Mutation

Primary Site >> Stomach Cancer

Gene >> EYA1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340726
Start	71211252:71211252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1602A>C
AA Mutation	p.Lys534Asn(p.K534N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340726
Start	71211223:71211223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1631G>T
AA Mutation	p.Arg544Met(p.R544M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000340726
Start	71334107:71334107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.192C>A
AA Mutation	p.Phe64Leu(p.F64L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000340726
Start	71322257:71322257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.214A>G
AA Mutation	p.Ser72Gly(p.S72G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000340726
Start	71299709:71299709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.568A>G
AA Mutation	p.Thr190Ala(p.T190A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000340726
Start	71271838:71271838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142104253
CDS Mutation	c.886C>T
AA Mutation	p.Arg296Cys(p.R296C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000340726
Start	71211222:71211222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1632G>T
AA Mutation	p.Arg544Ser(p.R544S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000340726
Start	71354889:71354889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.17T>C
AA Mutation	p.Leu6Pro(p.L6P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000340726
Start	71215498:71215498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1486G>A
AA Mutation	p.Val496Met(p.V496M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000340726
Start	71317584:71317584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.524C>A
AA Mutation	p.Pro175His(p.P175H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000340726
Start	71299089:71299089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.784C>T
AA Mutation	p.Pro262Ser(p.P262S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000340726
Start	71215703:71215703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1386A>C
AA Mutation	p.Glu462Asp(p.E462D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340726
Start	71215643:71215643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1446C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340726
Start	71215694:71215694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1395G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340726
Start	71317613:71317613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.495C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340726
Start	71299090:71299090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146648560
CDS Mutation	c.783G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340726
Start	71216744:71216744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1308C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340726
Start	71211213:71211213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1641A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000340726
Start	71211157:71211157(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1697delA
AA Mutation	p.Lys566SerfsTer73(p.K566Sfs*73)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000340726
Start	71244615:71244615(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1128delT
AA Mutation	p.Phe376LeufsTer4(p.F376Lfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000340726
Start	71271873:71271873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.851C>A
AA Mutation	p.Ser284Ter(p.S284*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000340726
Start	71199421:71199421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1699-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript