Mutation

Primary Site >> Stomach Cancer

Gene >> MPRIP

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341712
Start	17171764:17171764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2210A>C
AA Mutation	p.Lys737Thr(p.K737T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341712
Start	17158715:17158715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1759C>T
AA Mutation	p.Arg587Trp(p.R587W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000341712
Start	17075780:17075780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773367883
CDS Mutation	c.194G>A
AA Mutation	p.Arg65Gln(p.R65Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000341712
Start	17078024:17078024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.215G>A
AA Mutation	p.Arg72Gln(p.R72Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000341712
Start	17158730:17158730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770423449
CDS Mutation	c.1774C>T
AA Mutation	p.Arg592Cys(p.R592C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000341712
Start	17175332:17175332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375924665
CDS Mutation	c.2629C>T
AA Mutation	p.Arg877Trp(p.R877W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000341712
Start	17174029:17174029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2543T>G
AA Mutation	p.Leu848Arg(p.L848R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000341712
Start	17172739:17172739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2353C>T
AA Mutation	p.Arg785Trp(p.R785W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000341712
Start	17126769:17126769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.335G>A
AA Mutation	p.Arg112His(p.R112H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000341712
Start	17150178:17150178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1310C>T
AA Mutation	p.Ala437Val(p.A437V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000341712
Start	17158602:17158602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149009201
CDS Mutation	c.1646G>A
AA Mutation	p.Arg549His(p.R549H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000341712
Start	17158946:17158946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1990G>A
AA Mutation	p.Glu664Lys(p.E664K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000341712
Start	17161333:17161333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2140G>A
AA Mutation	p.Ala714Thr(p.A714T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341712
Start	17171756:17171756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756119982
CDS Mutation	c.2202G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341712
Start	17126743:17126743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.309C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341712
Start	17154371:17154371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1431C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000341712
Start	17143572:17143572(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1058delC
AA Mutation	p.Pro353GlnfsTer30(p.P353Qfs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000341712
Start	17158513:17158513(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1561delG
AA Mutation	p.Glu521SerfsTer104(p.E521Sfs*104)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript