Cell Line Synopsis
Cell Line Overview
Mutations
Copy Number Variation
Gene Expression
RNAi
Compound Sensitivity Profile
Similar Cell Lines

NCI-H1395 - Mutations - Cell Line Synopsis



    


COSMIC - Cell Lines Project

29 mutations reported
7 synonymous mutations reported
Filter:
External Data Sources: Catalogue of Somatic Mutations in Cancer
Gene Name(s) Gene Transcript AA Syntax CDS Syntax Mutation Type Pubmed ID
ENST00000316490p.?c.9833-9A>GUnknown
NM_018695.1p.Q1237Pc.3710A>CSubstitution - Missense
KRTAP5-10ENSG00000204572ENST00000398531p.S7Ac.19T>GSubstitution - Missense
KRTAP5-10ENSG00000204572ENST00000376536p.S7Ac.19T>GSubstitution - Missense
ENST00000416172_v68p.P258Ac.772C>GSubstitution - Missense
NPAS1ENSG00000130751ENST00000449844p.E297Dc.891G>CSubstitution - Missense
ERBB2IPENSG00000112851ENST00000380943p.Q1237Pc.3710A>CSubstitution - Missense
ERBB2IPENSG00000112851ENST00000284037p.Q1278Pc.3833A>CSubstitution - Missense
NM_001007157.1p.T152Pc.454A>CSubstitution - Missense
DENND4AENSG00000174485ENST00000443035p.P701Sc.2101C>TSubstitution - Missense
PRB1ENSG00000251655ENST00000500254p.S28Cc.83C>GSubstitution - Missense
TOR1AIP1ENSG00000143337ENST00000435319p.P64Qc.191C>ASubstitution - Missense
CLCA4ENSG00000016602ENST00000263723p.H61Yc.181C>TSubstitution - Missense
HNRNPKENSG00000165119ENST00000376264p.A67Vc.200C>TSubstitution - Missense
MUC16ENSG00000181143ENST00000380951p.P306Pc.918A>GSubstitution - coding silent
PHF14ENSG00000106443ENST00000403050p.T152Pc.454A>CSubstitution - Missense
MUC16ENSG00000181143ENST00000397910p.P13621Pc.40863A>GSubstitution - coding silent
HNRNPKENSG00000165119ENST00000376264p.A67Ac.201T>CSubstitution - coding silent
C22orf15ENSG00000169314ENST00000402217p.R74Gc.220C>GSubstitution - Missense
ZNF609ENSG00000180357ENST00000416172p.P258Ac.772C>GSubstitution - Missense
SPATA2LENSG00000158792ENST00000289805p.Q408Kc.1222C>ASubstitution - Missense
CLCA4ENSG00000016602ENST00000370563p.H348Yc.1042C>TSubstitution - Missense
GRAMD1AENSG00000089351ENST00000317991p.R139Hc.416G>ASubstitution - Missense
DENND4AENSG00000174485ENST00000431932p.P701Sc.2101C>TSubstitution - Missense
LRRC49ENSG00000137821ENST00000260382p.L162Lc.484C>TSubstitution - coding silent
SLC25A1ENSG00000100075ENST00000215882p.T185Pc.553A>CSubstitution - Missense
HNRNPKENSG00000165119ENST00000376281p.A67Ac.201T>CSubstitution - coding silent
HNRNPKENSG00000165119ENST00000376281p.A67Vc.200C>TSubstitution - Missense
ENST00000316490_v65p.?c.9977-9A>GUnknown


COSMIC

57 mutations reported
8 synonymous mutations reported
Filter:
External Data Sources: Catalogue of Somatic Mutations in Cancer
Gene Name(s) Gene Transcript AA Syntax CDS Syntax Mutation Type Pubmed ID
GHRENSG00000112964ENST00000230882p.V343Ic.1027G>ASubstitution - Missense
STK11ENSG00000118046ENST00000326873p.E57fs*7c.169delGDeletion - Frameshift
STK11ENSG00000118046ENST00000326873p.E57fs*7c.169delGDeletion - Frameshift
ERN1ENSG00000178607ENST00000433197p.L474Rc.1421T>GSubstitution - Missense
ERN1ENSG00000178607ENST00000433197p.L474Rc.1421T>GSubstitution - Missense
SOS1ENSG00000115904ENST00000426016p.Y1031fs*1c.3092_3093insAInsertion - Frameshift
GPC3ENSG00000147257ENST00000370818p.D164Hc.490G>CSubstitution - Missense
SOS1ENSG00000115904ENST00000426016p.Y1031fs*1c.3092_3093insAInsertion - Frameshift
XM_372532.2p.E273*c.817G>TSubstitution - Nonsense
ERN1ENSG00000178607ENST00000433197p.L474Rc.1421T>GSubstitution - Missense16140923
ERN1ENSG00000178607ENST00000433197p.L474Rc.1421T>GSubstitution - Missense16140923
FBXO25ENSG00000147364ENST00000276326p.S190Sc.570T>ASubstitution - coding silent
STK11ENSG00000118046ENST00000326873p.E57fs*7c.169delGDeletion - Frameshift16140923
STK11ENSG00000118046ENST00000326873p.E57fs*7c.169delGDeletion - Frameshift16140923
AXLENSG00000167601ENST00000359092p.A181Ac.543C>TSubstitution - coding silent16140923
AXLENSG00000167601ENST00000359092p.A181Ac.543C>TSubstitution - coding silent16140923
RGAG1ENSG00000243978ENST00000465301p.S382Sc.1146T>CSubstitution - coding silent
GPC3ENSG00000147257ENST00000370818p.D164Hc.490G>CSubstitution - Missense
BIRC6ENSG00000115760ENST00000421745p.T371Sc.1111A>TSubstitution - Missense
DDX23ENSG00000174243ENST00000308025p.R73Wc.217C>TSubstitution - Missense
NM_001010888.1p.E647Dc.1941G>TSubstitution - Missense
NLRP1ENSG00000091592ENST00000572272p.K270*c.808A>TSubstitution - Nonsense
HMGN5ENSG00000198157ENST00000358130p.E258*c.772G>TSubstitution - Nonsense
PDCD5ENSG00000105185ENST00000221784p.R55Sc.165G>TSubstitution - Missense
ATMENSG00000149311ENST00000278616p.T2666Ac.7996A>GSubstitution - Missense
ATMENSG00000149311ENST00000278616p.T2666Ac.7996A>GSubstitution - Missense
ATMENSG00000149311ENST00000278616p.T2666Ac.7996A>GSubstitution - Missense16140923
ATMENSG00000149311ENST00000278616p.T2666Ac.7996A>GSubstitution - Missense16140923
NM_138995p.S867*c.2600C>ASubstitution - Nonsense16140923
NM_138995p.S867*c.2600C>ASubstitution - Nonsense16140923
NM_015057.1p.G1204Lc.3610_3610GG>TTSubstitution - Missense
PPARGC1AENSG00000109819ENST00000264867p.Q431Hc.1293G>CSubstitution - Missense
NLRP4ENSG00000160505ENST00000301295p.W111Lc.332G>TSubstitution - Missense
CENPCENSG00000145241ENST00000273853p.V827Lc.2479G>TSubstitution - Missense
CENPCENSG00000145241ENST00000273853p.V827Lc.2479G>TSubstitution - Missense
GNB5ENSG00000069966ENST00000261837p.A200Sc.598G>TSubstitution - Missense
IMPDH2ENSG00000178035ENST00000326739p.D226Hc.676G>CSubstitution - Missense
IMPDH2ENSG00000178035ENST00000326739p.D226Hc.676G>CSubstitution - Missense
BRAFENSG00000157764ENST00000288602p.G469Ac.1406G>CSubstitution - Missense12068308
BRAFENSG00000157764ENST00000288602p.G469Ac.1406G>CSubstitution - Missense
BRAFENSG00000157764ENST00000288602p.G469Ac.1406G>CSubstitution - Missense16140923
BRAFENSG00000157764ENST00000288602p.G469Ac.1406G>CSubstitution - Missense16140923
NLRP1ENSG00000091592ENST00000572272p.K655*c.1963A>TSubstitution - Nonsense
KAT7ENSG00000136504ENST00000259021p.G505Sc.1513G>ASubstitution - Missense
ADRA2BENSG00000222040ENST00000409345p.P147Pc.441C>ASubstitution - coding silent
SMURF2ENSG00000108854ENST00000262435p.R592*c.1774C>TSubstitution - Nonsense
TRIM36ENSG00000152503ENST00000282369p.S447Cc.1339A>TSubstitution - Missense
PROM1ENSG00000007062ENST00000447510p.A179Lc.535_536GC>TTSubstitution - Missense
CXCR2ENSG00000180871ENST00000318507p.G354Wc.1060G>TSubstitution - Missense
ENST00000221482p.G1052Vc.3155G>TSubstitution - Missense
ALDH1A3ENSG00000184254ENST00000329841p.V202Vc.606C>ASubstitution - coding silent
NM_133170.2p.Q479Ec.1435C>GSubstitution - Missense
NUP214ENSG00000126883ENST00000359428p.E1580*c.4738G>TSubstitution - Nonsense
ATF7IPENSG00000171681ENST00000261168p.A1242Ac.3726A>CSubstitution - coding silent
LRR1ENSG00000165501ENST00000298288p.R172Lc.515G>TSubstitution - Missense
ITPR3ENSG00000096433ENST00000374316p.L634Lc.1902C>TSubstitution - coding silent
BRAFENSG00000157764ENST00000288602p.G469Ac.1406G>CSubstitution - Missense19010912