ID   Hs 936.T(C1)
AC   CVCL_1034
DR   CLO; CLO_0004241
DR   ATCC; CRL-7687
DR   cancercelllines; CVCL_1034
DR   Wikidata; Q54896243
CC   Part of: Naval Biosciences Laboratory (NBL) collection (transferred to ATCC in 1982).
CC   Population: Caucasian.
CC   Sequence variation: Mutation; HGNC; HGNC:7989; NRAS; Simple; p.Gln61Lys (c.181C>A); ClinVar=VCV000073058; Zygosity=Heterozygous (from parent cell line).
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
ST   Source(s): ATCC=CRL-7687
ST   Amelogenin: X,Y
ST   CSF1PO: 8,12
ST   D13S317: 8
ST   D16S539: 9,12
ST   D18S51: 17,18
ST   D19S433: 14.2
ST   D21S11: 29,30
ST   D2S1338: 17,21
ST   D3S1358: 15,18
ST   D5S818: 9,12
ST   D7S820: 8,11
ST   D8S1179: 11,16
ST   FGA: 21,22
ST   Penta D: 10
ST   Penta E: 12,18
ST   TH01: 7,9.3
ST   TPOX: 8
ST   vWA: 17,18
DI   NCIt; C3224; Melanoma
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_1033 ! Hs 936.T
SX   Male
AG   Age unspecified
CA   Cancer cell line
DT   Created: 04-04-12; Last updated: 19-12-24; Version: 16
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