Mutation

Primary Site >> Stomach Cancer

Gene >> ICK

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000350082
Start	53013713:53013713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs75380402
CDS Mutation	c.1101C>A
AA Mutation	p.Asp367Glu(p.D367E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000350082
Start	53032555:53032555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.256C>A
AA Mutation	p.Leu86Ile(p.L86I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000350082
Start	53005216:53005216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1832G>A
AA Mutation	p.Arg611Gln(p.R611Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000350082
Start	53011877:53011877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757793482
CDS Mutation	c.1384G>T
AA Mutation	p.Gly462Cys(p.G462C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000350082
Start	53018439:53018439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.554C>T
AA Mutation	p.Ala185Val(p.A185V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000350082
Start	53041169:53041169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752216774
CDS Mutation	c.68G>A
AA Mutation	p.Ser23Asn(p.S23N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000350082
Start	53019275:53019275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778947062
CDS Mutation	c.443G>A
AA Mutation	p.Arg148Gln(p.R148Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350082
Start	53041150:53041150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.87G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350082
Start	53006367:53006367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752631250
CDS Mutation	c.1692C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350082
Start	53032574:53032574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754954751
CDS Mutation	c.237C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350082
Start	53005179:53005179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1869C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000350082
Start	53013783:53013783(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1031delC
AA Mutation	p.Pro344LeufsTer54(p.P344Lfs*54)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	13
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000350082
Start	53013826:53013827(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.987_988insGAAGAGGAATAAA
AA Mutation	p.His330GlufsTer4(p.H330Efs*4)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript