Mutation

Primary Site >> Stomach Cancer

Gene >> CENPE

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265148
Start	103144567:103144567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4909A>G
AA Mutation	p.Asn1637Asp(p.N1637D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265148
Start	103116665:103116665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7354C>T
AA Mutation	p.Pro2452Ser(p.P2452S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265148
Start	103159035:103159035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2576C>T
AA Mutation	p.Ser859Leu(p.S859L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265148
Start	103160746:103160746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2165T>G
AA Mutation	p.Ile722Ser(p.I722S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265148
Start	103195209:103195209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.382C>T
AA Mutation	p.Arg128Cys(p.R128C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000265148
Start	103196250:103196250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.151C>T
AA Mutation	p.Arg51Cys(p.R51C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265148
Start	103159183:103159183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2428T>C
AA Mutation	p.Ser810Pro(p.S810P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265148
Start	103180442:103180442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1111A>G
AA Mutation	p.Met371Val(p.M371V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000265148
Start	103145848:103145848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4394T>C
AA Mutation	p.Ile1465Thr(p.I1465T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000265148
Start	103144531:103144531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4945T>A
AA Mutation	p.Leu1649Met(p.L1649M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000265148
Start	103144575:103144575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4901C>T
AA Mutation	p.Thr1634Ile(p.T1634I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000265148
Start	103195226:103195226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.365A>C
AA Mutation	p.Asp122Ala(p.D122A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000265148
Start	103145286:103145286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4621A>G
AA Mutation	p.Ser1541Gly(p.S1541G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000265148
Start	103158860:103158860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2628G>T
AA Mutation	p.Gln876His(p.Q876H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000265148
Start	103146010:103146010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4232C>A
AA Mutation	p.Pro1411His(p.P1411H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265148
Start	103158773:103158773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2715T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265148
Start	103182840:103182840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.885C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265148
Start	103138429:103138429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6225A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265148
Start	103185820:103185820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.735A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265148
Start	103133752:103133752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6663A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265148
Start	103180365:103180365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1188C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265148
Start	103145901:103145901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs114566933
CDS Mutation	c.4341A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265148
Start	103108888:103108888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7926T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265148
Start	103183221:103183221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.813A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265148
Start	103108879:103108879(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.7935delT
AA Mutation	p.Phe2645LeufsTer22(p.F2645Lfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000265148
Start	103145253:103145253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4654C>T
AA Mutation	p.Gln1552Ter(p.Q1552*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265148
Start	103148898:103148899(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3788_3789insAAATACTTACCCAG
AA Mutation	p.Gln1264AsnfsTer7(p.Q1264Nfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript