Mutation

Primary Site >> Stomach Cancer

Gene >> ATP2B4

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357681
Start	203721338:203721338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2740C>T
AA Mutation	p.Arg914Cys(p.R914C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357681
Start	203713217:203713217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2264G>A
AA Mutation	p.Arg755Gln(p.R755Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000357681
Start	203700852:203700852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.830A>C
AA Mutation	p.Asn277Thr(p.N277T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000357681
Start	203727506:203727506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3244G>A
AA Mutation	p.Ala1082Thr(p.A1082T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000357681
Start	203703711:203703711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200430665
CDS Mutation	c.997G>A
AA Mutation	p.Asp333Asn(p.D333N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000357681
Start	203699525:203699525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.457G>A
AA Mutation	p.Ala153Thr(p.A153T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000357681
Start	203708010:203708010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199754074
CDS Mutation	c.1463G>A
AA Mutation	p.Arg488His(p.R488H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000357681
Start	203727495:203727495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3233A>T
AA Mutation	p.Glu1078Val(p.E1078V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000357681
Start	203723945:203723945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3089T>C
AA Mutation	p.Leu1030Pro(p.L1030P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000357681
Start	203700854:203700854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.832T>C
AA Mutation	p.Ser278Pro(p.S278P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000357681
Start	203711991:203711991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2063C>A
AA Mutation	p.Ala688Asp(p.A688D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357681
Start	203722548:203722548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2883C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357681
Start	203703665:203703665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145839216
CDS Mutation	c.951C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357681
Start	203714238:203714238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746454064
CDS Mutation	c.2367C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357681
Start	203707927:203707927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762715419
CDS Mutation	c.1380C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357681
Start	203711012:203711012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs181836521
CDS Mutation	c.1935C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000357681
Start	203698218:203698218(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.261delC
AA Mutation	p.Lys89SerfsTer6(p.K89Sfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000357681
Start	203699559:203699559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.491T>A
AA Mutation	p.Leu164Ter(p.L164*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000357681
Start	203721277:203721278(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2684dupC
AA Mutation	p.Thr896TyrfsTer14(p.T896Yfs*14)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript