Mutation

Primary Site >> Stomach Cancer

Gene >> TPX2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300403
Start	31775870:31775870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.612G>T
AA Mutation	p.Gln204His(p.Q204H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000300403
Start	31778869:31778869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.939G>T
AA Mutation	p.Lys313Asn(p.K313N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000300403
Start	31783849:31783849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1341G>T
AA Mutation	p.Lys447Asn(p.K447N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000300403
Start	31794011:31794011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1673T>C
AA Mutation	p.Leu558Pro(p.L558P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000300403
Start	31782332:31782332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1138G>A
AA Mutation	p.Ala380Thr(p.A380T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000300403
Start	31782280:31782280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1086G>C
AA Mutation	p.Lys362Asn(p.K362N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300403
Start	31782325:31782325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1131T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300403
Start	31771668:31771668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764868274
CDS Mutation	c.594T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300403
Start	31793856:31793856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759746158
CDS Mutation	c.1518C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300403
Start	31757497:31757497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.21T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000300403
Start	31782391:31782391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1196+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	12
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000300403
Start	31793990:31793992(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1654_1656delGAG
AA Mutation	p.Glu552del(p.E552del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript