Mutation

Primary Site >> Liver Cancer

Gene >> ATR

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000350721
Start	142553289:142553289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2743G>A
AA Mutation	p.Val915Ile(p.V915I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000350721
Start	142513601:142513601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4541G>T
AA Mutation	p.Cys1514Phe(p.C1514F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000350721
Start	142535120:142535120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3905A>T
AA Mutation	p.His1302Leu(p.H1302L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000350721
Start	142562349:142562349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1053G>T
AA Mutation	p.Gln351His(p.Q351H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000350721
Start	142496474:142496474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5785A>T
AA Mutation	p.Arg1929Trp(p.R1929W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000350721
Start	142559409:142559409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1574A>T
AA Mutation	p.Lys525Met(p.K525M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000350721
Start	142469523:142469523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6366A>G
AA Mutation	p.Ile2122Met(p.I2122M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000350721
Start	142549591:142549591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3059A>T
AA Mutation	p.Gln1020Leu(p.Q1020L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000350721
Start	142556391:142556391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2070G>C
AA Mutation	p.Lys690Asn(p.K690N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000350721
Start	142560389:142560389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752635785
CDS Mutation	c.1415C>G
AA Mutation	p.Ser472Cys(p.S472C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350721
Start	142469493:142469493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774455552
CDS Mutation	c.6396T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350721
Start	142556409:142556409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2052T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350721
Start	142497144:142497144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5607G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350721
Start	142469397:142469397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6492A>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000350721
Start	142470154:142470155(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.6250dupT
AA Mutation	p.Tyr2084LeufsTer13(p.Y2084Lfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	16
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000350721
Start	142498775:142498775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5381-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	17
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000350721
Start	142559250:142559250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1732+1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript