Mutation

Primary Site >> Stomach Cancer

Gene >> CCDC151

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356392
Start	11434813:11434813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.204C>A
AA Mutation	p.His68Gln(p.H68Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356392
Start	11424023:11424023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748442231
CDS Mutation	c.970C>T
AA Mutation	p.Arg324Cys(p.R324C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356392
Start	11430724:11430724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.419C>A
AA Mutation	p.Pro140Gln(p.P140Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356392
Start	11426212:11426212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747108388
CDS Mutation	c.895C>T
AA Mutation	p.Arg299Cys(p.R299C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356392
Start	11426989:11426989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.496G>A
AA Mutation	p.Ala166Thr(p.A166T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000356392
Start	11420851:11420851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1772G>A
AA Mutation	p.Arg591His(p.R591H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000356392
Start	11426777:11426777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs529248956
CDS Mutation	c.620G>A
AA Mutation	p.Arg207Gln(p.R207Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000356392
Start	11434798:11434798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.219G>T
AA Mutation	p.Glu73Asp(p.E73D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000356392
Start	11420923:11420923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1700A>G
AA Mutation	p.Asn567Ser(p.N567S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356392
Start	11420838:11420838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1785C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356392
Start	11420847:11420847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1776T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356392
Start	11430998:11430998(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.267delT
AA Mutation	p.Phe89LeufsTer27(p.F89Lfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000356392
Start	11426233:11426233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.874C>T
AA Mutation	p.Arg292Ter(p.R292*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript