ID   GM14660
AC   CVCL_7611
SY   GM17031; GM17188
DR   CLO; CLO_0013777
DR   CLO; CLO_0014727
DR   CLO; CLO_0031640
DR   Coriell; GM14660
DR   Coriell; GM17031
DR   Coriell; GM17188
DR   GEO; GSM273442
DR   GEO; GSM569710
DR   GEO; GSM596252
DR   GEO; GSM597047
DR   GEO; GSM924698
DR   IPD-IMGT/HLA; 19230
DR   Wikidata; Q54847367
RX   PubMed=11416159;
CC   Part of: Human variation panel.
CC   Population: African American.
CC   HLA typing: A*23:DFKR,34:02; B*49:01,53:01; C*06:02,07:CVAG; DRB1*12:CVT,15:03 (IPD-IMGT/HLA=19230).
CC   Sequence variation: Mutation; HGNC; 2625; CYP2D6; Simple; p.Thr107Ile (c.320C>T); ClinVar=VCV000039379; Zygosity=Heterozygous; Note=CYP2D6*17 allele (Coriell=GM17188).
CC   Sequence variation: Mutation; HGNC; 2625; CYP2D6; Simple; p.Arg296Cys (c.886C>T); ClinVar=VCV000242771; Zygosity=Heterozygous; Note=CYP2D6*17 allele (Coriell=GM17188).
CC   Sequence variation: Mutation; HGNC; 2625; CYP2D6; Simple; p.Ser486Thr (c.1457G>C); ClinVar=VCV000242701; Zygosity=Heterozygous; Note=CYP2D6*17 allele (Coriell=GM17188).
CC   Transformant: NCBI_TaxID; 10376; Epstein-Barr virus (EBV).
CC   Omics: DNA methylation analysis.
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
ST   Source(s): PubMed=11416159
ST   Amelogenin: X
ST   D18S51: 14,15
ST   D21S11: 31,35
ST   D8S1179: 14,15
ST   FGA: 22,24
ST   TH01: 7,9
ST   vWA: 15,18
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   26Y
CA   Transformed cell line
DT   Created: 04-04-12; Last updated: 30-01-24; Version: 22
//
RX   PubMed=11416159; DOI=10.1073/pnas.121616198;
RA   Masters J.R.W., Thomson J.A., Daly-Burns B., Reid Y.A., Dirks W.G.,
RA   Packer P., Toji L.H., Ohno T., Tanabe H., Arlett C.F., Kelland L.R.,
RA   Harrison M., Virmani A.K., Ward T.H., Ayres K.L., Debenham P.G.;
RT   "Short tandem repeat profiling provides an international reference
RT   standard for human cell lines.";
RL   Proc. Natl. Acad. Sci. U.S.A. 98:8012-8017(2001).
//