Mutation

Primary Site >> Stomach Cancer

Gene >> HHIP

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296575
Start	144659765:144659765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780145807
CDS Mutation	c.758T>C
AA Mutation	p.Ile253Thr(p.I253T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296575
Start	144646712:144646712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.37G>C
AA Mutation	p.Ala13Pro(p.A13P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000296575
Start	144714297:144714297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1496G>A
AA Mutation	p.Gly499Asp(p.G499D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000296575
Start	144652725:144652725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773363775
CDS Mutation	c.400G>T
AA Mutation	p.Asp134Tyr(p.D134Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000296575
Start	144708262:144708262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1252A>G
AA Mutation	p.Thr418Ala(p.T418A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000296575
Start	144715416:144715416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1664G>A
AA Mutation	p.Gly555Glu(p.G555E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000296575
Start	144708206:144708206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1196C>G
AA Mutation	p.Thr399Arg(p.T399R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000296575
Start	144715374:144715374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1622G>T
AA Mutation	p.Gly541Val(p.G541V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000296575
Start	144737926:144737926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2072A>G
AA Mutation	p.Tyr691Cys(p.Y691C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000296575
Start	144646940:144646940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.265C>T
AA Mutation	p.Arg89Cys(p.R89C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296575
Start	144708219:144708219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144126673
CDS Mutation	c.1209C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296575
Start	144734840:144734840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748140286
CDS Mutation	c.1860G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296575
Start	144646930:144646930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202159669
CDS Mutation	c.255G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296575
Start	144646900:144646900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201201764
CDS Mutation	c.225G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296575
Start	144646879:144646879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.204G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296575
Start	144737826:144737826(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1977delA
AA Mutation	p.Gly660AspfsTer17(p.G660Dfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296575
Start	144706582:144706582(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.887delA
AA Mutation	p.Asn296MetfsTer41(p.N296Mfs*41)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000296575
Start	144707087:144707087(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.989delA
AA Mutation	p.Asn330IlefsTer7(p.N330Ifs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296575
Start	144734833:144734833(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1857delC
AA Mutation	p.Thr620ArgfsTer57(p.T620Rfs*57)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296575
Start	144646803:144646804(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.134dupC
AA Mutation	p.Lys46GlufsTer38(p.K46Efs*38)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296575
Start	144646750:144646751(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.79dupG
AA Mutation	p.Glu27GlyfsTer57(p.E27Gfs*57)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	22
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000296575
Start	144708166:144708166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1158-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript