Mutation

Primary Site >> Liver Cancer

Gene >> PREX2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000288368
Start	68108167:68108167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2774T>A
AA Mutation	p.Ile925Asn(p.I925N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000288368
Start	68099711:68099711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2583G>T
AA Mutation	p.Glu861Asp(p.E861D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000288368
Start	68231347:68231347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4790G>T
AA Mutation	p.Cys1597Phe(p.C1597F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000288368
Start	68108134:68108134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2741C>T
AA Mutation	p.Ala914Val(p.A914V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000288368
Start	68118559:68118559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3336C>A
AA Mutation	p.Asn1112Lys(p.N1112K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000288368
Start	68119494:68119494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3484C>A
AA Mutation	p.Leu1162Ile(p.L1162I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000288368
Start	68022060:68022060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.361G>C
AA Mutation	p.Glu121Gln(p.E121Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000288368
Start	68090609:68090609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2144C>T
AA Mutation	p.Pro715Leu(p.P715L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000288368
Start	68192416:68192416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4495G>A
AA Mutation	p.Ala1499Thr(p.A1499T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000288368
Start	68109540:68109540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3063A>T
AA Mutation	p.Glu1021Asp(p.E1021D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000288368
Start	68191774:68191774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4399G>T
AA Mutation	p.Ala1467Ser(p.A1467S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000288368
Start	68120224:68120224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3533G>C
AA Mutation	p.Gly1178Ala(p.G1178A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000288368
Start	68053241:68053241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751712561
CDS Mutation	c.1088G>A
AA Mutation	p.Arg363Gln(p.R363Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000288368
Start	68053201:68053201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1048C>A
AA Mutation	p.His350Asn(p.H350N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000288368
Start	68192455:68192455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4534T>C
AA Mutation	p.Ser1512Pro(p.S1512P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000288368
Start	68120248:68120248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3557A>G
AA Mutation	p.Asp1186Gly(p.D1186G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000288368
Start	68134194:68134194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3902G>C
AA Mutation	p.Trp1301Ser(p.W1301S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000288368
Start	68109620:68109620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3143A>T
AA Mutation	p.Asp1048Val(p.D1048V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000288368
Start	68055957:68055957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1221T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000288368
Start	68038173:68038173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.720T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000288368
Start	67952529:67952529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.135G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000288368
Start	68108228:68108228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2835T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000288368
Start	68053116:68053116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.963A>G
Mutation Classification	Silent
Feature Type	Transcript