Mutation p.Leu282Phe(p.L282F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000302006
Start 3600669:3600669(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1373C>T
AA Mutation p.Pro458Leu(p.P458L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000302006
Start 3600128:3600128(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1180G>A
AA Mutation p.Val394Ile(p.V394I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000302006
Start 3599768:3599768(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755172641
CDS Mutation c.820G>A
AA Mutation p.Val274Ile(p.V274I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000302006
Start 3596356:3596356(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.251C>T
AA Mutation p.Ala84Val(p.A84V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000302006
Start 3599633:3599633(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.685G>A
AA Mutation p.Asp229Asn(p.D229N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000302006
Start 3599501:3599501(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.553C>T
AA Mutation p.Leu185Phe(p.L185F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000302006
Start 3596299:3596299(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.194C>T
AA Mutation p.Ala65Val(p.A65V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000302006
Start 3600221:3600221(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1273G>A
AA Mutation p.Gly425Arg(p.G425R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000302006
Start 3599474:3599474(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.526A>G
AA Mutation p.Thr176Ala(p.T176A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000302006
Start 3600165:3600165(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1217T>G
AA Mutation p.Leu406Arg(p.L406R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000302006
Start 3599589:3599589(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.641C>T
AA Mutation p.Pro214Leu(p.P214L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000302006
Start 3600080:3600080(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1132G>A
AA Mutation p.Ala378Thr(p.A378T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000302006
Start 3599648:3599648(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.700G>A
AA Mutation p.Asp234Asn(p.D234N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 22
Mutation Consequence synonymous_variant
Transcription ID ENST00000302006
Start 3600637:3600637(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1341G>T
Mutation Classification Silent
Feature Type Transcript
ID 23
Mutation Consequence synonymous_variant
Transcription ID ENST00000302006
Start 3599707:3599707(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.759C>T
Mutation Classification Silent
Feature Type Transcript
ID 24
Mutation Consequence synonymous_variant
Transcription ID ENST00000302006
Start 3600995:3600995(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1398G>A
Mutation Classification Silent
Feature Type Transcript
ID 25
Mutation Consequence synonymous_variant
Transcription ID ENST00000302006
Start 3599995:3599995(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1047G>A
Mutation Classification Silent
Feature Type Transcript
ID 26
Mutation Consequence synonymous_variant
Transcription ID ENST00000302006
Start 3599608:3599608(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.660C>T
Mutation Classification Silent
Feature Type Transcript
ID 27
Mutation Consequence synonymous_variant
Transcription ID ENST00000302006
Start 3599356:3599356(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.408C>T
Mutation Classification Silent
Feature Type Transcript
ID 28
Mutation Consequence synonymous_variant
Transcription ID ENST00000302006
Start 3601007:3601007(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1410G>A
Mutation Classification Silent
Feature Type Transcript
ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000302006
Start 3599296:3599296(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.348T>G
Mutation Classification Silent
Feature Type Transcript
ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000302006
Start 3599296:3599296(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.348T>C
Mutation Classification Silent
Feature Type Transcript