Mutation

Primary Site >> Liver Cancer

Gene >> RP1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000220676
Start	54626545:54626545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2663C>G
AA Mutation	p.Ala888Gly(p.A888G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000220676
Start	54622186:54622186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.685C>T
AA Mutation	p.Pro229Ser(p.P229S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000220676
Start	54627346:54627346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3464A>G
AA Mutation	p.Asn1155Ser(p.N1155S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000220676
Start	54626722:54626722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2840G>T
AA Mutation	p.Cys947Phe(p.C947F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000220676
Start	54621540:54621540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751318405
CDS Mutation	c.574C>A
AA Mutation	p.Gln192Lys(p.Q192K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000220676
Start	54630108:54630108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6226T>A
AA Mutation	p.Phe2076Ile(p.F2076I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000220676
Start	54621234:54621234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779243716
CDS Mutation	c.268C>G
AA Mutation	p.His90Asp(p.H90D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000220676
Start	54621333:54621333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769522856
CDS Mutation	c.367C>T
AA Mutation	p.Arg123Cys(p.R123C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000220676
Start	54627993:54627993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4111G>C
AA Mutation	p.Asp1371His(p.D1371H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000220676
Start	54626779:54626779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2897A>C
AA Mutation	p.Asn966Thr(p.N966T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000220676
Start	54621520:54621520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.554A>T
AA Mutation	p.Gln185Leu(p.Q185L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220676
Start	54621389:54621389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.423C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220676
Start	54626675:54626675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2793T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000220676
Start	54626192:54626192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2310T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000220676
Start	54628655:54628655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4773G>A
AA Mutation	p.Trp1591Ter(p.W1591*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript