Mutation

Primary Site >> Stomach Cancer

Gene >> COPA

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000241704
Start	160297372:160297372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138441444
CDS Mutation	c.2234G>A
AA Mutation	p.Arg745His(p.R745H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000241704
Start	160340250:160340250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.85C>T
AA Mutation	p.His29Tyr(p.H29Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000241704
Start	160305515:160305515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767740500
CDS Mutation	c.1585C>T
AA Mutation	p.Arg529Cys(p.R529C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000241704
Start	160299112:160299112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1820A>C
AA Mutation	p.Lys607Thr(p.K607T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000241704
Start	160297373:160297373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763748181
CDS Mutation	c.2233C>T
AA Mutation	p.Arg745Cys(p.R745C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000241704
Start	160297362:160297362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2244C>G
AA Mutation	p.Ile748Met(p.I748M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000241704
Start	160297666:160297666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2057A>G
AA Mutation	p.Asn686Ser(p.N686S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000241704
Start	160298912:160298912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1910T>C
AA Mutation	p.Val637Ala(p.V637A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000241704
Start	160307173:160307173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199634303
CDS Mutation	c.1292G>A
AA Mutation	p.Arg431Gln(p.R431Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000241704
Start	160291376:160291376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749061726
CDS Mutation	c.3379C>T
AA Mutation	p.Arg1127Cys(p.R1127C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241704
Start	160323525:160323525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.612C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241704
Start	160291371:160291371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3384A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241704
Start	160294817:160294817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2517T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241704
Start	160292603:160292603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2841A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241704
Start	160291401:160291401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3354C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000241704
Start	160290677:160290677(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3430delA
AA Mutation	p.Ile1144SerfsTer39(p.I1144Sfs*39)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000241704
Start	160295758:160295758(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2454delT
AA Mutation	p.Phe818LeufsTer65(p.F818Lfs*65)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000241704
Start	160297696:160297696(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2027delA
AA Mutation	p.Lys676SerfsTer38(p.K676Sfs*38)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000241704
Start	160325637:160325637(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.512delA
AA Mutation	p.Asn171ThrfsTer11(p.N171Tfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000241704
Start	160325636:160325637(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.512dupA
AA Mutation	p.Asn171LysfsTer18(p.N171Kfs*18)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000241704
Start	160291427:160291428(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3326_3327dupTC
AA Mutation	p.Asn1110SerfsTer21(p.N1110Sfs*21)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript