SPOCK1 c.187-30594C>T

Variant ID: 5-136633338-G-A

NM_004598.3(SPOCK1):c.187-30594C>T

This variant was identified in 10 publications

View GRCh38 version.




Publications:


Sequencing of human identification markers in an Uyghur population using the MiSeq FGxTM Forensic Genomics System.

Forensic Sciences Research
Simayijiang, Halimureti H; Morling, Niels N; Børsting, Claus C
Publication Date: 2022

Variant appearance in text: rs13182883
PubMed Link: 35784409
Variant Present in the following documents:
  • Main text
  • TFSR_7_1779967.pdf
View BVdb publication page



Response prediction in patients with gastric and esophagogastric adenocarcinoma under neoadjuvant chemotherapy using targeted gene expression analysis and next-generation sequencing in pre-therapeutic biopsies.

Journal Of Cancer Research And Clinical Oncology
Kleo, Karsten K; Jovanovic, Vladimir M VM; Arndold, Alexander A; Lehmann, Annika A; Lammert, Hedwig H; Berg, Erika E; Harloff, Hannah H; Treese, Christoph C; Hummel, Michael M; Daum, Severin S
Publication Date: 2022-03-05

Variant appearance in text: SPOCK1: 187-30594C>T; rs13182883
PubMed Link: 35246724
Variant Present in the following documents:
  • 432_2022_3944_MOESM1_ESM.xlsx, sheet 1
View BVdb publication page



Evaluation of OpenArray™ as a Genotyping Method for Forensic DNA Phenotyping and Human Identification.

Genes
Ragazzo, Michele M; Puleri, Giulio G; Errichiello, Valeria V; Manzo, Laura L; Luzzi, Laura L; Potenza, Saverio S; Strafella, Claudia C; Peconi, Cristina C; Nicastro, Fabio F; Caputo, Valerio V; Giardina, Emiliano E
Publication Date: 2021-02-03

Variant appearance in text: rs13182883
PubMed Link: 33546406
Variant Present in the following documents:
  • Main text
  • genes-12-00221.pdf
View BVdb publication page



Confirmation of Paternity despite Three Genetic Incompatibilities at Chromosome 2.

Genes
Doniec, Andrzej A; Łuczak, Wojciech W; Wróbel, Maria M; Januła, Miłosz M; Ossowski, Andrzej A; Grzmil, Paweł P; Kupiec, Tomasz T
Publication Date: 2021-01-04

Variant appearance in text: rs13182883
PubMed Link: 33406744
Variant Present in the following documents:
  • Main text
View BVdb publication page



The mutational load and a T-cell inflamed tumour phenotype identify ovarian cancer patients rendering tumour-reactive T cells from PD-1+ tumour-infiltrating lymphocytes.

British Journal Of Cancer
Salas-Benito, Diego D; Conde, Enrique E; Tamayo-Uria, Ibon I; Mancheño, Uxua U; Elizalde, Edurne E; Garcia-Ros, David D; Aramendia, Jose M JM; Muruzabal, Juan C JC; Alcaide, Julia J; Guillen-Grima, Francisco F; Minguez, Jose A JA; Amores-Tirado, Jose J; Gonzalez-Martin, Antonio A; Sarobe, Pablo P; Lasarte, Juan J JJ; Ponz-Sarvise, Mariano M; De Andrea, Carlos E CE; Hervas-Stubbs, Sandra S
Publication Date: 2021-03

Variant appearance in text: SPOCK1: 187-30594C>T; rs13182883
PubMed Link: 33402737
Variant Present in the following documents:
  • 41416_2020_1218_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



Genetic assessment reveals no population substructure and divergent regional and sex-specific histories in the Chachapoyas from northeast Peru.

Plos One
Guevara, Evelyn K EK; Palo, Jukka U JU; Översti, Sanni S; King, Jonathan L JL; Seidel, Maria M; Stoljarova, Monika M; Wendt, Frank R FR; Bus, Magdalena M MM; Guengerich, Anna A; Church, Warren B WB; Guillén, Sonia S; Roewer, Lutz L; Budowle, Bruce B; Sajantila, Antti A
Publication Date: 2020

Variant appearance in text: rs13182883
PubMed Link: 33382772
Variant Present in the following documents:
  • Main text
  • pone.0244497.pdf
View BVdb publication page



Inter-laboratory study on standardized MPS libraries: evaluation of performance, concordance, and sensitivity using mixtures and degraded DNA.

International Journal Of Legal Medicine
Müller, Petra P; Sell, Christian C; Hadrys, Thorsten T; Hedman, Johannes J; Bredemeyer, Steffi S; Laurent, Francois-Xavier FX; Roewer, Lutz L; Achtruth, Sabrina S; Sidstedt, Maja M; Sijen, Titia T; Trimborn, Marc M; Weiler, Natalie N; Willuweit, Sascha S; Bastisch, Ingo I; Parson, Walther W; ,
Publication Date: 2020-01

Variant appearance in text: rs13182883
PubMed Link: 31745634
Variant Present in the following documents:
  • Main text
  • 414_2019_Article_2201.pdf
View BVdb publication page



Qualitative and quantitative assessment of Illumina's forensic STR and SNP kits on MiSeq FGx™.

Plos One
Sharma, Vishakha V; Chow, Hoi Yan HY; Siegel, Donald D; Wurmbach, Elisa E
Publication Date: 2017

Variant appearance in text: rs13182883
PubMed Link: 29121662
Variant Present in the following documents:
  • Main text
  • pone.0187932.pdf
View BVdb publication page



Simultaneous genomic identification and profiling of a single cell using semiconductor-based next generation sequencing.

Applied & Translational Genomics
Watanabe, Manabu M; Kusano, Junko J; Ohtaki, Shinsaku S; Ishikura, Takashi T; Katayama, Jin J; Koguchi, Akira A; Paumen, Michael M; Hayashi, Yoshiharu Y
Publication Date: 2014-09-01

Variant appearance in text: rs13182883
PubMed Link: 27294018
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page



Allele frequencies for 40 autosomal SNP loci typed for US population samples using electrospray ionization mass spectrometry.

Croatian Medical Journal
Kiesler, Kevin M KM; Vallone, Peter M PM
Publication Date: 2013-06

Variant appearance in text: rs13182883
PubMed Link: 23771752
Variant Present in the following documents:
  • Main text
  • CroatMedJ_54_0225.pdf
View BVdb publication page