Primary Site >> Stomach Cancer

Gene >> TYR

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000263321
Start 89178236:89178236(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.283T>C
AA Mutation p.Phe95Leu(p.F95L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000263321
Start 89178758:89178758(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.805T>G
AA Mutation p.Phe269Val(p.F269V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000263321
Start 89178207:89178207(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.254A>G
AA Mutation p.Tyr85Cys(p.Y85C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000263321
Start 89178488:89178488(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.535A>T
AA Mutation p.Met179Leu(p.M179L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000263321
Start 89191339:89191339(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.957A>C
AA Mutation p.Glu319Asp(p.E319D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000263321
Start 89295253:89295253(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs146020203
CDS Mutation c.1477G>T
AA Mutation p.Ala493Ser(p.A493S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000263321
Start 89227872:89227872(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1086G>A
AA Mutation p.Met362Ile(p.M362I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000263321
Start 89227948:89227948(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1162C>A
AA Mutation p.Leu388Ile(p.L388I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000263321
Start 89295186:89295186(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1410A>C
AA Mutation p.Gln470His(p.Q470H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000263321
Start 89178752:89178752(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.799T>A
AA Mutation p.Ser267Thr(p.S267T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000263321
Start 89284838:89284838(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1250C>A
AA Mutation p.Pro417His(p.P417H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000263321
Start 89178415:89178415(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.462G>A
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000263321
Start 89191324:89191324(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.942T>G
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000263321
Start 89178637:89178637(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.684T>C
Mutation Classification Silent
Feature Type Transcript
ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000263321
Start 89178535:89178535(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.582C>T
Mutation Classification Silent
Feature Type Transcript
ID 16
Mutation Consequence synonymous_variant
Transcription ID ENST00000263321
Start 89295246:89295246(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1470C>A
Mutation Classification Silent
Feature Type Transcript
ID 17
Mutation Consequence frameshift_variant
Transcription ID ENST00000263321
Start 89178353:89178353(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.405delT
AA Mutation p.Phe135LeufsTer6(p.F135Lfs*6)
Mutation Classification Frame_Shift_Del
Feature Type Transcript