Mutation

Primary Site >> Stomach Cancer

Gene >> IL23R

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000347310
Start	67259058:67259058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1820C>A
AA Mutation	p.Ser607Tyr(p.S607Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000347310
Start	67255877:67255877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1189T>C
AA Mutation	p.Tyr397His(p.Y397H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000347310
Start	67240229:67240229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1096A>T
AA Mutation	p.Met366Leu(p.M366L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000347310
Start	67200856:67200856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767358325
CDS Mutation	c.611T>C
AA Mutation	p.Met204Thr(p.M204T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000347310
Start	67182839:67182839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781262110
CDS Mutation	c.371C>T
AA Mutation	p.Pro124Leu(p.P124L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000347310
Start	67169558:67169558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753050122
CDS Mutation	c.287A>G
AA Mutation	p.His96Arg(p.H96R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000347310
Start	67258915:67258915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1677T>G
AA Mutation	p.Ser559Arg(p.S559R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347310
Start	67259062:67259062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1824T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347310
Start	67169604:67169604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.333G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347310
Start	67200875:67200875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.630G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000347310
Start	67219616:67219616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.841G>T
AA Mutation	p.Glu281Ter(p.E281*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript