Mutation

Primary Site >> Stomach Cancer

Gene >> XK

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378616
Start	37727798:37727798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.671T>C
AA Mutation	p.Val224Ala(p.V224A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378616
Start	37727683:37727683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367651585
CDS Mutation	c.556C>T
AA Mutation	p.Arg186Cys(p.R186C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000378616
Start	37694437:37694437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.397C>G
AA Mutation	p.Arg133Gly(p.R133G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000378616
Start	37727690:37727690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.563A>C
AA Mutation	p.Asn188Thr(p.N188T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000378616
Start	37686133:37686133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.172G>A
AA Mutation	p.Val58Ile(p.V58I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000378616
Start	37727690:37727690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.563A>G
AA Mutation	p.Asn188Ser(p.N188S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000378616
Start	37694456:37694456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.416C>T
AA Mutation	p.Ala139Val(p.A139V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000378616
Start	37727738:37727738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.611A>C
AA Mutation	p.Lys204Thr(p.K204T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378616
Start	37728168:37728168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368546529
CDS Mutation	c.1041C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378616
Start	37686117:37686117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.156G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000378616
Start	37728332:37728332(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1209delA
AA Mutation	p.Lys403AsnfsTer6(p.K403Nfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000378616
Start	37728331:37728332(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1209dupA
AA Mutation	p.Pro404ThrfsTer3(p.P404Tfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript