Mutation

Primary Site >> Stomach Cancer

Gene >> IFT122

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000348417
Start	129502832:129502832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2497G>A
AA Mutation	p.Asp833Asn(p.D833N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000348417
Start	129476436:129476436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376018883
CDS Mutation	c.938G>A
AA Mutation	p.Arg313Gln(p.R313Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000348417
Start	129476684:129476684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1030A>G
AA Mutation	p.Thr344Ala(p.T344A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000348417
Start	129507759:129507759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2883C>G
AA Mutation	p.His961Gln(p.H961Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000348417
Start	129476474:129476474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.976A>G
AA Mutation	p.Thr326Ala(p.T326A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000348417
Start	129476714:129476714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1060A>G
AA Mutation	p.Thr354Ala(p.T354A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000348417
Start	129514397:129514397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2996T>A
AA Mutation	p.Leu999His(p.L999H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000348417
Start	129512394:129512394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2969C>T
AA Mutation	p.Pro990Leu(p.P990L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000348417
Start	129478175:129478175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1307G>A
AA Mutation	p.Cys436Tyr(p.C436Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000348417
Start	129495582:129495582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2183A>G
AA Mutation	p.Asp728Gly(p.D728G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000348417
Start	129502724:129502724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376362722
CDS Mutation	c.2389G>A
AA Mutation	p.Ala797Thr(p.A797T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000348417
Start	129507701:129507701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2825T>G
AA Mutation	p.Phe942Cys(p.F942C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000348417
Start	129483590:129483590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774723842
CDS Mutation	c.1759C>T
AA Mutation	p.Arg587Trp(p.R587W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000348417
Start	129461265:129461265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755585099
CDS Mutation	c.310A>G
AA Mutation	p.Ile104Val(p.I104V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000348417
Start	129502769:129502769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201800117
CDS Mutation	c.2434G>A
AA Mutation	p.Ala812Thr(p.A812T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000348417
Start	129519718:129519718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3622C>A
AA Mutation	p.Pro1208Thr(p.P1208T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000348417
Start	129483601:129483601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1770G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000348417
Start	129466932:129466932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs181789156
CDS Mutation	c.606C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000348417
Start	129514431:129514431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3030T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000348417
Start	129467058:129467058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202074599
CDS Mutation	c.732C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000348417
Start	129476389:129476389(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs778534085
CDS Mutation	c.896delG
AA Mutation	p.Gly299ValfsTer71(p.G299Vfs*71)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000348417
Start	129512391:129512391(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2970delC
AA Mutation	p.Ser991ArgfsTer6(p.S991Rfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000348417
Start	129492165:129492165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2017C>T
AA Mutation	p.Arg673Ter(p.R673*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript