Mutation

Primary Site >> Stomach Cancer

Gene >> TSPYL5

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000322128
Start	97277810:97277810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.35G>A
AA Mutation	p.Arg12His(p.R12H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000322128
Start	97277252:97277252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.593C>T
AA Mutation	p.Thr198Met(p.T198M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000322128
Start	97277754:97277754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.91G>A
AA Mutation	p.Asp31Asn(p.D31N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000322128
Start	97277838:97277838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7G>A
AA Mutation	p.Gly3Ser(p.G3S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000322128
Start	97277405:97277405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368313628
CDS Mutation	c.440A>G
AA Mutation	p.Lys147Arg(p.K147R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000322128
Start	97276874:97276874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148712696
CDS Mutation	c.971G>A
AA Mutation	p.Arg324His(p.R324H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000322128
Start	97277517:97277517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.328G>A
AA Mutation	p.Ala110Thr(p.A110T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000322128
Start	97277255:97277255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.590C>T
AA Mutation	p.Ala197Val(p.A197V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000322128
Start	97276602:97276602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1243C>A
AA Mutation	p.Gln415Lys(p.Q415K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000322128
Start	97277421:97277421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.424C>T
AA Mutation	p.Arg142Cys(p.R142C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000322128
Start	97277190:97277190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.655G>A
AA Mutation	p.Ala219Thr(p.A219T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000322128
Start	97277400:97277400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.445G>C
AA Mutation	p.Ala149Pro(p.A149P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000322128
Start	97277439:97277439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.406C>A
AA Mutation	p.Pro136Thr(p.P136T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322128
Start	97277746:97277746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.99G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322128
Start	97277839:97277839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322128
Start	97276939:97276939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762182664
CDS Mutation	c.906G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322128
Start	97277680:97277680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.165T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000322128
Start	97277436:97277436(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.409delC
AA Mutation	p.Arg137AlafsTer27(p.R137Afs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000322128
Start	97277145:97277145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.700C>T
AA Mutation	p.Arg234Ter(p.R234*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript