Mutation

Primary Site >> Stomach Cancer

Gene >> AEBP1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000223357
Start	44112889:44112889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2549A>G
AA Mutation	p.Lys850Arg(p.K850R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000223357
Start	44113827:44113827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3043C>A
AA Mutation	p.Gln1015Lys(p.Q1015K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000223357
Start	44110729:44110729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150909656
CDS Mutation	c.1405G>A
AA Mutation	p.Asp469Asn(p.D469N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000223357
Start	44104735:44104735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.70C>T
AA Mutation	p.Arg24Cys(p.R24C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000223357
Start	44113615:44113615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2831G>A
AA Mutation	p.Arg944Gln(p.R944Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000223357
Start	44107632:44107632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.671C>T
AA Mutation	p.Pro224Leu(p.P224L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000223357
Start	44110295:44110295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1349G>A
AA Mutation	p.Arg450Lys(p.R450K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000223357
Start	44110089:44110089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749154733
CDS Mutation	c.1225G>A
AA Mutation	p.Gly409Ser(p.G409S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000223357
Start	44110786:44110786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1462T>C
AA Mutation	p.Tyr488His(p.Y488H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000223357
Start	44112780:44112780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2440T>C
AA Mutation	p.Trp814Arg(p.W814R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000223357
Start	44107502:44107502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.659A>G
AA Mutation	p.His220Arg(p.H220R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000223357
Start	44110241:44110241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757009902
CDS Mutation	c.1295C>T
AA Mutation	p.Ala432Val(p.A432V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000223357
Start	44113702:44113702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2918T>C
AA Mutation	p.Ile973Thr(p.I973T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000223357
Start	44113783:44113783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2999G>A
AA Mutation	p.Arg1000Gln(p.R1000Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000223357
Start	44109144:44109144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1056G>T
AA Mutation	p.Glu352Asp(p.E352D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000223357
Start	44107671:44107671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.710A>G
AA Mutation	p.Asp237Gly(p.D237G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223357
Start	44110927:44110927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201501212
CDS Mutation	c.1500C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223357
Start	44111188:44111188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1665G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223357
Start	44113901:44113901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749382269
CDS Mutation	c.3117C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223357
Start	44112201:44112201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2097T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223357
Start	44110749:44110749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778106615
CDS Mutation	c.1425C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223357
Start	44110242:44110242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372850520
CDS Mutation	c.1296G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223357
Start	44111921:44111921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1908G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000223357
Start	44107633:44107633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758385259
CDS Mutation	c.672G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000223357
Start	44104832:44104832(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.170delC
AA Mutation	p.Pro57ArgfsTer235(p.P57Rfs*235)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000223357
Start	44106848:44106848(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.561delC
AA Mutation	p.Ser188AlafsTer104(p.S188Afs*104)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000223357
Start	44104864:44104864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.199C>T
AA Mutation	p.Arg67Ter(p.R67*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript