Mutation

Primary Site >> Stomach Cancer

Gene >> OXCT1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000196371
Start	41842696:41842696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.650G>A
AA Mutation	p.Arg217Gln(p.R217Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000196371
Start	41803148:41803148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.971G>C
AA Mutation	p.Gly324Ala(p.G324A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000196371
Start	41862716:41862716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756300300
CDS Mutation	c.113G>A
AA Mutation	p.Arg38His(p.R38H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000196371
Start	41853505:41853505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755989003
CDS Mutation	c.328C>T
AA Mutation	p.Arg110Cys(p.R110C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000196371
Start	41850159:41850159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.435C>G
AA Mutation	p.Ile145Met(p.I145M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000196371
Start	41762116:41762116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1333G>A
AA Mutation	p.Ala445Thr(p.A445T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000196371
Start	41807368:41807368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.803G>A
AA Mutation	p.Arg268His(p.R268H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000196371
Start	41850173:41850173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.421C>A
AA Mutation	p.Leu141Ile(p.L141I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000196371
Start	41739414:41739414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1497G>C
AA Mutation	p.Gln499His(p.Q499H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000196371
Start	41842764:41842764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.582T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000196371
Start	41850084:41850084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751233853
CDS Mutation	c.510G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000196371
Start	41807382:41807382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.789G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000196371
Start	41862703:41862703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.126T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000196371
Start	41794710:41794710(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1139delT
AA Mutation	p.Phe380SerfsTer9(p.F380Sfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000196371
Start	41862681:41862681(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.148delG
AA Mutation	p.Val50Ter(p.V50*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript