Mutation

Primary Site >> Stomach Cancer

Gene >> CD6

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313421
Start	61008786:61008786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.722C>T
AA Mutation	p.Pro241Leu(p.P241L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000313421
Start	61009629:61009629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.839T>A
AA Mutation	p.Val280Glu(p.V280E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000313421
Start	61018351:61018351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1900C>T
AA Mutation	p.Pro634Ser(p.P634S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000313421
Start	61015725:61015725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1400C>A
AA Mutation	p.Pro467His(p.P467H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000313421
Start	61018010:61018010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1834T>G
AA Mutation	p.Ser612Ala(p.S612A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000313421
Start	61015770:61015770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763287629
CDS Mutation	c.1445C>T
AA Mutation	p.Ser482Leu(p.S482L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000313421
Start	61013928:61013928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1301T>C
AA Mutation	p.Val434Ala(p.V434A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313421
Start	61015786:61015786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs538627375
CDS Mutation	c.1461G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313421
Start	61018386:61018386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1935C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313421
Start	61018389:61018389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532885642
CDS Mutation	c.1938T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000313421
Start	61008778:61008796(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.718_736delTGCCCGGGGCTGCCAGGAC
AA Mutation	p.Cys240SerfsTer22(p.C240Sfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000313421
Start	61008607:61008608(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.544dupT
AA Mutation	p.Trp182LeufsTer7(p.W182Lfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000313421
Start	61009654:61009655(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.870_871dupTG
AA Mutation	p.Asp291ValfsTer94(p.D291Vfs*94)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	14
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000313421
Start	61008532:61008532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.470-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript