Mutation

Primary Site >> Stomach Cancer

Gene >> MTTP

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265517
Start	99589706:99589706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.457G>T
AA Mutation	p.Ala153Ser(p.A153S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265517
Start	99600699:99600699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1202C>A
AA Mutation	p.Ser401Tyr(p.S401Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265517
Start	99611153:99611153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs561968572
CDS Mutation	c.1780C>T
AA Mutation	p.Arg594Cys(p.R594C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265517
Start	99601657:99601657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1287G>A
AA Mutation	p.Met429Ile(p.M429I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265517
Start	99606865:99606865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1462A>G
AA Mutation	p.Ser488Gly(p.S488G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265517
Start	99622747:99622747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760443132
CDS Mutation	c.2584G>A
AA Mutation	p.Val862Ile(p.V862I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265517
Start	99591323:99591323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs137997894
CDS Mutation	c.590C>T
AA Mutation	p.Ala197Val(p.A197V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265517
Start	99581940:99581940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.97C>A
AA Mutation	p.Leu33Met(p.L33M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000265517
Start	99608937:99608937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1729G>A
AA Mutation	p.Ala577Thr(p.A577T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000265517
Start	99608827:99608827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199422220
CDS Mutation	c.1619G>A
AA Mutation	p.Arg540His(p.R540H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265517
Start	99594775:99594775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.801G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265517
Start	99619069:99619069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2313T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265517
Start	99601696:99601696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1326T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265517
Start	99613059:99613059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2136T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265517
Start	99574929:99574929(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.24delT
AA Mutation	p.Leu9SerfsTer20(p.L9Sfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript