Mutation

Primary Site >> Liver Cancer

Gene >> PTPRT

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373187
Start	42352235:42352235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1611C>G
AA Mutation	p.Ser537Arg(p.S537R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373187
Start	42350676:42350676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1817C>A
AA Mutation	p.Thr606Asn(p.T606N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373187
Start	42085841:42085841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3859T>C
AA Mutation	p.Tyr1287His(p.Y1287H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373187
Start	42199314:42199314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2417A>T
AA Mutation	p.Lys806Ile(p.K806I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000373187
Start	42315889:42315889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1973T>A
AA Mutation	p.Leu658His(p.L658H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000373187
Start	42791231:42791231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.450G>T
AA Mutation	p.Glu150Asp(p.E150D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000373187
Start	42315724:42315724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2138G>A
AA Mutation	p.Gly713Glu(p.G713E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373187
Start	42352094:42352094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1752C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373187
Start	42472480:42472480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376152261
CDS Mutation	c.1236C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373187
Start	42350711:42350711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377291418
CDS Mutation	c.1782C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000373187
Start	42161373:42161373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2661C>A
AA Mutation	p.Tyr887Ter(p.Y887*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000373187
Start	42677956:42677956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1063G>T
AA Mutation	p.Glu355Ter(p.E355*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373187
Start	42102154:42102155(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3682_3683dupTC
AA Mutation	p.Ser1229ProfsTer9(p.S1229Pfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript