Mutation

Primary Site >> Stomach Cancer

Gene >> XAB2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358368
Start	7619615:7619615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs538580383
CDS Mutation	c.2539G>A
AA Mutation	p.Ala847Thr(p.A847T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358368
Start	7624340:7624340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.928A>G
AA Mutation	p.Lys310Glu(p.K310E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358368
Start	7628223:7628223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.127G>A
AA Mutation	p.Glu43Lys(p.E43K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358368
Start	7622640:7622640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753191949
CDS Mutation	c.1393C>T
AA Mutation	p.Arg465Cys(p.R465C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000358368
Start	7628251:7628251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.99C>A
AA Mutation	p.Phe33Leu(p.F33L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000358368
Start	7625966:7625966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.736G>A
AA Mutation	p.Gly246Arg(p.G246R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000358368
Start	7627798:7627798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.254G>A
AA Mutation	p.Arg85His(p.R85H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000358368
Start	7625986:7625986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.716A>G
AA Mutation	p.Asn239Ser(p.N239S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000358368
Start	7620549:7620549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746259500
CDS Mutation	c.2092C>T
AA Mutation	p.Arg698Trp(p.R698W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000358368
Start	7627391:7627391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780029774
CDS Mutation	c.374G>A
AA Mutation	p.Arg125His(p.R125H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000358368
Start	7619973:7619973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2369G>A
AA Mutation	p.Arg790His(p.R790H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000358368
Start	7620313:7620313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2228C>T
AA Mutation	p.Ser743Leu(p.S743L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000358368
Start	7622426:7622426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772361220
CDS Mutation	c.1522G>A
AA Mutation	p.Asp508Asn(p.D508N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358368
Start	7623188:7623188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1221C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358368
Start	7626154:7626154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.639C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358368
Start	7622346:7622346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774698695
CDS Mutation	c.1602C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358368
Start	7624362:7624362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201776166
CDS Mutation	c.906C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358368
Start	7627294:7627294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.471C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358368
Start	7625964:7625964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770253298
CDS Mutation	c.738G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358368
Start	7622608:7622608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774152276
CDS Mutation	c.1425C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000358368
Start	7627266:7627266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.499C>T
AA Mutation	p.Arg167Ter(p.R167*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000358368
Start	7620670:7620670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1972-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript